Chemist jobs in California

The Research Chemist will independently execute laboratory testing and research activities using chemical, physical, and advanced instrumental techniques to support the analysis and characterization of cementitious materials. This role is responsible for ensuring accurate data generation, interpretation, and reporting in accordance with ASTM, AASHTO, ACI, and other applicable standards, while supporting Technical Services, Operations, Quarry and R&D initiatives, maintaining laboratory safety and quality systems, and collaborating with cross-functional teams to deliver results from sample intake through project completion. CalPortland is proud to offer a comprehensive, competitive benefits package that provides health and financial support to our most important resources: our employees. Your benefits are an important part of your overall compensation at CalPortland. That’s why we give you a wide range of benefits to choose from. • Medical, Dental, Vision, • low-cost premiums even for family coverage, • Company-paid life/AD&D insurance, • Company-paid short-term disability, • Paid sick/vacation/holiday, • 401k/Company Funded Pension Program (program is dependent upon location and job type), • Employee Assistance Program (EAP), • Additional voluntary benefits, • Provide laboratory support for ongoing projects focused on the chemical analysis and characterization of cementitious materials. These efforts support multiple departments, including Technical Services, Operations, Quarry, and Research & Development., • Maintain laboratory safety at its highest standard. This includes but is not limited to; assessing the risks of any tasks before starting, only performing authorized tasks, utilizing proper PPE, and ensuring the company’s guidelines and policies are adhered to., • Conducts laboratory equipment troubleshooting, maintenance, and calibrations to meet or exceed all internal and external quality standards., • Prepare related documentation and reports by monitoring, analyzing and collecting data, i.e., XRF, XRD, Calorimetry reports, etc., • Conduct testing as per applicable (ASTM, AASHTO, ACI, EPA, etc.) test methods., • Evaluate laboratory needs; equipment, testing, and quality requirements to ensure accurate analytical testing as required for projects., • Support the Laboratory Manager and Project Coordinator in daily Central Laboratory operations, while assisting other work areas to ensure project deadlines are met., • Assist with the laboratory’s lean and housekeeping activities, • BS Degree in Chemistry, Geology, Material Science; or Engineering, Chemistry, or a related field, with a minimum of 5 years of relevant experience, • Other degrees may be acceptable depending on work experience, • In-depth knowledge and expertise of cement and concrete materials with respect to current ASTM, AASHTO, and ACI standards., • Strong hands-on experience with testing methods and analytical techniques for cementitious materials, such as XRF, XRD, LOI, Blaine fineness, density, insoluble residue, free lime, ICP, isothermal calorimetry, and related procedures. Minimum 5 years of successful laboratory work, • Must have strong math, physics, and analytical understanding., • Strong written and verbal communications skills, • Well-versed in Microsoft Office applications (i.e., Outlook, Word, Excel, SharePoint, and Planner), • Strong understanding of ASTM and ACI specifications, • Interpersonal skills to facilitate working relationships with all levels of management and staff Successful candidate must submit to a post-offer pre-employment physical examination, drug/alcohol screen, and background check. Some positions require Federal Motor Carrier Safety Administration (FMCSA) registration/clearance as well as ongoing alcohol and drug testing. In accordance with the San Francisco Fair Chance Ordinance, for work that will be performed in the San Francisco area, qualified applicants with arrest and conviction records will be considered for employment.

Job Description Job Description: Onsite Position Summary: The Company has an opportunity in the Advanced Measurement Sciences (AMS) Analytical Group at our Research and Development Center in Pleasanton, California for an experienced Contract Lab Chemist (Technician). As a Contractor Technician in the AMS Analytical group, you will be part of a team growing numerous brands across the portfolio, including Burts Bees, Kingsford, Hidden Valley, Pine-Sol, Brita and others. Through collaboration with Scientists in the group and inter-functionally between groups, you will look to help create over $150MM of value per year. Daily responsibilities include product and material analysis, method development and data analysis for a variety of products, focusing on those specifically from the Cleaning and Professional Products Divisions. You will work closely with Scientists to provide reports, identify issues and recommend next steps based on experimentation. You will also have the opportunity to take on non-project specific initiatives within the department to increase the knowledge base and functionality of the group as a whole. We require someone with direct hands-on experience and expertise in any of the following: Working in a regulated lab environment such as GLP, GMP, and with EPA/FDA GLP or GMP method validation and product characterization. Responsibility for analytical instrument method development, maintenance, supplies, repairs, purchases, and analyses, for various project teams. Various wet chemistry techniques including standard sample preparation methodologies such as accurate weighing, pipetting, centrifugation, dilution, extraction, drying and characterization methodologies such as pH adjustment, titration, moisture content, extraction, or drying; expertise in the preparation and use of calibration standards and controls. Spectroscopy techniques such as with UV/VIS or fluorescence instrumentation. Chromatography instruments (LC, GC, IC), related detectors, software programs, and techniques for compound identification and quantitation. Chemical and biochemical assay development, optimization, transfer, validation. Experience in analyzing a variety of raw materials, process intermediates, and finished products in the following consumer goods industries is highly desired: Household and institutional cleaning products, personal care, foods, charcoal, litter, water filtration, nutraceuticals, and probiotics. Demonstrated knowledge of statistical analysis. Ability to summarize and report analytical results, perform trend analysis, and implement corrective action as needed. Strong willingness and aptitude to learn and master new tools and skills. Experience in working collaboratively with multi-functional teams in a fast-paced environment, and in providing guidance/training for others on routine assignments. Ability to multi-task and manage work efforts on multiple projects according to assigned priorities. Excellent adherence to lab and chemical safety requirements, company documentation policies, and a strong demonstrated work ethic. Key Responsibilities (in descending order of importance): Accurately follow assay and safety procedures, and SOPs. Perform reliable sample preparation and analytical testing in the lab using various analytical chemistry techniques. Optimize sample preparation and analytical methodologies as needed. Operate related equipment and software under peak performance and safety conditions. Maintain equipment and software, upgrading and making purchase recommendations for new capabilities as necessary. Process and report analytical data using instrument software, Microsoft Excel, Word, and PowerPoint. Knowledge of Outlook, Microsoft Teams, and SharePoint preferred. Accurately and promptly instrument log data and lab activities in log or lab notebooks. Present data to project team members and management: The ability to promptly communicate plans and explain results is a must. Well-developed writing and speaking skills are required. Participate in general lab management for the wet chemistry lab such as in maintaining an organized, clean and safe lab environment/workspace, ordering supplies, maintaining or repairing instrumentation, performing calibrations, keeping instrument, and chemical inventory records. Minimum Requirements: Years and Type of Experience: 3-5+ years experience working in an analytical chemistry lab in a consumer goods, chemicals, crop protection, pharmaceutical company, or contract research organization. Education Level/Degree: B.Sc. in Chemistry, Biochemistry, or related scientific field. Requirements: Key Responsibilities (in descending order of importance): Accurately follow assay and safety procedures, and SOPs. Perform reliable sample preparation and analytical testing in the lab using various analytical chemistry techniques. Optimize sample preparation and analytical methodologies as needed. Operate related equipment and software under peak performance and safety conditions. Maintain equipment and software, upgrading and making purchase recommendations for new capabilities as necessary. Process and report analytical data using instrument software, Microsoft Excel, Word, and PowerPoint. Knowledge of Outlook, Microsoft Teams, and SharePoint preferred. Accurately and promptly instrument log data and lab activities in log or lab notebooks. Present data to project team members and management: The ability to promptly communicate plans and explain results is a must. Well-developed writing and speaking skills are required. Participate in general lab management for the wet chemistry lab such as in maintaining an organized, clean and safe lab environment/workspace, ordering supplies, maintaining or repairing instrumentation, performing calibrations, keeping instrument, and chemical inventory records. Minimum Requirements: Years and Type of Experience: 3-5+ years experience working in an analytical chemistry lab in a consumer goods, chemicals, crop protection, pharmaceutical company, or contract research organization. Education Level/Degree: B.Sc. in Chemistry, Biochemistry, or related scientific field.

Job DescriptionJob Title: Senior Scientist I/II, Analytical Chemistry Job Description We are seeking a highly experienced analytical chemist to lead unknown compound identification and Extractables & Leachables (E&L) studies for pharmaceutical and medical device products. This role requires deep expertise in LC/MS, method development, and structural elucidation. Responsibilities • Identify unknown compounds using LC/MS, LC-MS/MS, and LC-HRMS., • Develop, optimize, and troubleshoot analytical methods., • Analyze and interpret complex mass spectrometry data., • Support pharmaceutical and medical device E&L studies., • Prepare technical reports, protocols, and regulatory documentation., • Collaborate with cross-functional teams to solve analytical challenges., • Mentor junior scientists and provide technical guidance., • Evaluate and implement new analytical technologies and methodologies.Essential Skills, • Ph.D. in Analytical Chemistry or related field., • 5+ years of experience in LC/MS and unknown compound identification., • Strong expertise with high-resolution mass spectrometry (LC-HRMS)., • Experience in pharmaceutical, medical device, or CRO environments., • Strong background in organic chemistry and structural elucidation., • Knowledge of ESI and MS/MS techniques., • Familiarity with GLP, GMP, ISO -18, USP <1663>, and USP <1664>., • Strong communication, problem-solving, and leadership skills.Additional Skills & Qualifications, • Experience with Sciex OS, Thermo Orbitrap/Chromeleon, or GC/MS is a plus.Work Environment This position requires onsite presence five days a week in Hercules. The work environment is dynamic, providing opportunities to solve complex analytical challenges in the life sciences industry. Job Type & Location This is a Contract to Hire position based out of Hercules, CA. Pay and Benefits The pay range for this position is $55.28 - $64.90/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Hercules,CA. Application Deadline This position is anticipated to close on Jul 23, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job DescriptionJob Title: Analytical Chemist Job Description This bench-focused Analytical Chemist role centers on hands-on work in a regulated laboratory, performing analytical testing with HPLC and LC-MS to support product, process, and quality-related studies. You will prepare samples and reagents, operate and maintain analytical instruments, generate and interpret data, and ensure all activities comply with GMP, GLP, and established laboratory procedures. The position suits someone with 1–2 years of direct industry experience who enjoys working in a fast-paced, collaborative wet lab environment and contributing to high-quality scientific outcomes. Responsibilities • Perform routine analytical testing using HPLC and LC-MS methods to support product, process, and quality-related studies., • Prepare samples, reagents, calibration standards, and mobile phases in accordance with SOPs and approved methods., • Operate, maintain, and perform basic troubleshooting of HPLC and LC-MS systems to ensure reliable performance., • Execute analytical assays and experiments following validated methods and established protocols., • Analyze chromatographic and mass spectrometry data and accurately document results in approved formats., • Record experimental activities and results in laboratory notebooks, LIMS, or other controlled documentation systems., • Support instrument qualification, calibration, and preventative maintenance activities as assigned., • Maintain strict compliance with GMP, GLP, and laboratory safety requirements at all times., • Assist with method transfers, SOP revisions, and laboratory investigations as needed to support ongoing projects., • Collaborate with scientists and cross-functional teams to support project timelines and deliverables., • Contribute to maintaining clean, organized, and audit-ready laboratory workspaces., • Participate in continuous improvement of analytical methods, workflows, and documentation practices where appropriate.Essential Skills, • B.S. degree in Chemistry, Biochemistry, Analytical Chemistry, or a related scientific discipline., • Minimum 1–2 years of direct industry experience operating HPLC and LC-MS instrumentation in a regulated laboratory environment., • Demonstrated experience with sample preparation, instrument setup, sequence creation, data review, and basic troubleshooting., • Hands-on experience performing analytical testing using HPLC and LC-MS methods., • Experience working in a GMP, GLP, pharmaceutical, biotech, food, environmental, or contract research (CRO) laboratory environment., • Familiarity with chromatography data systems and electronic or paper-based laboratory documentation practices., • Strong attention to detail with the ability to follow SOPs and maintain accurate, complete, and compliant records., • Ability to manage multiple priorities and deliver high-quality work in a fast-paced laboratory setting., • Solid understanding of laboratory safety practices and regulatory expectations in a GMP/GLP environment., • Strong communication and collaboration skills to work effectively with scientists and cross-functional teams.Additional Skills & Qualifications, • Experience with method qualification, verification, or validation activities., • Exposure to additional analytical techniques such as GC, ICP-MS, UV-Vis, or dissolution testing., • Experience with ELISA platforms or other complementary analytical systems., • Previous experience supporting quality control, manufacturing support, or product development programs., • Experience participating in instrument qualification, calibration, and preventative maintenance programs., • Comfort working with LIMS or other controlled documentation systems in a regulated environment., • Demonstrated ability to contribute to SOP revisions, method transfers, or laboratory investigations., • Interest in continuous improvement of laboratory workflows, data integrity, and documentation standards.Work Environment This role is fully onsite in a bench-based wet laboratory environment five days a week. You will work in a regulated GMP/GLP setting that emphasizes safety, quality, and compliance in all activities. The position involves extensive hands-on work with analytical instruments such as HPLC, GC, LC-MS, ICP-MS, ELISA platforms, UV-based systems, and related laboratory equipment. You will routinely handle reagents, samples, and standards while maintaining clean, organized, and audit-ready workspaces. The laboratory operates in a fast-paced, highly collaborative atmosphere where clear communication, adherence to established procedures, and meticulous documentation are essential. The environment supports close teamwork with scientists and cross-functional partners, with a strong focus on reliability, data integrity, and continuous improvement in analytical practices. Job Type & Location This is a Contract to Hire position based out of Hercules, CA. Pay and Benefits The pay range for this position is $30.00 - $35.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Hercules,CA. Application Deadline This position is anticipated to close on Jul 23, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description SUMMARY DESCRIPTION The Formulation Chemist is responsible for the research, design, and development of innovative personal care and home care products, including skincare, haircare, body care and laundry, dish, and surface cleansers. Working in a fast-paced contract manufacturing environment, you will translate customer briefs into commercially viable products while ensuring stability, safety, and regulatory compliance. PERFORMANCE EXPECTATIONS • Product Development: Create new formulations from scratch and improve existing ones to meet client specifications. • Bench-to-Production Scale-Up: Oversee the transition from small lab batches to pilot plant and full-scale manufacturing trials. • Stability & Compatibility Testing: Conduct rigorous testing to ensure product integrity under varying temperatures and confirm compatibility with packaging. • Technical Troubleshooting: Identify and resolve batching or quality issues during the manufacturing process to ensure Right-The-First-Time production. • Raw Material Management: Collaborate with suppliers to source innovative ingredients and identify cost-effective alternatives. • Documentation: Maintain detailed lab notebooks and prepare technical documents in compliance with cGMP and FDA standards. • Client Collaboration: Interface with sales and marketing teams to provide technical insights and updates for client projects. • Perform other regulatory compliance-related activities as assigned. MEETING PARTICIPATION • Any as requested. AUTHORITY This position reports to the VP of Research & Development. CLASSIFICATION This is a full-time exempt role. Your primary office location will be the Company’s Watsonville, CA headquarters. The Company reserves the right to reasonably require you to perform your duties at places other than your primary office location from time to time, and to require reasonable business travel. EDUCATION • Bachelor’s degree with a Chemistry, Chemical Engineering, Cosmetic Science, or a related field. WORK EXPERIENCE • Minimum of 3–5 years of hands-on formulation experience in the personal care, home care or beauty industry, preferably within a contract manufacturing setting. OTHER QUALIFICATIONS • Laboratory Operations: Intimate knowledge of laboratory practices, safety compliance, and management and handling hazardous chemicals. • Regulatory Knowledge: Familiarity with global cosmetic regulations and Good Manufacturing Practices (GMP). • Soft Skills: Strong analytical problem-solving, project management skills to juggle multiple client projects, and excellent communication. WORKING ENVIRONMENT • This is an on-site position based in a laboratory and manufacturing facility., • The role involves handling various raw materials and chemicals, requiring strict adherence to safety protocols and the use of Personal Protective Equipment (PPE).

Job DescriptionCompany Description ABOUT LGC BIOSEARCH TECHNOLOGIES: With manufacturing sites across the US, UK, Germany and Denmark, LGC Biosearch Technologies has plans to continue growing. We deliver mission critical genomics to our diverse customer base in molecular diagnostics, pharma/biotech and agrigenomics. Our integrated portfolio of products, services and expertise supports our purpose of Science for a Safer World and we have embodied our mission by working with customers to enable research into life-altering treatment for disease and illness worldwide. We are currently seeking candidates who are up for the challenge of operating in a high-growth, purpose-driven organisation. Job Description Principal Oligonucleotide Chemist Company: LGC Biosearch Technologies Location: 2100 South McDowell, Petaluma, CA 94952 Type: Full‑time Company Overview LGC Biosearch Technologies operates across manufacturing sites in the US, UK, Germany, and Denmark, providing mission‑critical genomics solutions to customers in molecular diagnostics, pharma/biotech, and agrigenomics. Our integrated portfolio of products, services, and expertise supports our mission of Science for a Safer World. We partner closely with customers to enable research and development of life‑altering treatments for diseases worldwide. Join our high‑growth, purpose‑driven organization. Position Summary The Principal Oligonucleotide Chemist is a senior scientific leader responsible for driving oligonucleotide product development, synthesis, process development, and innovation across the Innovation Hub, operations, and customer‑facing programs. This role blends hands‑on laboratory execution with strategic experimental design, data‑driven development, project leadership, and mentorship of scientists to deliver new products. You will serve as the technical lead for Oligonucleotide New Product Development (NPD), and Customer co‑creation product projects, designing new manufacturing methods, troubleshooting complex issues, supporting tech transfer, and presenting technical content to commercial teams and customers. This position plays a critical role in advancing LGC’s oligonucleotide chemistry capabilities and new product offerings. Key Responsibilities Leadership in Oligonucleotide Chemistry, Project Execution and Delivery • Lead Petaluma Innovation Hub Oligo Chemistry Function by delivering customer co‑creation and NPD products/projects from concept through delivery., • Partner with peers and global team to deliver to customers and achieve Innovation Hub development and financial objectives., • Serve as a technical lead for multi-site, multi-function development team for oligonucleotide synthesis, modification, deprotection, purification, and analytical characterization., • Participate in evaluation of new technologies and oligonucleotide market strategy, • Oversee and Execute oligo synthesis projects, including experimental design/planning, prioritization, and resource coordination., • Deliver and control new methods, workflows, and manufacturing protocols for oligonucleotide synthesis, purification and analysis. Support operations technically., • Optimize, and define manufacturing instructions for low‑yielding or impure processes. Laboratory Execution & Product Manufacturing • Lead projects and staff hands-on in the lab by performing and training synthesis and purification of oligonucleotides using automated and manual techniques., • Conduct analytical characterization (LC‑MS, HPLC, CE, UV‑Vis) to confirm identity, purity, and impurity profiles., • Troubleshoot synthetic routes, instrument performance, and purification workflows and analytics to ensure consistent, high‑quality output., • Develop and refine synthetic routes, synthesis method refinement, coupling conditions, deprotection strategies and purification methods. Experimental Design, Data Analysis & Development Strategy • Design rigorous, data‑driven experiments to optimize yield, purity, scalability (up and down), and process robustness., • Use mechanistic understanding and statistical analysis to adjust development plans and guide next‑step decision‑making., • Lead troubleshooting efforts by designing investigation maps and structured experimental plans., • Document experimental results, conclusions, and recommendations by industry standard technical summary reports and within quality certification requirements. Customer Co‑Creation & Technical Communication • Successfully lead and deliver oligonucleotide customer co‑creation and NPD projects., • Participate in technical customer calls related to custom oligo manufacturing, product investigations, and development updates., • Present technical content to commercial teams and customers, including data reviews, capability overviews, and project progress. Operations Support, Tech Transfer & Continuous Improvement • Provide technical support to Operations for process optimization, scale‑up, and continual improvement., • Lead the successful transfer of custom product methods and procedures into MSAT and Operations teams., • Develop effective tech transfer plans and verify training for newly developed processes., • Deliver method validation in alignment with Quality department requirements., • Support troubleshooting and root‑cause investigations for manufacturing challenges. Mentorship & Team Development • Mentor and develop scientists in oligonucleotide chemistry; providing guidance in technical skills, experimental design, and professional development., • Promote rigorous laboratory order and management, controlled documentation, and best practices in experimental execution., • Foster a collaborative, trust building and growth‑oriented environment that supports scientific excellence. Technical Skills • Proven expertise in oligonucleotide chemistry., • Demonstrated knowledge of solid‑phase oligonucleotide synthesis and modification., • Skilled in analytical characterization of oligonucleotides, including impurity profiling., • Demonstrated project management skills with experience leading matrixed teams through complex development projects. Seasoned ability to design, optimize, and troubleshoot oligonucleotide manufacturing development processes Qualifications Qualifications • Ph.D. in Synthetic Organic Chemistry, Chemical Biology, or related field inclusive of extensive experience in oligonucleotide chemistry., • Minimum of 15 years of direct industry experience in oligonucleotide synthesis, product and process development, and tech transfer into manufacturing., • Demonstrated ability to lead technical projects, mentor scientists, and collaborate cross‑functionally., • Excellent communication skills, including the ability to present complex technical content to internal and external audiences. Additional Information The typical pay range for this role is: Minimum: $ 131,155/ Annualy Maximum: $196,733/ Anually This range represents the low and high end of the anticipated salary range for the California -based position. The actual base salary will depend on several factors such as: experience, skills, and location. ABOUT LGC: LGC is a leading, global life science tools company, providing mission-critical components and solutions into high-growth application areas across the human healthcare and applied market segments. Its high-quality product portfolio is comprised of mission-critical tools for genomic analysis and for quality assurance applications, which are typically embedded and recurring within our customers’ products and workflows and are valued for their performance, quality, and range. OUR VALUES • PASSION, • CURIOSITY, • INTEGRITY, • BRILLIANCE, • RESPECT EQUAL OPPORTUNITIES LGC strongly believes that every job applicant and employee should be valued for their individual talents regardless of age, disability, race, color, ethnic or national origin, sex, sexual orientation, gender reassignment, marital or civil partnership, pregnancy or maternity, religion, or belief. Short listing, interviewing and selection will always be carried out without regard to gender, sexual orientation, marital status, color, race, nationality, ethnic or national origins, religion or belief, age, or trade union membership. For more information about LGC, please visit our website www.lgcgroup.com #scienceforasaferworld

Job DescriptionCompany Description Veolia has acquired Clean Earth. As Clean Earth completes its integration into Veolia, recruiting and hiring for this role is being managed in partnership with the Clean Earth talent acquisition team. Veolia in North America is the top-ranked environmental company in the United States for three consecutive years, and the country’s largest private water operator and technology provider as well as hazardous waste and pollution treatment leader. It offers a full spectrum of water, waste, and energy management services, including water and wastewater treatment, commercial and hazardous waste collection and disposal, energy consulting and resource recovery. Veolia helps commercial, industrial, healthcare, higher education and municipality customers throughout North America. Headquartered in Boston, Veolia has more than 10,000 employees working at more than 350 locations across North America. Job Description PRINCIPAL DUTIES AND RESPONSIBILITIES: • Handles hazardous materials including inventorying, identifying, segregating, and packaging waste material in accordance with Lab Pack policies, procedures and practices and all applicable regulations., • Perform onsite services which may include waste collection, consolidation (i.e., bulking, repackaging), sampling, safety/compliance inspections, and other related activities required by the customer/contract. Assists other business groups, i.e., Depack, Retail and HHW, both internal and onsite as needed., • Preparing shipment of packaged waste by inspecting, labeling, marking, and loading into the transport vehicle., • Properly completes documentation including shipping papers, Land Disposal Restrictions (LDR’s), evaluations/certifications and other required documentation in accordance with appropriate regulations and procedures., • Maintain a Commercial Driver’s License (CDL) with Hazmat Endorsement to legally operate Clean Earth vehicles necessary for transporting personnel and waste to and from customers’ job locations., • Follows, understands, and promotes by example, all Health & Safety /Job Safety Analysis (JSA’s) procedures including development of on-site Health &Safety plans/JSA’s as outlined in the procedures and policies., • Perform unknown field testing for classification and packaging for transportation and disposal., • Mentor and assist new employees in field work duties., • Complete site walks to inventory and assess requirements for potential and awarded work., • Assist sales in creating estimates for lab pack work., • Lead/coordinate field service/lab pack jobs requiring multiple personnel/days., • Assist in other areas as directed including but not limited to assistance in scheduling and support of staff training., • Performs other duties as assigned Pay range $37.00 - $38.00 hourly. Qualifications Basic Requirements: • Associate College in general science (BS preferred) is required for the Lab Pack Chemist., • Commercial Driver’s License (CDL) with Hazardous Material endorsement and a clear record, • Moderate to extensive travel with 20% overnight travel, • Physical ability to lift and move material of various weights frequently exceeding 55 lbs, • Basic understanding of chemistry through general chemistry or biology, • Advanced knowledge of EPA and DOT, • Minimum two (2) years lab pack experience, • 40-hour OSHA HAZWOPER, • 8 hours DOT Training, • PPE Training which includes Respirators, • 40 hours Depack Experience This position requires a CDL B to be obtained within a 6-month period from your start date. Failure to obtain a CDL B within the 6-month period will mean you are no longer eligible for the Lab Pack Chemist position. This position is also contingent upon successful completion of a DOT physical, DOT Drug Screen and any other DOL or company requirements. Additional Information Benefits: Comprehensive benefits package includes paid time off policies, as well as health, dental, vision, life insurance, tuition reimbursement, paid volunteering and more. In addition, commencing no later than January 1, 2027, benefits package will include participation in an employer sponsored 401(k) plan, to save for retirement. Pay and benefits for employees represented by a union are outlined in their collective bargaining agreement. We are an Equal Opportunity Employer! All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Disclaimer: The salary, other compensation, and benefits information is accurate as of the date of this posting. The Company reserves the right to modify this information at any time, subject to applicable law

Job Description We have an open METHOD VALIDATION / ANALYTICAL CHEMIST III position in our Quality Control Department in the Irvine, CA location. PRIMARY DUTIES AND RESPONSIBILITIES: • Perform method validation, verification, transfer, analytical testing for clinical submission materials, including raw materials, finished products, stabilities and cleaning validation., • Maintain and troubleshoot analytical instrumentation., • Perform and document laboratory investigations, as necessary., • Peer review data generated by other chemists and technicians., • Develop, validate and troubleshoot analytical methods., • Conduct method transfers from other facilities and departments., • Author standard operating procedures and analytical methods., • Perform and/or assist with equipment calibrations and qualification., • Assist laboratory management with laboratory employee training., • Assist laboratory management in preparation for internal, customer and agency audits., • Other related duties as required. QUALIFICATIONS: • Bachelor's degree in chemistry or related discipline., • 5+ years' experience in a chemistry laboratory, or equivalent combination of education and experience., • 5+ years' experience with analytical instrumentation, such as HPLC, GC, CE, ICP, FTIR, and dissolution apparatus required., • 2+ years' experience in GLP or GMP (preferred) environment., • Ability to follow standard operating procedures., • Strong communication skills, both written and verbal., • Ability to organize, prioritize and effectively perform concurrent tasks with minimal supervision., • Strong attention to detail. At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity employer. All suitably qualified candidates will receive consideration for employment based on objective work-related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws.

Job DescriptionSalary: $21-$22/hourly DOE POSITION SUMMARY: Perform qualitative and quantitative chemical and physical analysis of raw materials and dietary supplement finished products in the Quality Control Laboratory using wet chemistry techniques and analytical instrumentation. This position reports to Quality Control Laboratory Operations Supervisor. MAJOR FUNCTIONS & RESPONSIBILITIES: • Perform qualitative and quantitative chemical and physical analysis of raw materials and finished products., • Prepare standards and reagents; calibrate and operate simple as well as sophisticated laboratory instruments such as pH-meter, refractometer, scale, titrator, viscometer, FTIR spectrophotometer, UV-Vis spectrophotometer, and HPLC., • Document analytical data in laboratory notebook and follow Good Laboratory Practices, Good Documentation Practices and Good Manufacturing Practices., • Review product certificates of analysis for accuracy and conformance., • Solve practical problems and carry out responsibilities under general supervision., • Order laboratory supplies, and maintain a safe, clean and efficient laboratory., • Properly file all documents related to the received raw materials, packaging components and labels for easy retrieval., • Properly manage raw material reserve samples collection and storage., • Participate in the release of staged raw materials., • Other responsibilities as determined and assigned by the Quality Control Laboratory Operations Manager., • Follow all applicable safety and standard guidelines such as companys SOPs, cGMP, Good Documentation Practices and/or Good Laboratory Practices. REQUIRED EDUCATION / WORK EXPERIENCE / SKILLS: • BS degree in Chemistry or related field with 0-2 years of relevant laboratory work experience in a Nutraceutical / Dietary Supplement or Pharmaceutical environment., • Experience in various wet chemical analysis and instrumentation using NIR spectrophotometer; experience with USP/FCC Methods is essential., • Must be a self-starter., • Ability to read and write English., • Basic computer knowledge (Excel and Word)., • Ability to stay focused and alert; utilize basics math skills; audit paperwork; carry out routine tasks with appropriate follow-up., • Team player, willing to assist others in their areas to accomplish the task., • Must be able to work overtime and week-ends as necessary. OTHER REQUIREMENTS: • Technical Skills - Excellent understanding of analytical chemistry and instruments. Pursue training and development opportunities; strive to continuously build knowledge and skills; share expertise with others., • Quality - Demonstrate accuracy and thoroughness; look for ways to improve and promote quality; apply feedback to improve performance; monitor own work to ensure quality., • Teamwork - Balance team and individual responsibilities; exhibit objectivity and openness to others' views; give and welcome feedback; contribute to building a positive team spirit; put success of team above own interests; support everyone's efforts to succeed., • Quantity - Meet productivity standards; complete work in timely manner; strive to increase productivity; work quickly., • Leadership - Exhibit confidence in self and others; inspire and motivate others to perform well; effectively influence actions and opinions of others; accept feedback from others; give appropriate recognition to others., • Analytical - Synthesize complex or diverse information; collect and research data; use intuition and experience to complement data; design work flows and procedures., • Organizational Support - Follow policies and procedures; complete administrative tasks correctly and on time; support organization's goals and values., • Safety and Security - Observe safety and security procedures; determine appropriate action beyond guidelines; report potentially unsafe conditions; use equipment and materials properly.

Job Description RESPONSIBILITIES: • Perform and/or assist with analytical testing of raw materials, in-process samples, and finished products., • Utilize analytical laboratory instrumentation with minimal supervision., • Comply with cGMP regulations and follow all standard operating procedures., • Peer review data generated by other technicians., • Maintain and troubleshoot laboratory equipment and analytical instrumentation within level of experience., • Perform and/or assist with equipment calibrations and qualifications., • Other related duties as required. QUALIFICATIONS: • Bachelor's degree in chemistry or related discipline., • 2-5 years’ experience in a pharmaceutical chemistry laboratory., • 2- 5 years’ experience with analytical instrumentation, such as HPLC, GC, CE, ICP, FTIR, TOC, MS, and dissolution apparatus., • Ability to follow standard operating procedures., • Strong communication skills, both written and verbal., • Ability to organize, prioritize and effectively perform concurrent tasks with minimal supervision., • Strong attention to detail. At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity employer. We offer medical, dental, vision and company matching 401K. All suitably qualified candidates will receive consideration for employment based on objective work-related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws.

Job Description Production ChemistThis is an exciting opportunity to join a global, industry leading company. The Chemist will formulate products and intermediates utilizing biologicals and chemicals of varying properties and characteristics in order to meet specificationsResponsibilities: • Responsible for bulk formulating products of low to medium complexity including intermediates in accordance with approved written procedures and policies., • Perform data entry and inventory control utilizing the ERP database., • Responsible for completing production documentation and maintaining quality records to GDP/GMP standards., • Coordinate prioritize and plan lab tasks to meet strict deadlines., • Follows controlled Standard Operation Procedures/ documents., • Monitors manufacturing processes and performs adjustments when necessary to meet required yields. Requirements and Desired Experience:, • Bachelor’s degree in a life science or related field, • 0-3 years working in a general manufacturing environment formulating products in the areas of biological sciences, life sciences, or an equivalent., • Ability to follow guidelines and handle hazardous materials safely., • Ability to work in a product team and make decision of limited scope, subject to review., • Able to follow detailed procedures and have good documentation skills. Understanding of Good Manufacturing Practices and Good Laboratory Practices., • Must be experienced in using ERP systems- SAP a plus., • Working knowledge of Microsoft Office tools – Excel and Word., • Basic working knowledge of laboratory environments, materials, and equipment.Pay Range (Based on Experience & Qualifications): $31 per hour

Job Description Certified Group is committed to partnering with customers to deliver innovative scientific solutions and expertise – So The World Can Trust In What It Consumes™. Our network of 30+ North American and European laboratories serves the food & beverage, dietary supplements, cosmetics, OTC, tobacco/nicotine, cannabis, and hemp industries. Our Brands Certified Group is comprised of a set of specialized brands that collectively deliver laboratory testing, regulatory consulting, and certification & audit services across highly regulated industries: • Certified Laboratories – Provides comprehensive analytical and microbiological testing, primarily supporting food, beverage, cosmetics, OTC, and dietary supplement industries., • Food Safety Net Services (FSNS) – A leading network of ISO-accredited laboratories across North America, focused on food safety testing, operational support, and technical services for the food industry., • Labstat – A global leader in contract research and testing for nicotine, tobacco, cannabis, hemp, and next-generation products, with deep expertise in analytical chemistry and toxicology., • EAS Consulting Group – A regulatory consulting firm offering expert guidance, training, and auditing support across FDA, USDA, and other regulated sectors, powered by a large network of independent advisors., • FSNS Certification & Audit – Provides accredited third-party auditing and certification services, including food safety, animal welfare, and GMP programs. Certified Group is committed to delivering expert solutions and quality testing our customers can feel confident in – on time, every time – so the world can trust in what it consumes. As a leading North American provider of laboratory testing, regulatory consulting, and certification & audit services, Certified Group includes Food Safety Net Services (FSNS), FSNS Certification & Audit, Certified Laboratories, EAS Consulting Group, and Labstat International Inc. Certified Group provides analytical testing and regulatory guidance services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, personal care, tobacco, nicotine, cannabis, and hemp industries. We have embarked on an important journey to unify and strengthen our culture by living these core values: Start with the Customer, Drive to Deliver, Commit to Safety and Quality, and Believe in the Team — including believing in you. We are currently looking for an Chemist to join our growing team! ESSENTIAL RESPONSIBILITIES • Perform analysis using one or more of the following techniques: GC, LCMS, GCMS, GC, HPLC, ICP/MS, ICP-OES, UV-VIS, FTIR, Titration, Gravimetric Analysis, or other techniques, as appropriate in a timely fashion maintaining a high level of quality., • Prepare analytical standards., • Perform daily balance, temperature and monthly pipette verification., • Perform sample processing in accordance with standard operating procedures., • Perform sample preparation., • Successfully participate in proficiency testing., • Calibrate and maintain analytical instruments., • Participate in relevant ISO QA/QC activities and documentation thereof, • Prepare standards and maintain inventory., • Effectively participate in proficiency testing as required by ISO17025 and other accrediting/certifying bodies., • Maintain analytical and quality records as required for accreditation/certification and related to analytical work and instrument maintenance., • Submit accurate and timely reports based on the analysis., • Identify results that require further investigation or discussion with the Department Manager/Supervisor., • Participate in OOS investigation and/or CAPA when necessary., • Plan and perform work to meet deadlines and expected turn-around times., • Perform routine diagnosis, troubleshooting and maintenance of equipment., • Learn new techniques and technologies as appropriate., • Works effectively with other departments., • Provide training to new chemists when needed., • Other duties as required. MINIMUM QUALIFICATIONS • BA/BS degree in Chemistry related field, or 2-3 year of relevant work experience, • Knowledge of GMP GLP GDP, • Strong relevant quantitative skills, • High level of computer skills and familiarity with data acquisition software, • Strong trouble-shooting and problem-solving skills, • High level of computer literacy, • Good conceptual basis in analytical chemistry, • Proven ability to perform standard chemical laboratory techniques Benefits: • Progressive 401k Retirement Savings Plan, • Employer Paid Short- Term and Long-Term Disability, and Life Insurance, • Group Medical, • Tuition Reimbursement, • Flexible Spending Accounts, • Dental, • Paid Holidays and Time Off, • Many positions which qualify for the company bonus program Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status. Schedule: Monday - Friday, 8:00AM - 5:00PM The compensation details provided below reflect the expected pay range for this role, based on the selected compensation structure and applicable guidelines. Actual pay within this range may vary depending on factors such as experience, skills, qualifications, and geographic location. Additional components of total rewards—such as bonuses, benefits, or incentives—may also apply where applicable. Salary Range for Pay Transparency$25—$28 USD By applying, you acknowledge that Certified Group will process your personal information for recruitment and hiring purposes in accordance with our Applicant Privacy Policy. California residents may review additional information about how we collect and use personal information, including retention and rights, in our California Notice at Collection. To view our Privacy Policy, click the link here: Certified Group Privacy Policy We are an Equal Opportunity Employer and make employment decisions without regard to protected characteristics under applicable law.

Job Description Research & Development Chemist Location: Oceanside, CA (On-Site) Schedule: Monday-Friday, 8:00 AM-5:00 PM Employment Type: Full-Time, Salaried Join a Company That's Building Something Different At CitroTech, we're redefining wildfire prevention through innovative, environmentally responsible fire protection technologies. Our products help protect communities, critical infrastructure, and natural resources while minimizing environmental impact. We're a startup with the momentum of a recently publicly traded company, and we're growing quickly. Our team is developing the next generation of fire protection chemistry, and we're looking for scientists who enjoy solving difficult technical problems with real-world impact. At CitroTech, research doesn't happen in isolation. The work you do in the laboratory quickly becomes manufacturing processes, customer solutions, regulatory submissions, and commercial products. If you're excited by the opportunity to develop chemistry that makes a measurable difference, we'd love to meet you. Does This Sound Like You? You enjoy solving problems that don't have obvious answers. You're naturally curious and thrive in a fast-paced environment where every day presents a new technical challenge. You don't get discouraged when experiments don't produce the expected results, you use the data to refine your approach and move forward. You enjoy working collaboratively, thinking critically, and balancing scientific rigor with practical manufacturing considerations. Rather than following a fixed research program, you're excited by the opportunity to develop new products, improve existing formulations, and help bring them successfully into production. Most importantly, you're comfortable in a startup environment where priorities evolve, timelines move quickly, and your ability to think on your feet is just as valuable as your chemistry knowledge. What You'll Do Working closely with the R&D team, you'll help develop, optimize, and commercialize innovative fire protection products from concept through manufacturing. Responsibilities include: • Design, execute, and analyze laboratory experiments to support new product development, • Develop and optimize chemical formulations through systematic experimental design, • Perform wet chemistry involving aqueous formulations, organic salts, corrosion inhibitor systems, and related specialty chemicals, • Investigate technical challenges through rapid problem-solving and root cause analysis, • Optimize manufacturing and mixing processes for successful production scale-up, • Conduct basic stability studies and interpret results, • Collaborate closely with manufacturing to troubleshoot production issues and continuously improve manufacturing processes, • Work with external laboratories to design testing programs, interpret results, and refine formulations based on testing outcomes, • Maintain accurate laboratory notebooks and technical documentation, • Prepare technical reports and communicate findings to the R&D team and leadership, • Support product validation and scale-up from laboratory through commercial manufacturing, • Assist with regulatory activities involving agencies such as the EPA, USDA, and other applicable regulatory bodies, • Review scientific literature, patents, and emerging technologies to identify opportunities for innovation What We're Looking For • Bachelor's or Master's in Chemistry, Chemical Engineering, Materials Science, or a related scientific discipline, • 3+ years of industrial R&D experience (advanced degrees may substitute for some experience), • Experience in a manufacturing environment, with an understanding of how laboratory formulations translate to commercial production, • Strong background in wet chemistry and formulation development, • Experience working with aqueous systems and organic salts, • Experience developing or optimizing manufacturing and mixing processes, • Strong laboratory documentation and technical writing skills, • Excellent experimental design, data analysis, and problem-solving abilities, • Strong communication and collaboration skills, • Startup or high-growth company experience preferred, • Experience with fire protection chemistry, specialty chemicals, industrial formulations, agricultural chemistry, or related industries is highly desirable What Makes This Role Unique This isn't a role where you'll spend years making incremental changes to a single product. You'll work across multiple formulation challenges, collaborate directly with leadership and manufacturing, and see your ideas move rapidly from the laboratory into commercial production. One week you may be improving formulation stability, the next optimizing a mixing process, developing a new product format, supporting regulatory testing, or troubleshooting a manufacturing issue. If you enjoy variety, ownership, and solving meaningful scientific problems, you'll fit right in. Why You'll Love Working Here • Competitive salary, • Opportunity to help build innovative technology with real-world impact, • High degree of technical ownership and autonomy, • Collaborative, entrepreneurial research environment, • Direct interaction with company leadership and manufacturing, • Opportunity to help shape products from concept through commercialization, • Standard Monday-Friday schedule with no shift work Compensation Expected Salary Range: $95,000-$120,000 annually, depending on education, experience, and technical expertise. Company DescriptionCitrotech is a leader in wildfire protection technology, offering innovative solutions including home defense systems, mobile/ground application units, and fire inhibitor innovations. Our mission is to protect homes, communities, and property from wildfires through cutting-edge products and services.Citrotech is a leader in wildfire protection technology, offering innovative solutions including home defense systems, mobile/ground application units, and fire inhibitor innovations. Our mission is to protect homes, communities, and property from wildfires through cutting-edge products and services.

Job Description Immerse yourself in the vibrant, innovative environment of Tentamus California in Irvine! We're seeking an Analytical Chemist to join our growing Tentamus Team! We're looking for someone who not only embodies boundless enthusiasm for scientific discovery but also thrives on collaboration, creativity, and problem-solving. If you're ready to make a meaningful real-world impact, we can't wait to welcome you aboard! How you will excel as part of our team: The Analytical Chemist will be responsible for conducting qualitative and quantitative chemical analyses on various substances to support research, development, and quality control activities under the direction of the Laboratory General Manager. Main duties include: • Executing established laboratory chemistry procedures to provide accurate and prompt chemistry data to clients., • Perform analytical chemistry testing using various instrumentation such as: GCFID, HPLC, ICPMS, GCMSMS, • Assist, oversee, and mentor Lab Techs to help them advance in their chemistry career., • Reviewing and approving QC data within parameters of precision and accuracy., • Maintaining complete and accurate chemistry documentation of activities in compliance with the Quality System., • Preparing stock standards and reagents as needed, performing dilutions of samples and solutions, weighing stock compounds, preparing standard and fortification solutions, and calibrating preparation of primary analytical methods., • Perform routine maintenance and follow preventative maintenance schedules on various instrumentation., • Notifying chemistry supervisor and taking appropriate actions for non-conformances. Participate in corrective action process., • Ensure the safe and efficient use of laboratory equipment and chemicals. Position Type & Expected Schedule Full-Time | M - F 7AM-4PM / 8AM-5PM | Some weekend/holiday hours required To flourish as an Analytical Chemist, you'll need: Our ideal candidate will be authorized to work in the United States indefinitely without restriction or sponsorship, possess a combination of technical skills, attention to detail, and a strong work ethic. Other qualifications include: • Bachelor's degree in chemistry, biology, or related science field, • 3 –5 years of experience in a commercial lab setting. Experience in testing supplements and nutraceticals is a plus!, • Hands-on experience with analytical techniques such as chromatography, spectroscopy, and wet chemistry methods., • GC and GCMSMS experience highly preferred., • Comfortability with applying tests from USP and FCC monographs, • Proficiency in data analysis software (e.g., ChemStation, Empower) and Microsoft Office Suite., • Strong attention to detail and ability to follow standard operating procedures., • Excellent communication skills, both written and verbal., • Ability to work independently and collaborate effectively in a team environment., • Knowledge of Good Laboratory Practices (GLP) and regulatory requirements is desirable. What's in it for you? Annual Salary between $65,000 - $85,000, comprehensive and low-cost benefit plans (medical, dental, vision, disability, life insurance) Ample PTO and 40 hours of sick time per CA state law, and a matching 401k. Work Environment & Physical Requirements This job operates in an analytical laboratory environment with exposure to chemicals and analytical instrumentation. This role routinely uses standard lab equipment such as beakers, test tubes, flasks, thermometers, and computers, among other instruments. While performing the essential duties of this job, the employee is regularly required to use hands and fingers to hold or feel, reach with hands and arms, talk, and hear. The employee is occasionally required to sit, stand; climb or balance; and stoop, kneel, crouch or crawl. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. About Tentamus: Labs for Life®. We are a global network of full-service accredited analytical laboratories providing crucial quality and safety analysis for clients locally, nationally, and beyond using proven methods of chemistry and microbiology. Many of the products you use and consume daily rely on Tentamus labs. With 20 labs in North America and growing (100 globally), we celebrate having talented diverse scientific and service-oriented professionals. Visit us at Tentamus.com|Follow Tentamus on LinkedIn|Follow Tentamus CA on LinkedIn Job Posted by ApplicantPro

Job Description Laboratory Analytical Chemist Job Responsibilities: The Analytical Chemist will be involved in the application of validated methods in modern analytical techniques, including UHPLC, Triple Quadrupole LC-, GC-MS/MS, ICP-MS, GC-MSD, and qPCR to provide consistently accurate and timely results. The successful candidate will be responsible for maintaining procedures in cGLP and adhering to EH&S guidelines to help assure a high level of laboratory quality control and management systems. The position would further require the continual improvement and development of analytical methods in collaboration with other team members. Laboratory Analytical Chemist Job Duties:  Perform analytical testing of plant samples and plant -derived products within a fast-paced testing laboratory environment.  Generate high-quality data and continually maintain precise laboratory records.  Assure analytical instruments are properly maintained and calibrated according to internal procedures.  Develop and improve analytical techniques, in addition to research and apply new methods to stay current with the testing of the target analytes.  Effectively communicate and present data summaries and laboratory operational needs.  Update and effectively write SOPs.  Independently analyze and troubleshoot problems with analytical instruments and methods.  Maintain an organized and clean laboratory environment and adhere to all internal quality control systems and regulatory compliance guidelines. Qualifications and Educational Requirements:  Experience in the operation of one or more analytical instruments including GC-MS, LCMS/ MS, UHPLC, ICP-MS, and qPCR. Preference given to experience with the ICP-MS.  At least 2-3 years of experience in an analytical chemistry testing laboratory.  Experience in various LIMS and SQL databases.  Ability to manage multiple projects and meet deadlines.  Responsible and conscientious in maintaining QA and QC systems to assure accurate results are reported.  Attention to detail in maintaining laboratory records and analytical procedures.  Ability to work effectively with other team members.  Master’s degree in chemistry, analytical chemistry, biochemistry, material chemistry or other related fields. Company DescriptionPML's mission is to adopt best practices in testing, provide unrivaled customer service and accurate results at an affordable price, be fully compliant with all state and local municipalities, and be on the cutting edge in the industry.PML's mission is to adopt best practices in testing, provide unrivaled customer service and accurate results at an affordable price, be fully compliant with all state and local municipalities, and be on the cutting edge in the industry.

Job DescriptionCompany Description 2nd Shift (12:00 PM - 8:00 PM) Veolia has acquired Clean Earth. As Clean Earth completes its integration into Veolia, recruiting and hiring for this role is being managed in partnership with the Clean Earth talent acquisition team. Veolia in North America is the top-ranked environmental company in the United States for three consecutive years, and the country’s largest private water operator and technology provider as well as hazardous waste and pollution treatment leader. It offers a full spectrum of water, waste, and energy management services, including water and wastewater treatment, commercial and hazardous waste collection and disposal, energy consulting and resource recovery. Veolia helps commercial, industrial, healthcare, higher education and municipality customers throughout North America. Headquartered in Boston, Veolia has more than 10,000 employees working at more than 350 locations across North America. Job Description In this position you’ll be responsible for completing analysis of the waste stream samples per SOPs and waste analysis plan, inventory control for lab reagents, maintenance of the samples/instruments, data entry, analytical equipment usage, associated filing and administrative activities within the laboratory Primary Responsibilities: • Follow permit requirements to collect and test compounds and samples, using applied methods techniques., • Enter quantities, volumes and analytical results into waste management software, • Perform QA/QC analytical screening parameters as dictated by permit. Follow all approved Laboratory SOPs, • Ensure compliance with environmental health and safety standards including the proper handling, storage, and disposal of chemical agents., • Operating and maintain laboratory equipment, • Performs other reasonably related tasks as assigned by management. Starting rate of pay $24.00 per hour Qualifications Basic Qualifications: • Bachelor degree in chemistry or biology, • Ability to work in team and fast paced environment, • Ability to communicate effectively and diplomatically, both verbally and in writing, • Periods of sitting at a desk and working on a computer, • Ability to stand for prolonged periods while conducting lab tests, • Ability to lift 50 pounds throughout the workday, • Ability to complete 40-hour OSHA training with 8-hour refresher courses Preferred Qualifications: • 1+ years Bench experience in analytical chemistry, • Knowledge OSHA Regulations, • 2+ years experience in Hazardous Waste Industry Additional Information Benefits: Comprehensive benefits package includes paid time off policies, as well as health, dental, vision, life insurance, tuition reimbursement, paid volunteering and more. In addition, commencing no later than January 1, 2027, benefits package will include participation in an employer sponsored 401(k) plan, to save for retirement. Pay and benefits for employees represented by a union are outlined in their collective bargaining agreement. We are an Equal Opportunity Employer! All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Disclaimer: The salary, other compensation, and benefits information is accurate as of the date of this posting. The Company reserves the right to modify this information at any time, subject to applicable law.

Job DescriptionProduction Process Chemist (Contract) | Peptide Manufacturing & GMP OperationsOverview We are seeking a Production Process Chemist to provide hands-on technical support for commercial peptide manufacturing operations within a regulated biotechnology environment. This is an excellent opportunity for a chemist or process professional looking to gain extensive exposure to GMP manufacturing, process validation, technology transfer, equipment qualification, and commercial-scale peptide production. In this highly collaborative role, you will partner with Manufacturing, Process Development, Quality Control, and Quality Assurance teams to support production activities, troubleshoot manufacturing challenges, investigate deviations, and ensure compliance with cGMP standards. The ideal candidate is technically strong, detail-oriented, and thrives in a fast-paced manufacturing environment. Key Responsibilities • Provide floor-side technical support for commercial peptide manufacturing operations, including:, • Solid-Phase Peptide Synthesis (SPPS), • Peptide cleavage, • Purification processes, • Lyophilization (freeze drying), • Partner with Manufacturing, Process Development, QA, and QC teams to support routine production and continuous improvement initiatives., • Support technology transfer activities to successfully implement new and optimized manufacturing processes., • Assist with deviation investigations, root cause analysis, and quality system documentation., • Support CAPA (Corrective and Preventive Action) activities through data collection, analysis, and documentation., • Execute and document process validation activities, including:, • Process Performance Qualification (PPQ), • Continued Process Verification (CPV), • Support equipment qualification activities, including:, • Installation Qualification (IQ), • Operational Qualification (OQ), • Performance Qualification (PQ), • Monitor manufacturing processes, analyze production trends, and identify opportunities for process improvements., • Review batch records and manufacturing documentation to ensure accuracy, completeness, and cGMP compliance.Required Qualifications, • Bachelor’s degree in Chemistry, Biochemistry, Chemical Engineering, Bioengineering, or a related scientific discipline., • Experience working in a cGMP-regulated pharmaceutical, biotechnology, or life sciences manufacturing environment., • Knowledge of peptide manufacturing processes, including:, • Solid-Phase Peptide Synthesis (SPPS), • Purification, • Cleavage, • Lyophilization, • Experience supporting process validation activities such as PPQ and CPV., • Experience supporting equipment qualification activities including IQ, OQ, and PQ., • Understanding of deviation investigations, root cause analysis, and quality systems., • Experience supporting CAPA programs and documentation., • Strong technical writing and GMP documentation skills., • Excellent troubleshooting, analytical, and problem-solving abilities., • Strong communication skills and ability to work cross-functionally., • Willingness to spend significant time supporting operations on the manufacturing floor.Preferred Qualifications, • Prior peptide manufacturing experience., • Experience supporting commercial pharmaceutical or biotechnology manufacturing operations., • Familiarity with technology transfer projects., • Experience working within formal quality systems and regulatory environments., • Demonstrated ability to manage multiple priorities in a fast-paced production setting.Work Environment This is a 3-month contract opportunity supporting a leave of absence. The role operates on a Monday–Friday, 8:00 AM–5:00 PM schedule and is heavily focused on manufacturing floor support within a cGMP-regulated production environment. The position offers valuable hands-on exposure to: • Commercial peptide manufacturing, • GMP production operations, • Process validation, • Equipment qualification, • Technology transfer activities, • Quality systems and compliance programsIdeal Candidate This role is ideal for a chemist, process scientist, manufacturing scientist, or process engineer seeking hands-on experience in commercial biotech manufacturing and looking to expand their expertise in peptide production, GMP operations, validation, and technical manufacturing support. Job Type & Location This is a Contract position based out of San Diego, CA. Pay and Benefits The pay range for this position is $28.00 - $33.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in San Diego,CA. Application Deadline This position is anticipated to close on Jul 15, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job DescriptionBenefits: • Life Insurance, • LTD, • Health insurance, • Paid time off, • Vision insurance, • 401(k), • 401(k) matching, • Dental insurance The QC Chemist will be responsible for sampling and testing raw materials, products in mid-production, and finished products. The Chemist will evaluate raw materials that arrive to ensure they meet quality standards and project specifications. Primary duties are to measure and test lab materials and products according to industry-specific standard procedures. We are a contract manufacturer for dietary supplements and sports nutrition products. DUTIES & RESPONSIBILITIES: The following responsibilities would characterize the requirements of this position. Must possess the skills necessary to perform the majority of the listed functions: • Review and approve the documentation setting forth the basis for qualification of any supplier, • Prepare compounds, test solutions, and reagents to conduct tests and experiments, then advising and coordinating on test procedures, • Determine the relationships of chemical and physical properties, composition, and structures, • Develop, improve and customize equipment, products, formulas, analytical methods, and processes, • Document findings in technical papers and reports, preparing specifications, and testing standards, • Clean and maintain laboratory instruments and equipment, • Making sure that all the technology is working correctly, • Conduct quality control tests to ensure no compounds or equipment are contaminated, • Order laboratory supplies and chemicals, keeping an eye on expiration dates, • Follow all company and governmental safety procedures, • Create thorough reports on tests and your findings, • Evaluate testing protocols and suggest improvements REQUIREMENTS: Competencies • Masters degree in Chemistry, Chemical Engineering, Biochemistry, Biomedical or related field is required, • Hands-on experience a must with Inductively Coupled Plasma Mass Spectroscopy (ICPMS). And High-Performance Thin-Layer Chromatography (HPTLC), High-Performance Liquid Chromatography (HPLC) machinery is a plus, • Strong background in Food Science and Chemistry is highly desirable, • Previous experience working in biotechnology, or research laboratory is preferred, • Strong knowledge of analytical chemistry principles, • Proficiency in laboratory techniques, including spectroscopy, chromatography, and wet chemistry methods, • Excellent analytical and problem-solving skills with meticulous attention to detail, • Strong written and verbal communication skills, with the ability to present findings clearly and concisely, • Ability to work both independently and collaboratively in a team-oriented environment, • Familiarity with regulatory guidelines, • Commitment to safety and adherence to laboratory protocols, • Strong organizational skills and the ability to manage multiple tasks and projects simultaneously, • Bilingual Mandarin Preferred

Job Description Solution analysis of process tanks using titration method. Waste Treatment verification. Company DescriptionSpecializing in NDT, Chemical Processing and Paint.Specializing in NDT, Chemical Processing and Paint.

Job Description General Description of Duties The Senior Beverage Scientists analyzes, develops and improves new and existing products utilizing existing and new raw materials. Matches products supplied by customers and internal personnel from competitors. Calculates costing and suggested selling prices on all products developed. Directs the evaluation and testing of prototypes. May provide supervision to and direct the work of all R&D Product Development Chemists as well as Lab Technicians. Essential Job Functions • Must demonstrate superior creativity skills in product development., • Originates and/or develops new and/or existing products including Juice Concentrates and Flavors based on defined customer or in‐house requirements with little to no direction or instructions., • Requires little to no direction or supervision., • Determines feasibility of certain projects based on production capacity, technology, equipment, and any other potential limitations., • Performs cost analysis and suggested selling prices on all work performed., • Creates master formulas and compounding instructions as needed., • Prepares and revises product specification sheets., • Contacts customers technical staff to determine customers' requirements with regard to product development and develops products which meet or exceed customer's needs and application., • Provides technical assistance to customers and brokers., • Provides on-site technical support to customers for 1st time productions and/or any required trouble shooting assistance., • Provides training to all R&D Product Development Chemists., • Organizes and establishes guidelines, procedures, and policies for all outgoing samples., • Assists the Q.C. and Production departments in first time production of all new products., • Assumes responsibility for all sample request inquiries in R&D Product Development Manager’s absence., • Performs other duties and special projects as required., • Must be able to lift 25Lbs. Requirements • Bachelor's degree in Chemistry, Food Science, or a related field., • Minimum of 5 years Chemist experience., • Analytical Skills., • Research and Development (R&D) expertise., • Laboratory Skills., • Strong problem-solving and critical thinking abilities., • Excellent communication and collaboration abilities to work effectively with cross-functional teams., • Supervisory and/or management experience preferred.Company DescriptionAFF manufactures custom juice and flavor blends for a wide variety of industrial users worldwide. Companies come to us for the latest and best ingredient blends and flavor systems for their products. In business over 50 years, we have two manufacturing plants and a distribution warehouse in Southern California. On April 1, 2016, American Fruits and Flavors was acquired by Monster Energy Company which expanded American Fruits and Flavors’ resources, significantly. American Fruits and Flavors, LLC is an equal employment opportunity employer and does not discriminate in hiring or employment upon any basis prohibited by law, including race, color, creed, religion, age, sex, national origin, cancer, genetic characteristics, genetic information, pregnancy, ancestry, sexual orientation, marital status, veteran status, or disability. None of the questions or information sought in this application is intended to discriminate based upon any status protected by law. Compensation Range: Actual salary/hourly wages are determined upon a variety of factors such as level of experience, skills, education and /or certifications, location, and position level AFF manufactures custom juice and flavor blends for a wide variety of industrial users worldwide. Companies come to us for the latest and best ingredient blends and flavor systems for their products. In business over 50 years, we have two manufacturing plants and a distribution warehouse in Southern California. On April 1, 2016, American Fruits and Flavors was acquired by Monster Energy Company which expanded American Fruits and Flavors’ resources, significantly.\r\n \r\nAmerican Fruits and Flavors, LLC is an equal employment opportunity employer and does not discriminate in hiring or employment upon any basis prohibited by law, including race, color, creed, religion, age, sex, national origin, cancer, genetic characteristics, genetic information, pregnancy, ancestry, sexual orientation, marital status, veteran status, or disability. None of the questions or information sought in this application is intended to discriminate based upon any status protected by law.\r\nCompensation Range: Actual salary/hourly wages are determined upon a variety of factors such as level of experience, skills, education and /or certifications, location, and position level

Job Description MAST is seeking a Chemist II to support the development, optimization, scale-up, and production of advanced coatings, elastomers, adhesives, sealants, absorbers, conductive materials, and other polymer-based systems. This role serves as a key technical resource supporting formulation development, manufacturing process stability, customer qualification efforts, and new business growth across the EMI-Fire portfolio. The successful candidate will collaborate closely with Engineering, Operations, Quality, Supply Chain, Sales, Program Management, and customers to develop repeatable material solutions, troubleshoot manufacturing challenges, support qualification programs, and accelerate new product introductions. This position will primarily support MAST Technologies while also providing technical chemistry support to Swift, Spira, and other EMI-Fire businesses as needed. About MAST: MAST, an EMI-Fire business, develops advanced materials and engineered solutions for aerospace, defense, industrial, and emerging technology applications. Our products are designed to perform in demanding environments where material performance, reliability, and manufacturability are critical. Through collaboration across MAST, Swift, Spira, and other EMI-Fire businesses, we deliver innovative solutions that accelerate qualification, production readiness, and mission success. Key Responsibilities Formulation Development & Material Innovation • Develop, modify, and optimize formulations for coatings, elastomers, adhesives, sealants, absorbers, conductive materials, and specialty polymer systems., • Design and execute laboratory experiments and Design of Experiments (DOE) to support product development and process optimization., • Evaluate raw materials, fillers, additives, pigments, conductive agents, and specialty chemistries for performance, manufacturability, and cost improvement opportunities., • Conduct formulation studies to improve material performance, cure behavior, adhesion, durability, environmental resistance, and processability., • Support the transition of products from laboratory development through pilot and production scale-up., • Perform physical, mechanical, thermal, and chemical testing to evaluate product performance., • Analyze test results and prepare technical reports, recommendations, and development documentation., • Coordinate external laboratory testing and qualification activities as required., • Maintain formulation records, technical documentation, and development files to ensure traceability and protect internal technical knowledge. Production Support & Process Stability • Provide technical support to manufacturing operations to improve process consistency, yield, and product quality., • Investigate formulation, material, and processing-related nonconformances., • Lead or support root cause investigations, NCR/MRB activities, CAPA efforts, and corrective actions., • Establish and document manufacturing and application process parameters to improve repeatability and product performance., • Evaluate material variability and its impact on manufacturing consistency and customer requirements., • Drive data-based improvements to reduce scrap, rework, and process variation., • Support validation and implementation of manufacturing process improvements. Customer Qualification & Application Support • Support customer qualification programs through application trials, coupon testing, prototype builds, sample preparation, and validation activities., • Develop technical data packages and supporting documentation for customer evaluations and approvals., • Collaborate directly with customers to understand performance requirements and resolve application challenges., • Provide technical recommendations regarding material selection, processing requirements, and product performance., • Generate repeatable test data and application guidance to accelerate customer qualification timelines. Cross-Functional Business Support • Partner with Sales, Engineering, Program Management, Operations, and Supply Chain during quotation, proposal, development, and commercialization activities., • Assist with material selection and identify development requirements for new business opportunities., • Support Supply Chain in evaluating suppliers, raw materials, and alternative sources based on performance, availability, cost, and risk., • Provide technical input regarding development scope, project risk, and commercialization strategies., • Participate in customer meetings, technical reviews, supplier discussions, and program gate reviews., • Serve as the primary chemistry subject matter expert supporting MAST and other EMI-Fire businesses. Continuous Improvement • Identify opportunities to reduce material costs, improve yields, and optimize manufacturing processes., • Maintain awareness of emerging technologies, materials, and industry trends., • Recommend laboratory equipment, testing capabilities, and capital investments that support business growth., • Support a culture of safety, accountability, continuous improvement, and customer focus., • Perform other duties and projects as assigned. Qualifications Education • Bachelor's degree in Chemistry, Polymer Science, Chemical Engineering, Materials Science, or a related technical discipline required., • Master's degree preferred. Experience • 3–5 years of experience supporting coatings, polymers, elastomers, adhesives, sealants, composites, absorbers, or specialty materials. Preferred Experience • Formulation development of coatings, elastomers, adhesives, sealants, absorbers, or specialty polymer systems., • Aerospace, defense, industrial manufacturing, or advanced materials environments., • Manufacturing scale-up, process optimization, and troubleshooting., • Customer qualification programs, application trials, and validation activities., • Design of Experiments (DOE) and statistical analysis methods. Skills • Strong understanding of polymer chemistry and formulation science., • Knowledge of coating technologies, rheology, curing mechanisms, and material processing., • Hands-on laboratory and manufacturing experience., • Strong analytical, troubleshooting, and problem-solving abilities., • Ability to interpret technical data and develop practical solutions., • Effective written, verbal, and interpersonal communication skills., • Proficiency with Microsoft Office applications., • Experience with laboratory testing equipment and analytical techniques., • Strong organizational skills and attention to detail., • Ability to manage multiple priorities in a fast-paced environment., • Ability to obtain and maintain a U.S. security clearance preferred. Benefits: At MAST, we recognize how important your career and benefits are to you and your family. We offer a full suite of benefits, including medical, dental, vision, short and long-term disability coverage, accident insurance, critical illness insurance, basic and supplemental life insurance, employee assistance plan, retirement savings and matching, and other developmental opportunities. We are committed to supporting the way you live and work. MAST is an Equal Opportunity Employer. We consider all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other legally protected status. Applicants requiring reasonable accommodation to complete the application process may contact Human Resources. This position requires access to information subject to the International Traffic in Arms Regulations (ITAR). Employment is contingent upon the applicant being a “U.S. person” as defined by ITAR (22 CFR §120.15), which includes U.S. citizens, lawful permanent residents, refugees, or asylees, as required by U.S. export control laws.

Job DescriptionBioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a Chemical Operator/Mixer to work for a Greater Los Angeles area pharmaceutical company. Pay Rate: $20-25/hour depending on experience. Responsibilities: • The operator is required to perform batching operations under the supervision of a chemist., • Duties include complete setup of mixing and processing equipment, weighing of ingredients, compounding, chemical stock handling, equipment and area cleanup, and light equipment maintenance (lubrication, minor adjustments, etc.)., • Completing production forms is critical and performing all operations in a consistent manor is required. Fork lift operation is also required., • The areas of training include:, • Weighing operations in metrics, • Basic materials handling, • Basic mixing and blending operations, • Safety in operations and material handling, • Equipment care, use and storageQualifications:, • U.S. High School Diploma minimum (must be able to demonstrate general knowledge and skills by passing the standardized company test), • Proficiency in the English language and communication skills mandatory for following written setup instructions and completing production forms required by FDA and IS0 regulations, in addition to safety considerations in a chemical manufacturing facility., • 2-3+ years in a manufacturing environment and compounding industrial size formulations., • Excellent mathematical skills are required for counting, weighing, materials calculation, and execution of written compounding instructions., • In addition, good mechanical aptitude is necessary to perform occasional trouble-shooting, setups, and completing routine maintenance on compounding equipment.Please send resumes to tiffany@biophaseinc.com and visit our website at www.biophaseinc.com for additional job opportunities!!!

Job DescriptionCompany Description Veolia has acquired Clean Earth. As Clean Earth completes its integration into Veolia, recruiting and hiring for this role is being managed in partnership with the Clean Earth talent acquisition team. Veolia in North America is the top-ranked environmental company in the United States for three consecutive years, and the country’s largest private water operator and technology provider as well as hazardous waste and pollution treatment leader. It offers a full spectrum of water, waste, and energy management services, including water and wastewater treatment, commercial and hazardous waste collection and disposal, energy consulting and resource recovery. Veolia helps commercial, industrial, healthcare, higher education and municipality customers throughout North America. Headquartered in Boston, Veolia has more than 10,000 employees working at more than 350 locations across North America. Job Description PRINCIPAL DUTIES AND RESPONSIBILITIES: • Handles hazardous materials including inventorying, identifying, segregating, and packaging waste material in accordance with Lab Pack policies, procedures and practices and all applicable regulations., • Perform onsite services which may include waste collection, consolidation (i.e., bulking, repackaging), sampling, safety/compliance inspections, and other related activities required by the customer/contract., • Assists other business groups, i.e., Depack, Retail and HHW, for both internally and onsite as needed. • Preparing shipment of packaged waste by inspecting, labeling, marking, and loading into the transport vehicle, • Properly completes documentation including shipping papers, Land Disposal Restrictions (LDR’s), evaluations/certifications and other required documentation in accordance with appropriate regulations and procedures., • May require obtaining and maintaining a Commercial Driver’s License (CDL) with Hazmat Endorsement to legally operate Clean Earth vehicles necessary for transporting personnel and waste to and from customers’ job locations., • Follows, understands, and promotes by example, all Health & Safety /Job Safety Analysis (JSA’s) procedures including development of on-site Health &Safety plans/JSA’s as outlined in the procedures and policies., • Performs other duties as assigned. Pay range $30.00 - $30.00 Qualifications Basic Requirements: • An associate’s degree in general science (BS preferred) is required for the Lab Pack Chemist., • Driver’s License with clear record, • Moderate to extensive travel with 2% overnight travel, • Physical ability to lift and move material of various weights frequently exceeding 55 lbs., • Basic understanding of chemistry through general chemistry or biology This position requires a CDL B to be obtained within a 6-month period from your start date. Selected candidates will receive paid training during standard working hours, with Veolia covering the cost of the program. Failure to obtain a CDL B within the 6-month period will mean you are no longer eligible for the Lab Pack Chemist position. This position is also contingent upon successful completion of a DOT physical, DOT Drug Screen and any other DOL or company requirements. Must be willing to travel and Layover when the job requires it. Additional Information Benefits: Comprehensive benefits package includes paid time off policies, as well as health, dental, vision, life insurance, tuition reimbursement, paid volunteering and more. In addition, commencing no later than January 1, 2027, benefits package will include participation in an employer sponsored 401(k) plan, to save for retirement. Pay and benefits for employees represented by a union are outlined in their collective bargaining agreement. We are an Equal Opportunity Employer! All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Disclaimer: The salary, other compensation, and benefits information is accurate as of the date of this posting. The Company reserves the right to modify this information at any time, subject to applicable law

Job DescriptionAmerica is critically deficient in production of defensive munitions- we currently produce shipborne interceptors in the few hundreds per year while our adversaries are producing offensive threats in the tens of thousands per year. Furientis was started to help solve this problem- introducing a new class of cost-effective, high production rate, interceptor missiles. We're seeking motivated individuals who internalize this problem and are eager to apply their past experience in similar industries (aerospace, defense, automotive/racing, robotics) and out of the box thinking to solve this problem for the US and its allies.About the Team The Propulsion Team designs, builds, and flies the solid rocket motors that power our interceptor. We own the chemistry, the motor and grain design, the ground test campaigns, and the range operations. About the Role We are looking for a chemist or chemical engineer who will own our composite propellant: formulation, mix and cure process, ingredient sourcing, and characterization. You will report to the Head of Propulsion. This is a hands-on role for someone who has already taken a composite propellant from formulation through motor flight or qualification, and who prefers cheap, well-understood chemistry to high-energy energetics or one-source materials. Every formulation choice is also a unit-cost choice, and we expect you to design accordingly. What You'll Do • Own propellant formulation: composition tradeoffs, ingredient selection, and the cost-vs-performance calls that go with both., • Develop the mix and cure process: vacuum mix profile, ingredient addition order, cure schedule, pot life., • Source and technically qualify ingredients across the propellant supplier base. The Head of Supply Chain owns commercial terms., • Characterize each formulation: burn rate at temperature, pressure exponent, density, mechanical properties, strain-to-failure, aging., • Match propellant properties to motor architecture with the development engineer., • Design the dual-pulse chemistry: pulse-1 and pulse-2 composition selection, mechanical and thermal compatibility, interpulse barrier interaction., • Write the mix SOPs and qualification documentation., • Own the chemistry side of facility safety and compliance: storage planning, hazardous-materials handling, ATF and AHJ documentation.Skills We're Hiring For, • B.S. or M.S. in Chemistry, Chemical Engineering, Materials Science, or related., • 5+ years hands-on composite-propellant formulation and mix process development. At least one propellant where you carried it from formulation through motor flight or qualification., • Fluency with HTPB, AP, aluminum, curative, plasticizer, and bonding agent chemistry: ingredient interactions, cure mechanisms, mechanical property tradeoffs., • Hands-on mix experience: vertical and planetary mixers, vacuum mixing, cast and cure cycle development., • Working fluency with thermochemistry codes for predicting Isp, flame temperature, c*, and product species across a composition range., • Hands-on burn rate measurement: strand burner, pressure exponent, temperature sensitivity., • Mechanical property testing of cured propellant: uniaxial tensile, modulus, strain-to-failure across operating temperature., • Real working network of composite-propellant ingredient suppliers across AP, HTPB, aluminum, and curative families., • A real track record of meeting motor performance without reaching for exotic chemistry or one-source materials. No high-energy oxidizers, no nano-aluminum, no exotic binders., • AI-native working style: daily use of agentic coding tools (Claude Code, Codex, OpenCode, or similar) for formulation tradeoff scripting, thermochemistry runs, and characterization data reduction.Bonus Points For, • Direct dual-pulse propellant development., • Aging and shelf-life qualification experience., • Stood up a propellant mix facility from scratch., • ATF, OSHA PSM, and EPA compliance experience for energetic-materials operations., • Burn rate modifier and ballistic modifier formulation work., • Out-of-domain chemistry background that gives you practical, first-principles intuition (polymer chemistry, battery formulation, hazardous-process work). We actively want people who can solve propellant problems without dragging legacy-prime habits with them. Eligibility & Logistics Location: On-site at our Los Angeles, CA HQ; remote work is not available. Monthly weekend travel for test events and supplier engagements. Clearance: A clearance is not required for this position. Must be a U.S. Person. Equal Opportunity & Export Compliance Furientis is an equal-opportunity employer. To comply with U.S. export control laws, employment is contingent on eligibility to access export-controlled information. AI assists in reviewing applications. Humans make final hiring decisions. Contact us with questions.

Job Description Immediate opening for MS/PhD Organic Chemist to support custom synthesis group. The ideal candidate will possess experience in small-scale organic synthesis with knowledge of practical and modern synthesis methodology, as well as chromatographic methods such as HPLC, TLC and GC. Experience with radiometric analysis and vacuum line techniques a plus. We offer a competitive salary, bonus program, health and dental benefits, flex-time and a relaxed working environment.

Job DescriptionQC Analytical Chemist I - Torrance, California Rate: $26.00 to $29.00 ●Analyzes raw material compounds, bulk and finished goods to determine chemical and physical properties. ●Complete routine review of QC test data and related documents for in-process samples, finished goods and stability samples. ●Follows established procedures and documents all findings and results timely, concisely, clearly and accurately. ●Prepares standards and specifications for processes, facilities, products, and tests. ●Provide updates/escalations at daily and weekly site-specific and cross-site meetings. ●Aids in root cause analyses and corrective/preventive action (CAPA) initiatives related to quality issues, including product Out-of-Specifications, deviations and consumer complaints. ●Aids in improvements of the stability program, including initiating stability protocols, stability inventory schedules, stability pulls, ensuring timely testing of products, compiling stability reports, and trending data across the shelf-life of OTC products. ●Collaborate with cross-functional teams to support continuous improvement initiatives. ●Assists in the development, review, writing, and implementation of SOP's for quality functions to ensure compliance with all regulatory and GMP requirements. ●Experience with method development/qualification, tech transfer, QC testing, and laboratory deviations/investigations ●Experience with analytical testing methods (organoleptic, viscosity, pH, moisture, specific gravity, titration assays, FTIR) in cosmetic and OTC manufacturing environment to support QC testing, data reviews, & COA generation to support testing and release. ●Assessment of GMP systems currently in place to ensure compliance and provides solutions to improve quality systems. ●Proficiency in MS Word, Excel, Power Point and other applications ●Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment ●Works with development of formulas, processes, and methods for solution of technical problems. ●Strives toward continuous self-improvement in personal productivity. ●Comfortable in a fast-paced environment with minimal direction and able to adjust workload and flexibility based upon changing priorities ●May aid in monitoring and trending raw material, in-process, finished goods and stability data results Preferred: ●Demonstrated self-management skills, including establishing direction and goals, and building good work ethics for the team ●Experience with microbiological testing methods. Qualifications: ●Minimum 3 years of experience in a QC Laboratory or regulated manufacturing environment preferred (cosmetics or OTC drugs a plus). ●Bachelor’s degree in a scientific or technical field (e.g., Chemistry, Biology, Pharmaceutical Sciences). ●Working knowledge and understanding of GMP, FDA regulations and quality systems, and regulatory requirements (21 CRF Part 11/ 210/ 211). ●Knowledge of regulatory guidance and experience maintaining QC lab GMP compliance and audits ●Strong attention to detail and organizational skills. ●Effective written and verbal communication skills. ●Proficiency in Microsoft Office and familiarity with electronic quality systems is a plus. ●Maintains an exemplary attendance and punctuality performance record. ●Adheres to all Prime Personnel Policies as established by the company. What we are offering: ●Competitive compensation package. ●Health, dental, and vision benefits. ●401K program. ●The spirit of a startup with the security of an established, profitable industry leader. ●The opportunity to make waves in a $250B industry. Powered by JazzHR 07Xn9xkENM

Job Description Seeking self motivated experienced medicinal chemist to help lead custom synthesis group. Primary job responsibility involves development of key radiolabeled starting materials and their application into the synthesis of complex drug structures. Familiarity with vacuum line techniques, small scale isotope synthesis, HPLC and radiometric analyses will support the ideal candidate. Proven record of hands on experience with a wide variety of organic synthesis transformations required. Superior communication and documentation skills desired.

Job Description Based in the Los Angeles/Carson corporate headquarters, Dermalogica is seeking an Associate Chemist to support R&D formulation development. This hands-on laboratory role supports Formulating Chemists and Senior Chemists by preparing bench batches, executing experiments with scientific discipline, documenting results, and supporting samples for development, stability, compatibility, and cross-functional needs. Essential Duties and Responsibilities: 1. Bench Formulation and Sample Preparation • Prepare lab-scale batches under direction, including weighing raw materials, mixing, heating/cooling, pH adjustment, homogenization, filling, and sample labeling., • Support prototypes, formula iterations, marketing submissions, benchmark comparisons, panel samples, stability/compatibility fills, clinical/education samples, and other R&D sample requests., • Maintain accurate lab notes, batch records, sample labels, retains, and sample inventory with strong attention to detail. 1. Experimental Execution and Formulation Support • Execute designed experiments, raw material screens, reformulation support batches, and prototype adjustments according to direction from the project owner., • Record key observations and data such as appearance, odor, color, texture, pH, viscosity, weight, temperature, mixing speed, processing time, and equipment used., • Compare samples against controls, benchmarks, and prior versions; communicate observations clearly and escalate unusual results or processing concerns promptly., • Assist with support batches and documentation for stability, package compatibility, preservative efficacy testing, safety/clinical testing, formula quotes, and regulatory review packages. 1. Laboratory Operations, Safety, and Good Documentation • Work comfortably in the lab and perform the practical hands-on aspects of bench formulation, including standing at the bench, handling lab-scale containers, operating routine equipment with training, and cleaning/organizing work areas., • Follow laboratory safety procedures, PPE requirements, chemical hygiene practices, SOPs, and GLP/GMP-aware documentation expectations when handling cosmetic raw materials, fragrances, essential oils, and lab chemicals., • Use routine lab equipment such as balances, pH meters, viscometers, hot plates, overhead mixers, homogenizers, water baths, and filling tools with proper training and care., • Update project/sample tracking systems such as Coptis/Ithos, Wrike, or other R&D systems as needed, while protecting confidential formula, supplier, and project information. Qualifications: • Bachelor's degree (BS) in Chemistry, Cosmetic Science, Biology, Pharmaceutical Science, Chemical Engineering, or a related scientific field., • 0 to 3 years of relevant laboratory or formulation experience; internship, co-op, academic lab, cosmetic/personal care, pharmaceutical, food, or related product development experience will be considered., • Comfortable spending adequate time in a laboratory environment performing practical bench work with accuracy, patience, and scientific discipline, including standing, handling lab-scale containers, and using standard laboratory equipment with or without reasonable accommodation., • Strong attention to detail, accurate documentation habits, and ability to follow written procedures and verbal instructions., • Basic understanding of laboratory safety, PPE, chemical handling, GLP/GMP principles, and good documentation practices., • Excellent written and verbal communication skills with the ability to collaborate in a team-oriented, fast-paced R&D environment., • Proficiency with Microsoft Office is a must. Familiarity with formulation systems, project management tools, or laboratory data systems is a plus. Preferred Experience: • Prior experience in cosmetics, personal care, pharmaceutical, food, or related formulation laboratory work is preferred., • Exposure to emulsions, surfactant systems, gels, serums, sunscreen/SPF systems, stability testing, or package compatibility testing., • Experience using pH meters, viscometers, balances, overhead mixers, homogenizers, hot plates, or similar lab equipment., • Basic ability to organize data, summarize observations, and communicate experimental results clearly. This position will be based out of the corporate headquarters in Carson, CA with full on-site office work guidelines. The base salary for this position is $70.5K. The role is eligible for participation in our company bonus plan, rewarding personal performance and company results. If you are ready to contribute to Dermalogica's mission, we would love to hear from you! To be considered for this role, please complete your online application. A member of the Human Resources team will contact you if your experience and skills are a match for the position. Dermalogica is an equal opportunity employer committed to fostering an inclusive culture where all employees are valued, supported, and empowered to succeed.

Job Description Production Process Chemist - Simply Biotech OVERVIEW Are you looking for a new career opportunity with an exciting biotech company?! Then we have got the right team for you! In this role, you are responsible for the duties listed below. Immediate opening for a Production Process Chemist in San Diego, CA who possesses: • Bachelor's degree in Chemistry, Biochemistry, or a related science field, • Strong organizational skills and attention to detail, • cGMP, peptide manufacturing, or batch support experience is a plus FULL DESCRIPTION: We are seeking a Production Process Chemist to support peptide manufacturing processes from technology transfer through commercial production. This 3-month temporary role will provide floor-side technical support, assist with investigations and troubleshooting, support equipment qualification, and contribute to process documentation, PPQ, and CPV activities. The ideal candidate will have a science background, strong organizational skills, and an interest in learning manufacturing processes, cGMP documentation, and batch support within a peptide manufacturing environment. The selected candidate will be responsible for: • Providing floor-side technical support during peptide manufacturing operations, including SPPS, cleavage, purification, and lyophilization, • Assisting with investigations and troubleshooting of critical manufacturing issues, • Collecting data and performing technical assessments, • Supporting deviation investigations, root cause analysis, and CAPA implementation, • Supporting technology transfers between Process Development and Manufacturing, as well as across manufacturing sites, • Helping ensure strong process understanding, reproducibility, and complete GMP documentation during transfer and production activities, • Assisting with Process Performance Qualification activities, including protocol execution support, data collection, data review, and reporting, • Supporting Continued Process Verification through process monitoring, trend analysis, and identification of potential process variability, • Supporting qualification of new manufacturing equipment, including IQ, OQ, and PQ protocol execution, • Preparing and maintaining related GMP documentation, • Helping improve manufacturing workflows and batch documentation to reduce human error, strengthen data integrity, and improve operational consistency, • Collaborating cross-functionally with Manufacturing, Process Development, Quality Control, and Quality Assurance, • Supporting routine operations, investigations, and new production introductions, • Learning and supporting peptide manufacturing processes, paperwork, and batch-related documentation as needed The selected candidate will also possess: • Bachelor's degree in Chemistry, Biochemistry, or a related field required, • Minimum of 1 year of experience in pharmaceutical manufacturing or a cGMP environment preferred, • Peptide manufacturing experience preferred, • Foundational understanding of cGMP manufacturing principles, • Familiarity with peptide manufacturing processes, including SPPS, cleavage, purification, and lyophilization preferred, • Familiarity with equipment qualification, including IQ, OQ, and PQ preferred, • Hands-on exposure to process validation activities, including PPQ execution and CPV support, preferred, • Understanding of cleaning validation principles, residue risk assessment, and contamination control preferred, • Familiarity with quality systems, including deviations, investigations, CAPAs, and change controls, • Strong verbal and written communication skills, • Ability to communicate technical information clearly to operators, peers, and cross-functional partners, • Hands-on, proactive mindset with willingness to work directly on the manufacturing floor, • Developing problem-solving and troubleshooting skills, • Ability to collaborate effectively across Manufacturing, Process Development, Quality Control, and Quality Assurance, • Strong attention to detail and commitment to compliance, data integrity, and operational excellence, • Ability to balance process robustness, compliance, and manufacturing efficiency, • Ability to work onsite in San Diego, CA, • Ability to work a temporary 3-month assignment, • Ability to work Monday through Friday, 8:00 AM to 5:00 PM or 7:30 AM to 4:30 PM Physical Requirements: • Ability to sit, stand, and walk throughout the workday, including time on the manufacturing floor, • Ability to use hands and fingers for documentation, computer work, data entry, and handling materials or equipment as needed, • Ability to review batch records, GMP documentation, technical data, reports, and computer screens for extended periods, • Ability to communicate by phone, email, video meeting, and in person throughout the workday, • Ability to occasionally bend, reach, lift, carry, or move standard laboratory, manufacturing, or office materials as needed, • Ability to work in a cGMP manufacturing environment while following applicable safety, gowning, documentation, and quality procedures, • Ability to wear required personal protective equipment as needed for manufacturing or production floor support Salary Range: $28 to $30/hour More information can be found at www.simplybiotech.com. Company DescriptionSimply Biotech was founded in 2008 and has been repeatedly recognized as one of San Diego County's fastest growing businesses. In 2025, we were named Business Journal's 'Best Places to Work'. Even as our competitors are scaling back and laying off staff, Simply Biotech is expanding to new markets and hiring additional staff in existing offices.Simply Biotech was founded in 2008 and has been repeatedly recognized as one of San Diego County's fastest growing businesses. In 2025, we were named Business Journal's 'Best Places to Work'. Even as our competitors are scaling back and laying off staff, Simply Biotech is expanding to new markets and hiring additional staff in existing offices.

Job Description Beloteca, Inc. is a generic pharmaceutical development company specializing in the development of injectable products. It is desirable that the candidate have past practical experience and education in handling chemicals, operating laboratory equipment, generating and manipulating data, as well as computer database and word-processing skills. Job Description: • Independent execution of various standard laboratory techniques, including but not limited to H/UPLC, GC, water content analysis per USP, appearance assessment, water activity per USP, • May participate in qualification/verification of assays, • Assay and documentation review and report writing, • Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices., • Execution of more advanced analytical techniques with assistance such as LC/MS, DSC, and TGA, • Independent preparation of samples, solutions, instrument set-up and breakdown, • Independent preparation of data packets and creation of stability data sheets and Certificates of Analysis to summarize analytical testing, • Assisted participation in Out of Specification investigations and the documentation of analytical deviations along with Qualified Investigators and management, • Understand and apply ICH and FDA guidance Basic Qualifications: • BS in Biology, Chemistry and/or related science discipline., • Computer literacy in Windows applications and the MS Office., • Excellent oral and written communication skills are essential., • Minimum of 3 years experience with HPLC, UPLC, GC, Karl Fisher, pH, • Maintain a safe working environment for all employees, ensuring compliance to all local, state, and federal codes and regulations. Preferred Qualifications: • Ability and willingness to work flexible hours., • Great attention to detail, quality, and a desire for success., • Self-motivated individual with the ability to learn, lead and strengthen the Beloteca, Inc. team.

Job Description Job Title: R&D Chemist (Chemist II or Chemist III) Job Description This role offers the opportunity to join a small, collaborative research and development team as an R&D Chemist at either the Chemist II or Chemist III level. You will focus primarily on finished product stability studies and routine analytical testing for nutraceutical and pharmaceutical solid dosage forms. Working closely with another chemist and the broader R&D group, you will perform HPLC assays, support method development, coordinate work with external laboratories, and help maintain an efficient, well-organized laboratory environment. Responsibilities • Conduct finished product stability studies as the primary responsibility, including planning, execution, and documentation of stability interval testing., • Perform routine analytical testing using small molecule HPLC, working primarily with Shimadzu HPLC instrumentation., • Carry out solid dosage testing such as disintegration, weight discrepancy, and other physical tests on nutraceutical products., • Prepare, organize, and submit samples and associated paperwork to external contract laboratories., • Enter analytical data and stability results into LIMS and other electronic software systems, ensuring accuracy and completeness., • Support method development and validation activities under the guidance of staff, contributing to system improvements and method optimization., • Assist with small-scale stability studies and occasional bench-scale formulation work under direct supervision., • Order laboratory reagents, consumables, and supplies, and manage purchasing needs for upcoming weeks and months., • Coordinate the shipment of equipment for calibration and maintain records related to instrument maintenance., • Handle hazardous waste in accordance with applicable requirements and assist with hazardous waste disposal procedures., • Maintain general lab cleanliness and organization, including routine cleaning tasks and upkeep of work areas., • Complete detailed, fully electronic documentation for stability study interval testing and other laboratory activities; no paper lab notebooks are used., • Contribute to product development and other non-routine tasks based on experience level and demonstrated capability., • For Chemist III level: oversee lab ordering, manage sending samples to contract labs, coordinate stability interval tools, and take on more administrative and coordination responsibilities within the lab., • Collaborate closely with the full-time and part-time chemists and the R&D team to ensure testing timelines and project goals are met., • Plan ahead to anticipate laboratory needs, manage multiple tasks, and maintain consistent productivity during routine and non-routine work. Essential Skills • Bachelor’s degree in Chemistry or a closely related scientific discipline (minimum requirement)., • Approximately 5–10 years of experience as a chemist in a laboratory environment, which may include quality control or R&D roles in nutraceutical or pharmaceutical settings., • Hands-on experience performing HPLC assay testing in a laboratory environment, preferably in an R&D setting; quality control lab experience is also acceptable., • Proficiency with Shimadzu HPLC instrumentation or similar HPLC systems., • Strong experience in analytical chemistry, including small molecule analysis and wet chemistry techniques., • Experience working with solid dosage forms and related physical testing (e.g., disintegration, weight discrepancy)., • Familiarity with nutraceutical and/or pharmaceutical product testing and quality expectations., • Ability to follow Good Manufacturing Practice (GMP) or similar quality systems in a laboratory environment., • Demonstrated experience with data entry and documentation in electronic systems, such as LIMS or other laboratory software., • Ability to handle hazardous waste safely and in compliance with applicable requirements., • Strong organizational skills with the ability to plan ahead, manage multiple tasks, and maintain a high level of consistency and efficiency., • Ability to work independently, use time effectively, and maintain focus on both routine and non-routine tasks., • For Chemist II: approximately 5 years of experience with HPLC assay testing and physical testing in a lab environment., • For Chemist III: approximately 5–10 years of experience, including responsibility for lab ordering, coordination with contract labs, and administrative support of stability programs. Additional Skills & Qualifications • Experience with finished product testing is a significant plus, particularly for nutraceutical or pharmaceutical products., • Experience working with botanicals is a strong plus., • Exposure to product development activities and non-routine R&D tasks., • Comfort working in a fully electronic documentation environment without traditional lab notebooks., • Ability to support method development and validation under supervision and contribute ideas for system improvements., • Strong communication skills to collaborate effectively with a small R&D team., • Eligibility for medical, dental, and vision benefits, as well as 401(k) participation through the consulting organization., • Access to a variety of partner perks, including discounts on cell phones, consumer goods, and other services through corporate partners., • Eligibility for 24 hours of California sick pay after 90 days of employment, subject to applicable policies., • Eligibility for paid time off, including 40 hours of PTO, subject to applicable policies and employment terms. Work Environment This position is fully onsite at a laboratory facility in Mission Viejo. You will work in a small, close-knit environment with approximately 12 people onsite, including one full-time chemist, one part-time chemist, and the R&D leadership team. The lab uses Shimadzu HPLC systems and supports stability studies, physical testing, and small-scale formulation work primarily on finished nutraceutical and pharmaceutical products. The culture emphasizes organization, independence, and efficient use of time; chemists are expected to plan ahead for the coming weeks, manage their workload proactively, and maintain a well-organized lab. The schedule is Monday through Friday, 8:00 a.m. to 4:30 p.m. The work involves routine bench testing, electronic documentation, coordination with external contract labs, and occasional administrative tasks related to ordering and equipment calibration. Dress is typical for a laboratory environment, with appropriate lab attire and personal protective equipment required while performing testing and handling chemicals. Job Type & Location This is a Contract to Hire position based out of Mission Viejo, CA. Pay and Benefits The pay range for this position is $30.00 - $40.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Mission Viejo,CA. Application Deadline This position is anticipated to close on Jul 24, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job DescriptionBenefits: • Life Insurance, • LTD, • Health insurance, • Paid time off, • Vision insurance, • 401(k), • 401(k) matching, • Dental insurance The Research and Development Formulation Chemist performs various project duties supporting the product development of a contract manufacture of Nutraceuticals and Dietary Supplements. This includes FPS process, formulation, bill of materials database maintenance, and record retention SOPs and new product process. DUTIES & RESPONSIBILITIES: The following responsibilities would characterize the requirements of this position. Must possess the skills necessary to perform the majority of the listed functions: 1. Interpret customers explanations, descriptions and requests and convert them to the chemical components and formula combinations, 2. Meet with suppliers and technical experts for product information collecting newest developments and formulating appropriate applications., 3. Assemble chemicals and materials into laboratory batches and test formula for efficacy/performance, 4. Modify, substitute, and reformulate materials to meet highest level of customer expectations, and quality while maintaining lowest formulation costs, 5. Evaluate alternate chemical suppliers, 6. Enter and review formulas in computer system, 7. Trouble shoot formula issues related to manufacturing/compounding, 8. Revise priorities keeping all deadlines under control according to production demands, customer needs and company interests., 9. Maintain professional expertise through individual study, continuing education and professional development, 10. Must communicate progress, problems and needs with management, vendors, customers as appropriate, 11. Assist with managing the product development process from the concept phase to the post-launch analysis phase, 12. Involvement in new product concept brainstorming meetings, 13. Primary liaison with overseas vendors for Product Development from artwork to product specifications, sculpting, and sample approval, 14. Negotiate pricing with oversees vendors, 15. Set up item number and other development information in item master while updating and maintaining it, 16. Ensure the accuracy of product and packaging samples and seek approvals, 17. Guarantees deadlines are met to obtain samples for tradeshows & licensor, 18. Initiates collateral requests within the Creative Department and/or with outside service vendors, 19. Works with Quality Compliance department regarding compliance issues REQUIREMENTS: Competencies 1. M.S or B.S. degree in Chemistry, Biology, Food Science or other physical science, 2. 2-3 years experience in formulation of new and innovative personal care products, preferably in a contract manufacturing environment, 3. Ability to multitask handling 4-5 bench projects at a time, 4. Ability to thrive within a team environment, 5. Working knowledge of claim substantiation, 6. Current knowledge of ingredient technology and familiar with working within customer and international, 7. Extensive knowledge of laboratory procedures, test instrumentation, and experimental design, 8. Advance writing, reading, and math skills including statistical analysis, 9. Ability to interpret, analyze, reason, and plan

Job DescriptionJob Description Sr. Chemist or Product Development Manager About the Company: Propedix is a biopharma and consumer health company dedicated to advancing innovative treatments in healthcare. Our flagship product Dryello for Athletes Foot, featuring our breakthrough anti-fungal and drying agent technology, launched in Q3 2025, and we have a pipeline of advanced OTC and Rx treatments in dermatology and health. Driven by strong research and development, were delivering the next generation of topical skin solutions. Position: Sr. Chemist or Product Development Manager (30 hours per week for contract or Full time for W-2 Postion ) Position Overview: The Chemist or Product Development Manager will play a key role in the research, development, testing, and commercialization of new OTC dermatology and anti-fungal products, with an initial focus on next-generation anti-fungal sticks and related topical technologies. This position combines hands-on scientific work with project management responsibilities and coordination with contract manufacturers, testing laboratories, and development partners. The position will work closely with the Director of Manufacturing, Project Manager, Chief Medical Officer, and Chair of the SAB. Chemist, Product Development Manager Responsibilities A. Product Development & Formulation Support Support development of new anti-fungal and topical OTC products. Manage formulation development, prototype evaluation, and product optimization. Coordinate laboratory testing and stability studies of products in development. Maintain accurate experimental records and technical documentation. B. Chemical Analysis & Testing Conduct and oversee chemical and physical testing of raw materials and finished products. Review analytical data generated by third-party laboratories. Assist in development and validation of analytical methods. C. New Product - Project Management Work with Companys project manager to ensure product development projects are properly documented, evaluated, tracked from concept through commercialization. Coordinate activities among CMOs, testing laboratories, and internal stakeholders. Investigate product quality issues and support root-cause analyses. D. External Partner Management Serve as a primary technical contact for CMOs and external laboratories. Coordinate sample submissions, testing schedules, and technical communications. Location: Remote position with requirement to be in the lab at least 2 days per week (on average) and attend in-person all day meetings on a monthly basis. Due to the in-person lab requirements, candidates should reside in either a) Northern Colorado (DenverFort Collins corridor) or b) Southern California (Orange County or San Diego County). Education/ Experience/ Necessary Skills Education: Bachelors degree required in Chemistry, Biochemistry, Chemical Engineering, Industrial Engineering, Physics, or a related STEM discipline. Advanced technical degree highly advantageous but not required. Experience Requirements: Senior Chemist: 5 to 10 years of relevant industry experience. Product Development Manager: 7 to 12 years of relevant industry experience including experience leading and managing new formulations development processes through the clinical development. Very strong preference in either position for experience in OTC pharmaceuticals, dermatology, topical products, cosmetics, consumer health products, or regulated manufacturing environments. Candidates without OTC, biopharma industry, consumer health/cosmetics and lab experience should not apply. Knowledge and familiarity FDA processes required. Skills & Competencies: Analytical & Instrumentation Skills • Proficient in operating and maintaining analytical instrumentation, including HPLC, GC, FTIR, UVVis, Karl Fischer, viscometers, pH meters, analytical balances, and titration systems., • Skilled in method execution, sample preparation, calibration, and troubleshooting of routine analytical equipment., • Ability to perform quantitative and qualitative analysis of raw materials, inprocess samples, and finished formulations., • Experience interpreting chromatograms, spectra, and other analytical outputs to support formulation decisions and quality investigations., • Familiarity with stability testing, degradation profiling, and analytical method verification.Formulation Development & Product Creation, • Handson experience compounding, batching, and preparing prototype formulations for topical, dermal, or personalcare products., • Ability to design and execute benchscale experiments, adjust formulation variables, and document results with scientific rigor., • Skilled in evaluating physical and chemical properties (viscosity, hardness, spreadability, homogeneity, phase stability, pH, density)., • Experience scaling formulations from bench to pilot and supporting tech transfer to manufacturing., • Understanding of ingredient functionality (emollients, emulsifiers, actives, preservatives, humectants, rheology modifiers) and how they influence product performance.Testing, Characterization & Quality, • Ability to perform routine QC tests, including (but not limited to) appearance, viscosity, pH, specific gravity and melting point., • Experience conducting accelerated and realtime stability studies, including sample pulls, data trending, and reporting., • Skilled in rootcause analysis, deviation support, and contributing to CAPA investigations., • Familiarity with raw material qualification, COA review, and supplier documentation.Regulatory, GLP, and GMP Compliance, • Working knowledge of relevant Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) for documentation, data integrity, and sample handling in a CPG or OTC environment, including batch record review, change control, and controlled documentation., • Ability to follow SOPs, test methods, and controlled procedures with precision and traceability., • Experience maintaining clean, safe, and compliant laboratory environments, including chemical handling, waste disposal, and equipment logs.Technical Documentation & Communication, • Strong ability to write lab reports, formulation records, test methods, and development summaries suitable for QA and regulatory review., • Skilled in maintaining batch sheets, and experimental documentation with auditready accuracy., • Ability to communicate technical findings to crossfunctional teams (R&D, QA, Regulatory, Manufacturing, Marketing). Hours: Contract position is 30 hours per week. For both roles, expectations for availability is during company work hours of 8:30 to 5:00 PM Pacific Time, Mon to Fri. Hybrid. 2 to 3 days a week can be remote, home office. Flexible schedule with availability for meetings and project coordination during normal business hours. Compensation: Salary ranges vary depending on experience level and if candidate is looking for part-time or full-time: | Senior Chemist | Part Time (Contract): $60k to $72k annual salary Full Time (Employee): $80k to $90k annual salary + benefits + initial LTI (Stock Option grants) | Manager, Prod Dev | Part-Time (Contract): $72k to $84k annual salary Full-Time: $90k to $110k annual salary + benefits + initial LTI (Stock Option grants) Support and Supervisor: Reports directly to the CEO and works closely with CMO, Chair of SAB, technical, manufacturing, quality, regulatory, and external development partners. Flexible work from home options available.

Job DescriptionAbout the Company e.l.f. Beauty, Inc. stands with every eye, lip, face and paw. Our deep commitment to clean, cruelty free beauty at an incredible value has fueled the success of our flagship brand e.l.f. Cosmetics since 2004 and driven our portfolio expansion. Today, our multi-brand portfolio includes e.l.f. Cosmetics, e.l.f. SKIN, pioneering clean beauty brand Well People, Naturium, high-performance, biocompatible, clinically-effective and accessible skin care, and our newest brand, rhode, a line of curated skincare essentials, formulated for a variety of skin types and needs with high performance ingredients, it’s a daily routine that nourishes your skin barrier over time. In our Fiscal year 25, we had net sales of $1 Billion and our business performance has been nothing short of extraordinary with 29 consecutive quarters of net sales growth. We are the #2 mass cosmetics brand in the US and are the fastest growing mass cosmetics brand among the top 5. Our total compensation philosophy offers every full-time new hire competitive pay and benefits, bonus eligibility (200% of target over the last six fiscal years), equity, flexible time off, year-round half-day Fridays, and a hybrid 3 day in office, 2 day at home work environment. We believe the combination of our unique culture, total compensation, workplace flexibility and care for the team is unmatched across not just beauty but any industry. Visit our Career Page to learn more about our team: https://www.elfbeauty.com/work-with-us rhode is seeking a Senior Research & Development Chemist, who is well versed in formulating personal care products, to join the team and play an integral role in formulating innovative products for our business. Reporting to the Director of Research and Development, you will be responsible for research, formulation, and managing cross-functional team projects. What You'll Do • Independently work on formulation projects based on product briefs provided by Product Development team, • Make batches of formulation projects, • Create formula revisions based on feedback from testing team, • Adjust batches as needed to meet formula specification requirements, • Maintain clear and accurate records of formulations, procedures, observations and results, • Prepare and log samples for submission, • Calculate appropriate specification ranges and create CofAs for formulas, • Conduct stability testing and keep accurate records, • Order raw material samples and maintain raw material storage room, • Request raw material documentation from vendors and maintain documents organized in shared folder, • Maintain formulation software, • Prepare bulk to be sent out to third party testing laboratories as needed, • Validate other chemist’s formulas, • Contribute to routine laboratory housekeeping and day-to-day operations of the laboratory, • Calibrate lab equipment, • Supervise scale up batches at Contract Manufacturers, providing instructions and recommendations as needed, • Communicate with Product Development, Operations, Quality, and Regulatory teams as needed, • Assist other lab staff as neededWhat You'll Bring, • Bachelor’s in Science in Chemistry, Chemical Engineering or equivalent, • 5+ years’ experience working as a formulation/bench chemist in a personal care formulation laboratory. Experience formulating OTC products - nice to have., • Must have experience using mixers, homogenizers, viscometers, and pH meters, • Strong knowledge of the following:, • Functionality of raw materials used in personal care formulations, • Ingredient listing, • Good Manufacturing Practices (GMP), • Experience maintaining a formulation software or database required (formula breakdown and entry of raw materials, including CAS, INCI, and cost information), • Experience using Microsoft Office (Outlook, Word, Excel etc.) or Google Workspace, • Highly organized, detail oriented, and able to independently manage multiple priority projects, • Must be a critical thinker and have strong problem-solving skills, • Agile and comfortable working in fast paced environment, • Must have strong communication skills and ability to explain technical information to a non-technical audience, • Willing to travel to contract manufacturer sites and supervise scale up batches as neededOther Details for Consideration Position is located: Santa Monica, CA Office requirement: 5 days in our Lab in Santa Monica Budgeted Salary Range: 105K-140K The base salary range for this role is listed above. Total compensation includes base salary, annual company-based performance bonus, and equity. Under e.l.f.’s annual bonus program, employees are eligible to earn up to 200% of their target bonus when company performance exceeds defined goals. In addition, e.l.f. provides a variety of other benefits to employees, including medical, dental, and vision insurance, a retirement savings plan, gender neutral parental leave, and unlimited paid time off. The amount of total compensation (including base salary) offered will be based on a wide range of factors, including geographic location, experience, specific skills, and qualifications. Compensation components are subject to change at the company’s discretion This job description is intended to describe the general nature and level of work being performed in this position. It also reflects the general details considered necessary to describe the principal functions of the job identified, and shall not be considered, as detailed description of all the work required inherent in the job. It is not an exhaustive list of responsibilities, and it is subject to changes and exceptions at the supervisors’ discretion. e.l.f. Beauty respects your privacy. Please see our Job Applicant Privacy Notice (www.elfbeauty.com/us-job-applicant-privacy-notice) for how your personal information is used and shared. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Job DescriptionDescription: AOCUSA | AMALIE OIL COMPANY IS HIRING IN CALIFORNIA Competitive pay and great benefits! AOCUSA pays the full cost of our Employee’s Health Insurance We are looking for a Lab Technician 1 for the following shift: First Shift: 6:00 AM PST – 2:30 PM PST Full-Time: Monday – Friday + Weekend Overtime as Needed OnSite: Vernon, California The right candidate will be trained for potential permanent/full-time employment. Amalie Oil Company is North America's largest privately held independent blender of motor oils and industrial lubricants. With production facilities in Tampa, Florida; Charleston, South Carolina; and the Los Angeles area, Amalie manufactures over 3,000 products and distributes to all 50 states and over 100 countries around the world. Better than it has to be... Since 1903. Are you looking for the right opportunity to establish your career? We are growing and need talented team players to join us! JOB SUMMARY Perform daily tasks involved in the laboratory operation as set forth by Shift Lead/Lab Manager. Essential Duties • Testing and documenting results of base oils, additives, blend samples, and production samples. (Final approval to remain with Chemist), • Creating and sending COAs for designated customers, • Assist with calibrating and/or standardizing instrumentation on a scheduled basis or as needed, • Keeping up with regular cleaning of the lab including glassware, testing benches, trash, and floors. Refilling necessary chemicals and dumping waste containers when needed, • Blending, testing, and recording data of hand blend formulations as generated by Chemist, • Maintaining sample integrity and organizing sample storage area •, • Retrieving samples from finished good tank Preferred Qualifications • Strong attention to detail, ability to use hand tools, and hard working., • Experience in quality control or similar tasks, • 1-year experience in a laboratory setting, • Use of general lab instruments, • Being able to communicate with team members on other shifts Work Environment + Physical Requirements The position is primarily within the laboratory and sample retain area; it involves standing, bending, squatting and climbing step ladders. Occasionally the technician will need to grab tank samples from finished good tanks. This position involves heavy lifting of about 50lbs Personal Protective Equipment • Slip-resistant, safety-toes shoes., • Eye protection., • Hearing protection. Equipment Used • Automated viscometers, • Density Meters, • X-ray, • Pour Point, • Colorimeter, • Mini Rotary Viscometer Compensation: · $24.00/hour Benefits AOCUSA pays the full cost of our Employee’s Health Insurance • Complete Insurance Coverage: Medical, Dental, Vision, Life and Supplemental Plans Available, • Full time, with full comprehensive benefit package that includes, Medical, Dental, Vision, Life, 401K, paid PTO and Sick time. Requirements:

Job Description Ready to take your career to the next level? Imagine working in a cutting-edge, brand-new facility where engineering, automation, and modern technology seamlessly come together. At AFF, you won’t just witness innovation—you’ll be part of it. We’re one of the fastest-growing companies of the last decade, and we’re just getting started. Our commitment to excellence, strong family-oriented culture, and passion for hiring top talent make AFF a standout place to build your future. For more than fifty years, American Fruits and Flavors has been creating unique fruit and flavor solutions for the food and beverage industry. Our reputation for creativity, innovation and technological advancement fueled our expansion into broader-based flavor capabilities. We are seeking a Flavor Chemist with over 10 years of experience creating flavors from flavor ingredients currently available worldwide. Must be strong in sweet/fruit flavors - namely berries, tropical, super fruits - and in unique non-characterizing flavors for use in food and beverage industries. Knowledge in savory a definite plus. Ability to create ethnic flavors and pair flavors together to create an impact on our customers. Must be well versed in keeping ahead of the trends and continuing to source the newest unique flavor ingredients available. Excellent communication skills are a must, with the ability to talk to top customers to determine real needs and convert the concept discussed into a tangible flavor that works and sells. Knowledge of US, EU, Asian, and/or South American regulations strongly desired. Knowledge of regulations of specific countries and regions worldwide also desirable. Must be able to work independently and as part of a team to accomplish the task at hand. We are seeking a competitive, driven, motivated individual who can step into our company and begin to produce immediately without disrupting the current system in place. Company DescriptionAFF manufactures custom juice and flavor blends for a wide variety of industrial users worldwide. Companies come to us for the latest and best ingredient blends and flavor systems for their products. In business over 50 years, we have two manufacturing plants and a distribution warehouse in Southern California. On April 1, 2016, American Fruits and Flavors was acquired by Monster Energy Company which expanded American Fruits and Flavors’ resources, significantly. American Fruits and Flavors, LLC is an equal employment opportunity employer and does not discriminate in hiring or employment upon any basis prohibited by law, including race, color, creed, religion, age, sex, national origin, cancer, genetic characteristics, genetic information, pregnancy, ancestry, sexual orientation, marital status, veteran status, or disability. None of the questions or information sought in this application is intended to discriminate based upon any status protected by law. Compensation Range: Actual salary/hourly wages are determined upon a variety of factors such as level of experience, skills, education and /or certifications, location, and position level AFF manufactures custom juice and flavor blends for a wide variety of industrial users worldwide. Companies come to us for the latest and best ingredient blends and flavor systems for their products. In business over 50 years, we have two manufacturing plants and a distribution warehouse in Southern California. On April 1, 2016, American Fruits and Flavors was acquired by Monster Energy Company which expanded American Fruits and Flavors’ resources, significantly.\r\n \r\nAmerican Fruits and Flavors, LLC is an equal employment opportunity employer and does not discriminate in hiring or employment upon any basis prohibited by law, including race, color, creed, religion, age, sex, national origin, cancer, genetic characteristics, genetic information, pregnancy, ancestry, sexual orientation, marital status, veteran status, or disability. None of the questions or information sought in this application is intended to discriminate based upon any status protected by law.\r\nCompensation Range: Actual salary/hourly wages are determined upon a variety of factors such as level of experience, skills, education and /or certifications, location, and position level

Job Description Job Title: Chemist II – Composite Materials (R&D) About the Role Dura Technologies is seeking a full-time, exempt Chemist II to drive the research, development, and optimization of our high-performance composite materials. Reporting directly to the Technical Director, you will lead multiple innovation projects, formulate cutting-edge material solutions, and collaborate with cross-functional teams. Your expertise will directly advance our position as a market leader in the aerospace, automotive, and marine composite industries. What You Will Do • Formulate Materials: Design resins, adhesives, and fiber reinforcements with enhanced mechanical, thermal, and chemical properties., • Lead R&D Projects: Spearhead research projects focused on developing novel composite materials based on market needs., • Conduct Lab Testing: Operate advanced lab equipment (e.g., Instron, QUV weathering testers) for tensile, flexural, and impact testing., • Troubleshoot Production: Investigate formulation or manufacturing issues using root-cause analysis and reverse engineering., • Manage Compliance: Assist the Operations Manager with government reporting requirements, including AQMD, CARB, Stormwater, and Hazardous Waste., • Maintain Documentation: Create and update SDS/TDS sheets, technical lab reports, and formula databases (ISO, ECC)., • Mentor Teams: Provide daily guidance and training to junior chemists and lab technicians to foster a collaborative environment. What We Look For • Education: Bachelor's degree in Chemistry, Materials Science, Chemical Engineering, or a related field., • Experience: 2 to 5 years of relevant industry experience in composites, polymers, paints, coatings, or materials development., • Testing Expertise: Proven familiarity with mechanical testing methods and physical property analysis., • Regulatory Knowledge: Strong understanding of chemical safety and environmental regulations (OSHA, REACH, RoHS, ISO)., • Leadership Skills: Proven track record of leading research projects and translating technical data into actionable insights., • Communication: Ability to write professional reports and present findings to vendors, customers, and management., • Physical Ability: Fully capable of working safely within both a laboratory and active production environment. Benefits & Compensation • Competitive Salary: Generous base pay matching your industry experience level., • Health Benefits: Comprehensive medical, dental, and vision insurance coverage options., • Retirement Plan: 401(k) plan with company matching contributions., • Paid Time Off: Generous vacation days, sick leave, and paid company holidays., • Career Growth: Continuous learning opportunities and direct mentorship from executive technical leadership.

Job Description Description SUMMARY The Polymer Development Chemist will be responsible for providing technical expertise in polymer chemistry processes, supporting day-to-day manufacturing operations, and ensuring efficient, high-quality production. This role involves hands-on troubleshooting, training, and continuous improvement initiatives. The ideal candidate will possess strong analytical skills, a deep understanding of polymer chemistry, and the ability to work effectively in a fast-paced manufacturing environment. You will also support the generation and review of batch records, technical summary documents to support the timelines of individual projects, and the investigation and documentation of any deviations in production. The scientist drives the implementation of new component systems, part changes, and other process related activities to support ongoing and new projects. This position will also help the production team in implementing manufacturing protocols and performing in-process testing of products. The candidate will follow SOPs and work in compliance with safety, regulatory and quality guidelines. What you will do: • Develop and optimize polymer chemistry processes and chromatography columns conditions to improve manufacturing efficiency and product quality. • Identify and implement process improvements to enhance safety, yield, and cost-effectiveness. • Provide day-to-day troubleshooting support to manufacturing teams to resolve process-related issues in real-time. • Work closely with production operators, engineers, and quality teams to address process deviations and ensure continuous production. • Develop and deliver training programs for manufacturing operators and technicians on polymer chemistry processes (column packing & testing), safety protocols, and equipment operation. • Serve as a subject matter expert for polymer chemistry within the manufacturing team, providing guidance and support as needed. • Collaborate with R&D teams to ensure smooth integration of new processes into manufacturing, providing feedback and recommendations to optimize scalability and manufacturability. • Collect, analyze, and interpret process data to monitor performance, identify trends, and drive data-driven decision-making. • Ensure all processes comply with safety, environmental, and regulatory standards. • Lead or participate in cross-functional teams focused on continuous improvement initiatives, including Lean Manufacturing, Six Sigma, and other process improvement methodologies. • Develop, review, and update Standard Operating Procedures (SOPs), batch records, and other process documentation to ensure clarity and accuracy. • Ensure that all documentation meets internal quality standards and regulatory requirements. How will you get here? Education Bachelor’s or Master’s degree in Chemistry or a related field, with a focus on polymer chemistry. Experience • 3 years of experience in process development, manufacturing support, or a related role within a chemical, polymer, or related industry. Academia Ok. Knowledge, Skills, Abilities • Strong understanding of polymer chemistry, manufacturing processes, and equipment. • Excellent problem-solving skills with a hands-on approach to troubleshooting. • Proven ability to analyze data and drive continuous improvement initiatives. • Experience in training and developing technical staff. • Strong communication and interpersonal skills, with the ability to work effectively in a team environment. • Knowledge of safety, environmental, and regulatory standards related to chemical manufacturing. • Proficiency in using process modeling and statistical analysis software is a plus. Job Type & Location This is a Contract position based out of Sunnyvale, CA. Pay and Benefits The pay range for this position is $30.00 - $40.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Sunnyvale,CA. Application Deadline This position is anticipated to close on Jul 15, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job DescriptionSalary: $90K-$95K, DOE Cogent Scientific, an insourced contract research organization, is looking for the right people to accomplish our Mission: to support the life sciences industry by cultivating and empowering exceptional scientists to deliver specialized laboratory services that advance research, foster collaboration, and accelerate innovation through quality and a shared commitment to excellence. We can offer you the chance to build on your skills and knowledge while working among experts in their fields and with cutting-edge instrumentation. Cogent Scientific offers competitive pay, attractive benefits (such as medical/dental/vision insurance; 401(k); parental leave; PTO and paid holidays; etc.) and an exciting work environment. This position may include relocation benefits as well. We aim to recruit the best people who stand out among their peers and embody our Core Values: Client Focused: We only succeed when our clients succeed. Outstanding: We deliver meticulous results through outstanding performance. Good: We act ethically and morally. Employee-Centric: We honor and support our employees. Nimble: We are prepared to adapt in an ever-changing industry. Team-Oriented: We collaborate with each other and with our clients. We currently have a role available for a Pharma Bioanalytical Chemistat our South San Francisco site. Job duties include, but are not limited to: • Supporting Bio-Analysis sample preparation, design and perform mass-spec analysis as well as data analysis/interpretation from in-vivo studies from triple-quad mass spectrometers (Sciex 7500), • Characterization of recombinant proteins, antibodies, and ADCs using intact-MS and peptide mapping for routine QC using high-res mass spec platforms (Orbitrap)., • Working closely with a team of scientists to support the development, optimization, and executing analytical assays for protein characterization and bioanalysis to guide large molecule therapeutic design., • Collaborating with the team to meet timelines and deliverables., • Performing general lab maintenance and instrument calibrations. Job requirements include, but are not limited to: • BS - Chemistry, Biochemistry or related field with 2-5 years industry experience or MS with 1-2 years industry experience in a mass spec focused lab on antibodies/ADCs/ proteomics or in a relevant scientific discipline focused on mass spec and ADCs., • Excellent communication skills verbal and written., • Works well both as a team and as an individual., • Demonstration of excellent team player skills, very strong attention to detail, very strong problem-solving skills, a high level of learning agility, and the ability to work across functions. The ideal candidate will be enthusiastic and self-motivated, with the leadership and communication skills necessary to operate effectively in a fast-paced multidisciplinary environment with flexibility and an adaptable approach to goal delivery. This is a day shift position (approx. 8a-5p local time). Cogent Scientific provides equal employment opportunities to all applicants and does not discriminate based on any legally protected characteristic. Additionally, if you require a reasonable accommodation during the application or interview process, please let us know. This job posting will remain open until 8/10/2026 or until a qualified candidate has been selected, whichever comes first.

Job Description PRST is seeking an experienced Shipyard Safety specialist to support operations at a busy yacht and shipyard facility in Alameda. This role is critical to maintaining a safe work environment for crews performing vessel repair, fabrication, and maintenance. This position is a temp to perm opportunity. The safety specialist will perform jobsite inspections, oversee confined space and hot work safety compliance, and act as a first responder for any jobsite injuries or incidents. This position works closely with supervisors, subcontractors, and shipyard personnel to enforce safety regulations and minimize operational risk. If you have shipyard, marine, industrial, or heavy construction safety experience, this is an opportunity to step into a high-impact role. Interested? Apply today or contact a recruiter at 510-227-7779. Responsibilities Conduct daily jobsite safety inspections across shipyard projects, vessels, and shop areas. Serve as a First Responder for jobsite injuries or medical incidents. Certify spaces for hot work and confined space entry on vessels and vessel components under repair. Perform air monitoring and atmospheric testing prior to work activities in enclosed or hazardous spaces. Follow and execute written and verbal direction from the Certified Marine Chemist regarding confined and enclosed space safety procedures. Provide daily inspections of confined, enclosed, and isolated spaces to identify hazards to personnel or equipment. Ensure all spaces cleared for entry meet safety requirements and are compatible with the work being performed. Monitor and enforce proper use of PPE, ensuring equipment is available and in safe working condition. Conduct specialized safety inspections, including: Fall arrest systems Confined space entry Scaffolding Lead abatement areas Document findings using inspection reports and coordinate with supervisors to correct any deficiencies. Ensure workers are properly trained and certified for the tasks they perform. Promote compliance with company policies and regulatory safety standards. Track and report near misses, incidents, and safety discrepancies according to the Field Safety Manual. Support ongoing improvements to the shipyard Safety & Environmental Program. Qualifications Previous experience in construction, shipyard, marine, or industrial safety environments. Knowledge of confined space entry, hot work permitting, and atmospheric testing procedures. Familiarity with OSHA safety standards and hazard identification. Experience performing jobsite inspections and safety reporting. Ability to work with diverse crews including contractors, vendors, and shipyard personnel. Strong communication and documentation skills. OSHA 30 Cert - REQUIRED #VHPAPandologic. Keywords: Industrial Safety Specialist, Location: Alameda, CA - 94501 , PL: 603784855

Job DescriptionBioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a Chemist III/Senior Chemist to work for a leading Orange County area biotechnology company.Pay Rate: $40-50/hourContract: 6+ months (with potential for conversion, but no guarantees)Mon - Fri with flexible shift hours! Can be 1st or 2nd shiftSummary:The Chemist III/Senior Chemist position will act as a senior member of the QC Analytical team, supporting raw material and finished product release, method qualifications (verifications, transfers, validations) and stability studies. The Chemist III/Senior Chemist will execute chromatographic (LC/GC), spectroscopic and wet chemistry testing. As a senior member of the team, the Chemist III/Senior Chemist will also assist with technical writing (Quality Investigations, Methods, Reports) and participate in lab improvement initiatives. Assists junior members of the team as chromatography trainer and technical expert.Responsibilities: • Independently execute QC chemistry testing to support routine manufacturing activities, new product method development and stability testing., • Review analytical raw data, • Participate in protocol design for qualification of new methods and subsequent authoring of new procedures., • Use technical expertise in LC/GC to troubleshoot new methods and improve existing procedures. Able to diagnose and make minor repairs., • Perform testing in compliance with relevant regulations. All activities are performed in GMP/GDP environment., • Assist in the performance of internal and external audits., • Assume role of SME and trainer for individual techniques/instrumentation, including chromatography., • Maintain the laboratory working areas in a clean and organized state., • Provide technical support to other departments within the organization., • Any and all other duties assigned by immediate supervisor.Experience/Requirements:, • Bachelors or Masters in Chemistry or related field, • 5-8+ years of experience in a Chemistry and GMP QC Laboratory, • Knowledge of quality systems, FDA and compendium requirements, • Experience executing method qualifications in a GMP environment., • Experience with various analytical instruments/techniques (chromatography, spectroscopy, wet chemistry, etc.)., • Demonstrated excellence in LC/GC analyses., • Experience with complex software programs preferred, but not required (Labware LIMS, Empower 3).Please send resumes to tiffany@biophaseinc.com and visit our website at www.biophaseinc.com for additional job opportunities!!!

Job DescriptionCompany Description ABOUT LGC BIOSEARCH TECHNOLOGIES: With manufacturing sites across the US, UK, Germany and Denmark, LGC Biosearch Technologies has plans to continue growing. We deliver mission critical genomics to our diverse customer base in molecular diagnostics, pharma/biotech and agrigenomics. Our integrated portfolio of products, services and expertise supports our purpose of Science for a Safer World and we have embodied our mission by working with customers to enable research into life-altering treatment for disease and illness worldwide. We are currently seeking candidates who are up for the challenge of operating in a high-growth, purpose-driven organisation. Job Description The role of an Senior Scientist, Oligonucleotide Chemist within the Innovation Hub team in Petaluma, CA, USA. Is to develop and / or improve synthesis, deprotection, purification, modification, and analysis methods and processes to enable the introduction of new oligonucleotide related products and the transfer of these into manufacturing. • Ensure compliance with safety regulations and Quality Management policies and processes., • Is the Technical Lead in Oligonucleotide NPD and / or custom / co-creation projects., • Collaborate with multidisciplinary teams to support both IH and Operations project deliverables., • Core function is to act as the technical oligonucleotide chemistry lead and contribute to the development and delivery of new oligonucleotide-based technologies and applications, • Demonstrated ability to independently design, project plan and execute development projects., • Independently develop synthesis methods to enable the delivery of custom / co-creation / NPD oligonucleotides using automated synthesizers and manual techniques., • Independently develop and optimize methods for oligonucleotide modification and conjugation (on-column and post synthesis and deprotection)., • Independently develop and optimize purification methods for various modified oligonucleotides and conjugates., • Perform analytical characterization of oligonucleotides using HPLC, mass spectrometry, and other relevant techniques., • Troubleshoot synthesis, deprotection and purification processes to resolve manufacturing issues and / or improve yield and quality., • Independently generate documentation package to support operations effective control and transfer into manufacturing, • Act as the subject matter expert post tech transfer and assist with chemistry troubleshooting., • Maintain accurate records of experiments and results in accordance with laboratory protocols, • Prepare technical reports and present findings to internal and external stakeholders. Effective communication at all business and technical levels.Qualifications, • Master's degree in chemistry or a relevant field plus a minimum of 10 years industrial experience in modified oligonucleotide chemistry or demonstrated equivalence., • Extensive knowledge and in lab practice with oligonucleotide chemistries, protocols and analysis. Demonstrated experience in synthesis, deprotection, purification, post synthesis conjugation techniques and analysis/characterization of oligonucleotides., • Proven expertise in using automated synthesizers and manual synthesis methods. Ideally with experience in a variety of synthesis platforms such as, but not limited to, MerMade, Dr Oligo, Shasta, K&A, OligoMaker, AKTA., • Full comprehension of all steps within the synthesis cycle and impact of changes to methods, cycle times and reagents to the fit, form and function of the oligonucleotide. Seasoned ability to predict oligonucleotide impurity profiles resulting from processing changes, • Full comprehension of all deprotection schemes and resulting chemical conformations and degradation products., • Full comprehension of non-compatible chemistry within the oligo and in subsequent processing., • Full comprehension of oligonucleotide purification chemistries, • Proficiency in analytical techniques, particularly HPLC and mass spectrometry., • Demonstrated extensive problem-solving experience., • Ability to optimize complex chemical processes and adapt to shifting priorities in a fast-paced, quality-driven environment., • Ability to make data driven recommendations and decisions., • Excellent data analysis and interpretation abilities, • Experience with quality control procedures and GMP regulations, • Understanding of nucleic acid therapeutics and diagnostics applications, • Ability to work efficiently in a fast-paced, collaborative research environment, • Strong organizational skills and attention to detail, • Excellent written and verbal communication skills in English Additional Information The typical pay range for this role is: Minimum: $93,750 Maximum: $156,250 This range represents the low and high end of the anticipated salary range for the California -based position. The actual base salary will depend on several factors such as: experience, skills, and location. ABOUT LGC: LGC is a leading, global life science tools company, providing mission-critical components and solutions into high-growth application areas across the human healthcare and applied market segments. Its high-quality product portfolio is comprised of mission-critical tools for genomic analysis and for quality assurance applications, which are typically embedded and recurring within our customers’ products and workflows and are valued for their performance, quality, and range. OUR VALUES • PASSION, • CURIOSITY, • INTEGRITY, • BRILLIANCE, • RESPECT EQUAL OPPORTUNITIES LGC strongly believes that every job applicant and employee should be valued for their individual talents regardless of age, disability, race, color, ethnic or national origin, sex, sexual orientation, gender reassignment, marital or civil partnership, pregnancy or maternity, religion, or belief. Short listing, interviewing and selection will always be carried out without regard to gender, sexual orientation, marital status, color, race, nationality, ethnic or national origins, religion or belief, age, or trade union membership. For more information about LGC, please visit our website www.lgcgroup.com #scienceforasaferworld

Job DescriptionWelcome to Beaker & Wrench, where we disrupt the status quo of processing equipment with our patented innovations and forward thinking improvements for optimal throughput. Started from the ground up by an engineer and a chemist, Beaker & Wrench is celebrating its 9th year in business in 2026. We are looking for an experienced Electro-mechanical Assembly Technician with attention to detail and a passion for high quality work to build our industrial processing equipment. The person in this role will join our skilled technical staff and will be required to work on-site Monday-Thursday 7:00am to 3:30pm. This position is hands-on, and requires a self starter with strong communication and organizational skills. If you're an enthusiastic team player who wants to be on the forefront of the technical equipment industry, Beaker & Wrench may just be the perfect fit for you! Responsibilities: • Build high-quality capital processing equipment to include: sanitary plumbing, motorized fluid and vacuum pumps, temperature controllers, wiring harnesses with soldered or crimped connections, and electrical control panels., • Read and interpret mechanical assembly drawings as well as electrical and piping schematics., • Provide attention to detail and follow all Quality Control requirements and checks so that all equipment that leaves the facility meets the high standards our customers have come to expect., • Follow SOPs to properly document manufacturing orders within the companies ERP system to ensure proper accounting for serialized and non-serialized inventory usage., • Keep the work area clean and all tools and supplies organized., • Ensure work is done safely and follows all OSHA and other safety standards., • Create, follow and help maintain Work Instructions (SOPs) related to Assembly and Build Procedures., • Knowledge and skill with industrial tools including water-jet cutter, saws, drills, wire strippers, soldering equipment, crimpers, grinders, plasma cutters, engraving tools, labeling tools, multimeters, and other basic hand tools., • Work and coordinate with other members of the team to help maximize productivity and efficiency., • Take on additional duties as needed by the team. Requirements: • High School diploma, associate’s degree, or trade school preferred., • 3-7 years of relevant work experience required, panel building experience highly desired., • Strong computer skills., • Attention to detail and organizational skills are essential., • Ability to collaborate and remain professional in a fast-paced environment., • Valid driver's license.

Title: Lab Pack Chemist Starting Pay: Up to $38/hr depending on experience Location: San Jose CA Contract to Hire - 6 month contract and then direct hire Qualifications: • BS degree in science or related with a desire to work in the Environmental industry, • 2+ years of lab pack experience, • Great communication and be able to work directly with clients, • Willing to get their hands dirty and work hard Managers Notes: • Will be working for one of their largest clients, • Will be working between 3 locations and will get paid mileage if they have to go between locations Benefits: • Health, Dental and vision insurance, • 401/k with contribution, • Tuition Reimbursement, • Health & Wellness including on location gyms, • Training, Training, and more Training, • They have a training schedule/program that everyone does and take 3 years and 120/hrs to complete, • PTO and Holidays, • Mentorship and career planning, • Auto/home insurance discounts Our client, who is one of the largest environmental services firms in North America is looking for Environmental Specialist to join their renowned team of professionals. They provide leading institutions in the higher education, life sciences, healthcare, and industrial sectors with diverse services and advice to assist them with compliance management. As an Environmental Specialist you will support our clients by managing their hazardous waste programs & projects, utilizing state & federal regulations. This is a labor-intensive role that requires a high-level of technical aptitude and the ability to deliver high-level customer service Essential responsibilities and duties: Technical: • Completion of on-boarding and Safety Training Development Program, • Safety equipment inspections, • Hazardous waste inspections, • Perform and document environmental health and safety (EHS) audits for clients, • Regularly preparing chemical and biological waste for shipment and disposal, including creation of all federal/state waste documents and managing the paperwork for the material, • Following any applicable state and federal regulations [Resource Conservation and Recovery Act (RCRA) & Department of Transportation (DOT) regulations], • Develop understanding of OSHA regulations as well as Health and Safety practices, • Monthly on-call responsibilities as part of our Emergency Response team Hands-on: • Material handling (e.g. transportation of materials within client sites as well as from client sites to transfer and/or end disposal facilities), • Safe handling of hazardous waste containers on client sites, as well as loading/unloading of waste from vehicles, • Packaging and prepping of hazardous waste for shipment, • Spill response measures, including assessment of the spills and potentially leading the cleanup efforts, • Requires you to work 40+ hours per week and overtime is frequently required Customer service: • Professional attitude, high energy, and high-level communication skills required when dealing directly with client representatives, • High level of expertise (e.g. state/federal regulations, EHS standards, waste management procedures, etc.), • Train clients on proper chemical safety and hazardous waste management, • Attending client operations meetings, • Training of new team member(s) Qualifications: • BS/BA in Environmental Science or Business-related degree or relative Military experience preferred, • Entry level - recent graduates accepted, • Valid driver’s license Ability to work as a member of a team as well as an individual #LI-JB1

Job DescriptionDescription: Batchmaker/Compounder Full-time Cypress, CA Description At ECOS®, we are a women-led company with a mission to create plant-powered laundry detergents and cleaners that are safer for people, pets and the planet. As a Climate Positive company, we restore more than 100% of its carbon, water, and energy use back to the earth, in our four manufacturing facilities right here in the USA. We have an immediate opening for Batchmaker to ensures the safe, quality, and consistent mixing of all production batches based upon orders received and stock levels. Key Job Functions: · Following batch making schedule and making all liquids necessary to fulfill orders · Taking all batch samples with corresponding batch sheet to Chemist for quality control · Reporting all problems and concerns with new and existing formulas to Chemist · Performing quality control in the lab as required to back-up Chemist and/or Lab Technician · Keeping all raw materials properly labeled and stored and in their proper location · Ensuring that all batch tanks, drums, pails, and lab samples are properly identified and labeled · Providing Purchasing with a weekly requisition for raw materials to be ordered · Reporting equipment breakdowns immediately to Plant Manager · Requesting all items needed to successfully perform job to Plant Manager · Ensuring housekeeping including a clean, organized batch area, in compliance with all safety regulations · Relocating chemicals received according to Deacom map · Handling other special projects and requests, as needed Requirements: In order to be successful, you will need: · High school diploma/GED · Forklift Certified · Familiarity with chemical blending, along with ability to follow product formula instructions and understand Safety Data Sheets. · Ability to safely lift bottles, boxes, tools, equipment, and other necessary items · Ability to multi-task · Ability to manage time effectively · Detail oriented with the ability to read, comprehend, and follow instructions · Ability to manage time effectively and multitask Starting Pay $23/hr Why join the ECOS Team: • Comprehensive group insurance including medical, dental, vision, short and long term disability, and supplemental insurance plans including accident and critical illness, • 401k with company match, • Paid vacation and sick pay, • Ten paid holidays per year including your birthday, • Paid parental bonding leave, • Sustainability incentives for purchasing eco-friendly car, • Wellness programs and incentives, • Equal Opportunity Employer/minority/female/disability/veteran

We are thrilled to announce the expansion of Garcoa’s Innovation Foundry at our Calabasas \n headquarters! We are not just expanding a department; we are building a dedicated space for \n Applied Innovation to redefine personal care and beauty standards. To support this growth, we \n are seeking a highly skilled and passionate Innovation Chemist—a creative builder who thrives \n at the intersection of bench science and emerging consumer trends. \n \n The ideal candidate will have a strong, hands-on background in cosmetic chemistry, with a \n focus on technology in skincare, haircare, body care, hot pours, and home goods. You will play a \n critical role in executing new formulations, developing innovative products, and translating \n forward-thinking trends into physical prototypes. \n \n Key Responsibilities: \n • Execute Innovative Formulation: Design, develop, and bench-test high-performance \n & head-to-toe formulations across multiple personal care categories. \n • Balance Creativity and COGS: Collaborate on turning blue-sky innovation concepts into \n mass-market viable products, respecting Cost of Goods Sold (COGS) targets during \n development. \n • Support Daily Lab Operations: Perform daily lab activities, including precise sample \n processing, raw material evaluations, and processing product development requests. \n • Testing & Quality Control: Conduct rigorous stability, compatibility, and QA/QC testing \n on new formulations, making technical adjustments to meet strict quality and shelf-life \n standards. \n • Cross-Functional Collaboration: Partner closely with Management, Product \n Development, Regulatory, and Production teams to ensure accurate product \n specifications and seamless manufacturing scale-up. \n • Apply Green Chemistry Concepts: Incorporate emerging technologies, sustainable \n ingredients, and green chemistry initiatives into everyday formulation tasks. \n • Rigorous Documentation: Maintain highly organized laboratory notebooks, \n documenting all phases of R&D including exact formulation procedures, test reports, \n and raw material data. \n • Technical Communication: Provide clear communication and technical feedback to \n internal departments and support client requests as needed. \n \n Requirements & Qualifications: \n • Experience: Minimum of 3 to 5 years of hands-on experience in head-to-toe \n formulation, with a track record of supporting products from bench concept to a high- \n volume marketplace. \n • Education: Bachelor’s degree in Chemistry or a related scientific discipline is preferred, \n but a proven ability to create without limits at the bench is highly valued. \n • Technical Proficiency: Deep expertise in cosmetic laboratory techniques, safety \n protocols, and standard laboratory instrumentation. \n • Industry Knowledge: Familiarity with cosmetic regulatory standards, OTC guidelines, \n and industry software tools (such as The Good Face Project platform). \n • Problem Solving: Strong analytical skills with the ability to work independently on \n formulation projects while remaining highly collaborative in a fast-paced environment. \n • Communication: Excellent verbal and written communication skills to effectively share \n technical findings with internal teams and stakeholders.

AMVAC®, an American Vanguard company, has successfully served the results-driven global markets through development, manufacturing and marketing of products for agricultural and commercial use. At American Vanguard, we believe in growth, innovation, and opportunity. We understand that a successful business is built on the strength of its people which is why we are dedicated to nurturing talent, fueling success and cultivating potential. \n \n AMVAC has a new opportunity for a Group Leader of Analytical Sciences. The Group Leader – Analytical Services provides strategic and functional leadership for the Analytical Sciences organization. This role serves as the company’s senior analytical chemistry expert, combining deep technical expertise with strong leadership to advance scientific excellence, operational performance, and global regulatory compliance across the product lifecycle. \n \n The Group Leader of Analytical Services will lead a high-performing team responsible for the development, validation, and application of sophisticated analytical methodologies supporting research and development, manufacturing, quality, and regulatory initiatives. This leader will drive innovation in analytical capabilities, oversee complex problem solving and technical decision-making, and ensure the highest standards of data integrity, laboratory compliance, and scientific rigor. \n \n As a key cross-functional partner, the Group Leader will collaborate closely with R&D, Manufacturing, Quality, and Regulatory Affairs to translate complex analytical findings into strategic business solutions that support product development, commercialization, and regulatory defense. This role also champions continuous improvement, laboratory modernization, and the development of scientific talent to strengthen organizational capability and long-term business success. \n \n Key Responsibilities \n\n • Functional & Technical Leadership: Provide direct supervision, mentorship, and career development for a team of scientists with advanced degrees. Foster a culture of collaboration, scientific rigor, innovation, and accountability\n, • Laboratory Strategy & Innovation: Evaluate and implement emerging analytical technologies and automation to enhance the laboratory’s capabilities and throughput\n, • Regulatory & GLP Excellence: Supervise the preparation and technical review of analytical data packages for global regulatory submissions (EPA, OECD). Ensure the lab maintains strict adherence to GLP (Good Laboratory Practices) and internal quality protocols\n, • Cross-Functional Integration: Translate complex chemical findings into strategic business recommendations for R&D, Manufacturing, and regulatory compliance teams\n, • Lead the analytical chemistry support function for Quality Control laboratories and cross-functional team needs, providing technical guidance, troubleshooting expertise, and strategic analytical chemistry oversight across the enterprise\n, • Strategic Method Development: Oversee the design and optimization of complex analytical methods (e.g., impurity profiling, structural elucidation, and trace analysis) using state-of-the-art instrumentation (such as HPLC/UPLC, GC, GC-MS/MS, LC-MS/MS, and Spectroscopy)\n, • Subject Matter Expertise: Act as the ultimate technical resource for troubleshooting complex analytical challenges and interpreting non-routine data for active ingredients and formulated products\n, • Resource & Project Management: Manage laboratory workflows, project timelines, and the analytical budget (CAPEX/OPEX), ensuring the team has the necessary tools and guidance to meet corporate milestones.\n, • Continuous Improvement: Drive a culture of continuous improvement, identifying areas for enhancement. Implement strategies to improve operational efficiency and economy\n, • Staying Informed: Keeping up to date with industry trends and scientific advancements.\n, • Comply with all regulatory requirements\n, • Align and comply with all company EH&S, CHP plans and policies\n, • Perform additional related duties as assigned by the supervisor\n\n \n Education Requirements \n\n • Ph.D. in Chemistry (Analytical Chemistry preferred) or a closely related scientific discipline\n\n \n Experience Requirements \n\n • 8 + years of postgraduate experience in an analytical sciences environment, ideally within the Agrochemical, Pharmaceutical, or Specialty Chemical industry\n, • 3 + years of demonstrated leadership. Proven track record of managing a technical team and leading functional lab operations\n, • Advanced Instrumentation Mastery: Expert-level proficiency in chromatography, mass spectrometry, and spectroscopy including structural elucidation of unknowns and complex matrix analysis.\n, • Regulatory Fluency: Significant experience with GLP/GMP/ISO standards and the requirements for global product registration\n, • Analytical Problem Solving: A history of resolving critical technical bottlenecks and managing non- conforming results through sophisticated root cause analysis\n, • Strong background in identifying and managing quality and compliance risks\n, • Excellent skills in leadership, project management, effective delegation, and budget management\n, • Excellent communication and interpersonal skills to influence and collaborate across the organization\n, • Willingness to travel up to 15%\n, • Ability to thrive in a dynamic and fast-paced environment.\n, • Proficiency in MS Office Suite (Outlook, Word, Excel and PowerPoint) is required\n, • Must also pass post-offer background check and other appropriate tests as required\n, • This position is fully on-site at the R&D facility in Commerce, CA\n\n \n \n OUTSTANDING BENEFITS \n American Vanguard provides Industry leading Medical, Dental, and Vision care with very low out of pocket premiums; Life and Disability Insurance for employees and family members; Health Savings Account (HSA) / Flexible Spending Account (FSA) options; 401(k) Retirement Savings Plan with employer match and Employee Stock Purchasing Plans. \n \n AMVAC is an equal opportunity affirmative action employer and values diversity in our company. We do not discriminate on the basis of race, color, religion, age, national origin, sexual orientation, gender identity or expression, marital status or domestic partnership status, disability, protected veteran status or military status, genetic information, or any other category protected under applicable law.

Dimension is looking for the company's first Environmental Field Chemist to join our team in San Francisco, CA. As the Environmental Field Chemist, you will be:.