Trabajos chemist en California

Process Chemist – Peptide / API Manufacturing LA County California (On-Site) $70/hour 6-Month Contract-to-Permanent Opportunity A leading peptide manufacturing organization is seeking a Process Development Scientist to support the advancement of innovative API processes from early development through full-scale cGMP manufacturing. This is a hands-on opportunity to work at the intersection of chemistry, process development, and commercial manufacturing supporting next-generation peptide and oligonucleotide medicines. The ideal candidate will bring strong synthetic chemistry expertise, process optimization experience, and the ability to collaborate cross-functionally in a fast-paced GMP manufacturing environment. Key Responsibilities • Develop, optimize, and scale synthetic processes for peptide and oligonucleotide APIs from lab through manufacturing, • Support technology transfer activities from Process Development into Production across internal sites, • Monitor and optimize chemical reactions, purification operations, isolation, and drying processes, • Perform and interpret analytical testing including High-performance liquid chromatography purification, in-process sampling, and related process analytics, • Troubleshoot process, equipment, and manufacturing challenges to improve efficiency and yield, • Partner closely with Production, QA, QC, Engineering, and Supply Chain teams to ensure compliant execution, • Author and review batch records, protocols, reports, SOPs, and technical documentation, • Drive continuous improvement initiatives focused on safety, right-first-time execution, and scalable manufacturing readiness Qualifications • PhD in Chemistry, Chemical Engineering, Organic Chemistry, or related discipline with 1+ year industry experience, • OR, • Master’s degree with 5+ years relevant industry experience, • Minimum 4+ years of industry experience in organic chemistry, process chemistry, or API development, • Experience with peptide chemistry, peptide manufacturing, or complex molecule synthesis strongly preferred, • Strong understanding of synthetic route development, scale-up, and process optimization, • Familiarity with cGMP environments, deviation management, and technical documentation, • Hands-on experience with analytical techniques such as High-performance liquid chromatography, UPLC, and reaction monitoring tools preferred, • Excellent troubleshooting, communication, and independent problem-solving skills Preferred Experience • Solid Phase Peptide Synthesis (SPPS), • Oligonucleotide API manufacturing, • Tech transfer between R&D and commercial manufacturing, • Purification, filtration, lyophilization, and drying operations, • Working in multi-site manufacturing environments Why Join • Contract-to-hire opportunity with long-term growth potential, • Work with a recognized leader in peptide manufacturing, • Direct impact on therapies advancing modern medicine, • Strong exposure to development through commercial-scale production

Job Description 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 Why join the ECOS family: Competitive wages starting at $22/hr Medical and dental insurance plans Paid vacation and holidays 401k Sick Pay Life insurance Paid maternity leave Equal Opportunity Employer/minority/female/disability/veteran Company DescriptionJoin the ECOS Team! 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.Join the ECOS Team! \r\n\r\nAt 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.

Principal Scientist, Medicinal Chemistry On site in San Diego, CA Status: Direct Hire | FTE Comp: 165-180k Role Summary We are seeking a senior medicinal chemist to play a central, hands-on role across all phases of small molecule drug discovery — from platform library expansion and hit identification through hit-to-lead progression and lead optimization — with the ultimate goal of driving programs to development candidate nomination and IND-enabling status. The ideal candidate brings deep synthetic expertise, a genuine comfort with ambiguity and novelty, and an appetite for continuous learning. This person will help shape program strategy while remaining willing to contribute at the bench when it matters most. Qualifications • PhD in synthetic organic chemistry with 4-8+ years of pharmaceutical or biotechnology industry experience in small molecule drug discovery, • Demonstrated understanding of program strategy and therapeutic hypothesis development, including assay relevance, clinical translatability, and the role of physicochemical properties in late-stage in vivo studies and clinical dosing, • Strong command of both classical and contemporary synthetic methodology and reaction mechanism, • Track record of applying ligand- and structure-based design principles to molecule crafting, leveraging the full breadth of available synthetic tools, • Proven ability to lead within and across integrated drug discovery teams, with at least one development candidate delivery as evidence of impact, • Experience mentoring junior chemists and managing external/outsourced chemistry partnerships, • Genuine enthusiasm for contributing to a fast-moving organization in whatever capacity the science demands — including direct laboratory work What We're Looking For Beyond credentials, we care about how you think and work: • Intellectual curiosity that drives you to ask better questions, • The confidence to take on problems without a clear roadmap, • Creative instincts that lead to non-obvious solutions, • Rigorous attention to detail at every stage of the work, • Willingness to question established thinking when the data warrants it

Analytical Chemistry Scientist II $36.25–$45.00/hr Mon-Fri 8am-5pm Onsite: San Diego, CA 92122 1 year assignment As an Analytical Chemistry Scientist II within Analytical Method Development and Transfer Group, you will play a key role in developing, validating, and, transferring analytical methods that support oligonucleotides synthesis and release testing, and raw material qualification. You will work in a fast ‐ paced, collaborative environment, partnering with cross ‐ functional teams to ensure high ‐ quality analytical support across multiple programs. This role requires deep technical expertise in chromatographic and spectroscopic techniques, strong problem ‐ solving skills, and hands ‐ on laboratory experience. Responsibilities: · Develop, optimize, validate and transfer analytical methods for oligonucleotides, raw materials, and reagent consumables. · Design, plan and execute various laboratory experiments with minimal supervision. · Prioritize multiple assignments and deliver high-quality results within established project timelines. · Analyze data analysis, interpret results, and troubleshoot unexpected analytical outcomes. · Prepare study protocols and reports, and assay work instructions with attention to details. · Ensure compliance with GMP, Good Documentation Practice (GDP), and quality standards. · Contribute to a positive, collaborative, and continuous-improvement-focused team culture. · Perform additional duties as assigned by manager. Requirements: · BS/MS/Ph.D in Analytical Chemistry, Chemistry, Biochemistry, Molecular Biology, or a related scientific discipline. · Minimum 2 years of hands-on experience in analytical method development, qualification, validation and transfer. · Proficient with analytical techniques including HPLC, LC-MS, UV-Vis, FTIR, Karl Fischer, and NMR. · Experience in analytical characterization and testing of oligonucleotides. · Demonstrated ability to perform and collaborative effectively across multidisciplinary teams. · Strong laboratory execution skills, including organization, documentation, and adherence to quality systems. · Excellent verbal/written communication skills. · Working knowledge of method validation principles and for regulatory expectations (FDA cGMP; ICH, USP). As an Analytical Chemistry Scientist II Analytical Method Development and Transfer Group, you will play a key role in developing, validating, and, transferring analytical methods that support oligonucleotides synthesis and release testing, and raw material qualification. You will work in a fast ‐ paced, collaborative environment, partnering with cross ‐ functional teams to ensure high ‐ quality analytical support across multiple programs. This role requires deep technical expertise in chromatographic and spectroscopic techniques, strong problem ‐ solving skills, and hands ‐ on laboratory experience. Responsibilities: · Develop, optimize, validate and transfer analytical methods for oligonucleotides, raw materials, and reagent consumables. · Design, plan and execute various laboratory experiments with minimal supervision. · Prioritize multiple assignments and deliver high-quality results within established project timelines. · Analyze data analysis, interpret results, and troubleshoot unexpected analytical outcomes. · Prepare study protocols and reports, and assay work instructions with attention to details. · Ensure compliance with GMP, Good Documentation Practice (GDP), and quality standards. · Contribute to a positive, collaborative, and continuous-improvement-focused team culture. · Perform additional duties as assigned by manager. Requirements: · BS/MS/Ph.D in Analytical Chemistry, Chemistry, Biochemistry, Molecular Biology, or a related scientific discipline. · Minimum 2 years of hands-on experience in analytical method development, qualification, validation and transfer. · Proficient with analytical techniques including HPLC, LC-MS, UV-Vis, FTIR, Karl Fischer, and NMR. · Experience in analytical characterization and testing of oligonucleotides. · Demonstrated ability to perform and collaborative effectively across multidisciplinary teams. · Strong laboratory execution skills, including organization, documentation, and adherence to quality systems. · Excellent verbal/written communication skills. · Working knowledge of method validation principles and for regulatory expectations (FDA cGMP; ICH, USP). Benefits:(employee contribution)  Health insurance  Health savings account  Dental insurance  Vision insurance  Flexible spending accounts  Life insurance  Retirement plan We also consider qualified applicants regardless of criminal histories, consistent with legal requirements. Pursuant to applicable state and municipal Fair Chance Laws and Ordinances, we will consider for employment-qualified applicants with arrest and conviction records. For Los Angeles, CA applicants: Qualified applications with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

Michelson Laboratories is a leading food testing laboratory based in Southern California. Since 1970, Michelson Laboratories has provided efficient testing and analyses to an extensive spectrum of customers. We have a broad-based background and are thoroughly proficient in a diverse range of industries. Our Chemistry Laboratory provides a wide range of services and is staffed with industry leading chemists. We are expanding our Chemistry department in our Commerce location and are looking for a Food Chemist. The Chemist will be responsible for performing analytical testing of food products. Responsibilities for Food Chemist: ·Review and approve data for Nutritional Labeling requests for various food products Perform titrations, extractions and analyze data for antibiotic residues, carcinogens, and other harmful chemical compounds -Troubleshoot and operate analytical instruments such as LC/MS/MS, HPLC, GC-MS, ICP-MS, ICP-OES, etc. -Troubleshoot or implement new test methods, ensure overall compliance to all regulatory and QA/QC requirements -Act as technical resource to other analysts within the department and to our clients -Prepare and review data packages/reports for reporting -Assist with special projects, method development and optimization -Review and update Standard Operating Procedures as needed. · Preparation of chemical reagents, standards, and samples for analysis · Maintaining detailed records of testing, quality activities, and chemical preparations · Ensure all analyses meet the turnaround time · Other duties as needed Qualifications for Analytical Chemist: · Master's Degree in Food Science, Analytical Chemistry, or other related sciences required. · Excellent interpersonal, verbal and written communication skills · Comfortable in a fast-paced environment with minimal direction and able to adjust workload based upon changing priorities · Ability to organize, prioritize and direct work activities; attention to detail · Time Management - ability to achieve results within expected time periods This Food Chemist position is a full-time position. Must have a flexible schedule and be available to work weekends, holidays and overtime as needed. Michelson Laboratories, Inc. is an Equal Opportunity Employer that does not discriminate on the basis of actual or perceived race, color, national origin, ancestry, sex, gender, gender identity, gender expression, pregnancy, age, veteran status, or any other legally protected status. Our management team is dedicated to this policy with respect to recruitment, hiring, placement, promotion, transfer, training, compensation, benefits, employee activities and general treatment during employment Job Type: Full-time Benefits: • 401(k), • Dental insurance, • Health insurance, • Paid time off, • Vision insurance Work Location: In person

We are seeking a highly skilled and passionate Innovative individual to join our company. The ideal candidate will have a strong background in chemistry, with a focus on technology in skincare, haircare, body care, hot pours, home goods and more, dedicated to a unique ability to be creative in all areas of development for personal care. You will play a critical role in the development of new formulations and ideation of innovative products and forward thinking. Key Responsibilities • Drive Innovative Formulation: Design, develop, and evaluate high-performance "head-to-toe" formulations., • Commercialize Creativity: Act as the bridge between blue-sky innovation and mass-market viability, treating Cost of Goods Sold (COGS) optimization as a creative challenge rather than a limitation., • Lead Daily Lab Operations: Manage all daily lab activities, including sample processing, data management, Quality Assurance/Control, and addressing product development requests., • Testing & Quality Assurance: Oversee and perform stability and compatibility testing on new formulations, making necessary adjustments to meet strict quality standards., • Cross-Functional Collaboration: Partner seamlessly with Management, Product Development, Regulatory, Quality, and Production teams to ensure product specifications are met and scale-up manufacturing is successful., • Champion Green Chemistry: Stay ahead of industry trends, emerging technologies, and regulatory requirements, with a strong focus on sustainable and green chemistry initiatives., • Rigorous Documentation: Maintain highly organized data, documenting all phases of R&D including formulation procedures, test reports, and final product specifications., • Customer Interaction: Provide technical support, expertise, and clear communication to both internal departments and external customers.Qualifications, • Experience: Minimum of 8 years’ experience in Head-to-Toe formulation, with a demonstrated track record of bringing products from concept to market in a fast-paced, high-volume marketplace., • Education: Bachelor’s degree in Chemistry is preferred but not strictly required. We are looking for someone who is unique and creates without limits on the bench., • Technical Proficiency: Deep expertise in laboratory techniques, equipment, and safety protocols., • Industry Knowledge: Strong familiarity with cosmetic industry regulatory standards, certifications, and The Good Face Project software., • Project Management: Excellent analytical, problem-solving, and project management skills with the ability to work both independently and collaboratively in an interdisciplinary environment., • Communication: Exceptional verbal and written communication skills, with the confidence to present to and interact directly with customers and key stakeholders.

Valo Health is a human-centric, AI-enabled biotechnology company working to make new drugs for patients faster.The company’s Opal Computational Platform transforms drug discovery and development through a unique combination of real-world data, AI, human translational models and predictive chemist

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 CDL A or B Sign-on Bonus $5,000 Clean Earth is a leading provider of environmental services in the United States providing remediation, disposal, recycling, and beneficial reuse solutions for hazardous and non-hazardous waste, contaminated soil, and dredged material. Our vast portfolio of technologies and services touches nearly every industry that generates waste including energy, infrastructure, commercial, industrial, retail, and healthcare markets. Every day our teams across the country take a hands-on, dedicated approach to recycling and beneficially reusing waste that would otherwise go into landfills. We value our employees as our most important asset, and this is reflected in many areas across our company including recently being named a 2024 Most Loved Workplace ®. We are committed to creating a positive work culture that fosters growth and development while ensuring the health and safety of our employees. 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 Starting pay $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 Clean Earth offers competitive benefits including health, dental, vision, life, and disability insurance plans starting on the first day of employment; paid time off, wellness benefits, employee discount program, and tuition assistance. We provide equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, veteran status, gender identity, or genetics. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. If you have a difficulty applying for any job posted on Enviri Clean Earth’s website because a disability prevents you from using the online system, Clean Earth offers the following alternate application procedure: Call toll free (833) 209-2659 and leave your name, phone number, city and state of residence. Clean Earth will arrange for an alternate method of applying and will consider your application together with all other applications received for the job. This line is dedicated to disability applications only. No other inquiries will receive a response. Military veterans encouraged to apply

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 Description ABOUT THE ROLE We are seeking a motivated and detail-oriented Junior Analytical Chemist to join our growing laboratory team. This is a bench-focused, hands-on role supporting sample preparation, routine testing, and data generation within a regulated GMP/GLP environment. You will work alongside experienced scientists to build practical analytical skills and contribute directly to client project deliverables. KEY RESPONSIBILITIES • Perform routine analytical testing using established methods, including HPLC, GC, LC/MS, ICP-MS, and ELISA, • Prepare samples, reagents, and standards in strict accordance with written Standard Operating Procedures (SOPs), • Execute experiments and assays following pre-validated protocols with accuracy and consistency, • Record, document, and report data in laboratory notebooks or electronic LIMS systems, • Assist with data analysis and result summaries under the direction of senior scientists, • Support routine maintenance, calibration, and basic troubleshooting of analytical instrumentation, • Maintain a clean, organized, and compliant laboratory environment aligned with safety and quality standards, • Contribute to SOP updates and technical documentation as needed, • Collaborate effectively with cross-functional team members to support project timelines and deliverables QUALIFICATIONS Required: • B.S. in Chemistry, Biochemistry, or a closely related scientific discipline, • 1–2 years of laboratory experience (industry preferred; exceptional academic experience considered), • Hands-on familiarity with analytical instrumentation, including HPLC, GC, and UV/Vis spectroscopy, • Strong attention to detail with the ability to follow defined procedures and protocols precisely, • Ability to manage multiple samples and concurrent tasks in a fast-paced laboratory environment Preferred: • Exposure to or foundational knowledge of GMP/GLP regulatory environments, • Experience with LIMS or electronic laboratory notebook (ELN) systems, • Familiarity with LC/MS, ICP-MS, or ELISA techniques WHAT WE OFFER • Hands-on experience with cutting-edge analytical instrumentation in a regulated CRO environment, • Mentorship from experienced analytical scientists committed to your professional growth, • Exposure to diverse biopharmaceutical projects across multiple therapeutic areas, • A collaborative, science-driven culture focused on quality and innovation, • Competitive compensation and benefits package 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 - $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 Hercules,CA. Application Deadline This position is anticipated to close on May 31, 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. 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 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 Description Job ID: 71687 Location: Raritan, NJ Pay Rate: $46/hr. Contract: 7 Months (Renewable) • Role would be considered an Analytical Chemist, • Onsite 100% of the time in Raritan, NJ, • Could be extended into 2027, • Must have at least 4 years of experience, • Bachelors degree required, • Must have GXP lab and GMP experience, • Will be testing and validations, • Chromatography and chemistry work, • Working knowledge of acid, moisture testing (autotiration), • Experience with liquid chromatography (LC, GC), • IV experience ideal, • Must have analytical chemistry experience, • Inherent viscosity experience Top 3 non-negotiable skills: • Chromatography, • Inherent viscosity experience, • Wet Chemistry experience Description: Overall Responsibilities You will join the Analytical Characterization group within the company’s research and development organization. You will become part of the chromatography and wet chemistry laboratory (GxP lab) for the qualitative, and quantitative analyses of small organic compounds, additives, degradation products, and impurities in complex polymer matrices. You will stay ahead of new scientific and technological developments in the field of chromatography and continuously improve the organization’s capabilities in support of New Product Development and Life-Cycle Management. You will perform hands-on experiments independently while collaborating with other analytical associates. Key Responsibilities: • Perform analysis with chromatography techniques (U/HPLC-UV/MS and GC, GC Headspace) and other wet chemistry techniques (KF, Autotitration, water content, and water solubility) on various materials and chemicals., • Perform workflow including sample preparation, method execution/ qualification, data acquisition, analysis and reporting as per appropriate protocols., • Reports issue to management and participate in issue resolution, such as reporting OOS/OOT results, participating in laboratory investigations, reporting instrument issues, troubleshooting instruments, etc., • Practices safe and environmentally sound laboratory techniques adhering to regulatory, local government, and safety guidelines., • Communicates clearly and concisely, through verbal and written reports, the results of assigned tasks., • Maintains secrecy of confidential and sensitive information by observing all procedures regarding securing and transmitting privileged information., • Maintain good documentation and lab notebook per company procedures, and FDA/ICH guidelines., • Assists senior staff in the preparation of technical reports and manuscripts., • Responsible for ensuring personal and Company compliance with all Federal, State, local, and Company regulations, policies, and procedures, • Performs other duties assigned as needed Qualifications Education: • BS, MS, or Ph.D., in Chemistry (Analytical, Polymer, or Organic preferred), or related science degree., • 4+ years of experience with a BS degree, 1+ years of experience with a MS degree, 0+ years of experience with a Ph.D., • Practical knowledge of medical device regulations. Experience and Skills: • Hands-on experience with HPLC, GC, and other wet chemistry techniques are required., • Experience with analytical test method development and validation is preferred., • Experience in an Analytical Laboratory with GMP or quality control setting is preferred., • Work independently and also effectively collaborate and communicate with other team members., • Displays passion and enthusiasm for innovation., • Experience with Viscosity testing (Inherent, Brookfield) Company Descriptionwww.techdataservice.comwww.techdataservice.com

Job Description Job Description We are seeking a skilled Chemist to join our team and assist in applications development. The role involves preparing samples, performing analytical tests, recording data and observations, and preparing summaries of experiments. You will also perform both manual and automated die bonding applications, troubleshoot basic process issues, and escalate them as needed. Additionally, you will perform parameter optimization and failure analysis, handle microscopic components using microscopes, tweezers, and vacuum tools, and ensure process documentation, basic troubleshooting, maintaining repeatability, and yield are upheld. Responsibilities • Assist in applications development by preparing samples and performing analytical tests., • Record data and observations, and prepare summaries of experiments., • Perform die bonding applications both manually and automatically., • Troubleshoot basic process issues and escalate them appropriately., • Perform parameter optimization and failure analysis., • Handle microscopic components using microscopes, tweezers, and vacuum tools., • Ensure process documentation, basic troubleshooting, maintaining repeatability, and yield. Essential Skills • At least 1 year of industry experience in a related field., • Technical certification or degree in a related field., • Experience in materials testing, working with metals, quality control, or lab experience., • Basic computer skills including Microsoft Excel, Word, and PowerPoint., • Ability to log process data., • Strong attention to detail with a focus on process control and documentation., • Ability to work in a team environment and communicate effectively. Additional Skills & Qualifications • Familiarity with statistical analysis software such as Minitab is a plus., • Hands-on with good time management skills., • Ability to follow instructions and maintain quality., • Physical ability to stand, reach, use fine tools, and occasionally lift small weights or handle assemblies. Work Environment This role is based in a lab environment. Our organization offers a small company feel with big financial backing, fostering a great culture where everyone is supportive and gets along well. Job Type & Location This is a Contract to Hire position based out of San Jose, CA. Pay and Benefits The pay range for this position is $26.00 - $32.00/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 Jose,CA. Application Deadline This position is anticipated to close on May 31, 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. 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:\n\nCompany Description Eurofins Scientific is a network of independent companies providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. With more than 20 U.S. locations, Eurofins Built Environment Testing offers Industrial Hygiene (IH) and Indoor Air Quality (IAQ) services to protect health in built environments. Clients include consultants, industry, real estate, healthcare, government, and homeowners. Services cover a wide range of tests, including asbestos (PLM/TEM), mold, bacteria, VOCs, allergens, Legionella, radon, lead, silica, and more.Job Description Eurofins Environment Testing Northern California is looking for a Project Manager Associate in our Folsom, CA location. Under general direction, the Project Manager Associate communicates with clients in a professional and timely manner to build and maintain strong customer relationships. This role proactively manages and tracks projects from initiation through completion, escalating issues to management as needed. The position requires the ability to efficiently prioritize responsibilities with a proactive approach, strong attention to detail, and awareness of issues impacting both internal and external stakeholders. The Project Manager Associate must be able to listen effectively, influence others toward desired outcomes, and maintain an approachable and open demeanor while supporting key functions including project setup and maintenance, login review, client account management, reporting, invoicing, bottle orders, and identification of appropriate work-share facilities. Key Responsibilities: Project Setup & DocumentationReview project in LIMSCreate and configure projectAdd project notes (special reporting, invoicing instructions, etc.)Upload all project documents to the central repositoryManage purchase orders, task orders, and change order requestsVerify that lab compound lists and limits meet project requirementsAdd project-specific limits/lists to LIMSAssign deliverables and delivery routesCommunicate project details to operationsEngage workshare labs, service centers, or non-Eurofins Environment Testing locationsWork with operations to ensure adequate capacityProvide updates to operations on upcoming work.Create bottle orders.Schedule courier or field sampler when needed.Confirm subcontract labs are approved and properly set up as vendors (for new and existing work).Initiate approval process for subcontract labs not on the approved list.Generate subcontract paperwork.Create requisitions in accounting software for subcontracting work.Verify lab certifications and limits meet project requirements.Confirm EDD format availability for new quotes; submit helpdesk ticket if a new format is required.Provide client support documents as needed (contact lists, bottle tables, preservation tables, etc.). Sample ReceiptCommunicate issues to clients throughout the projectManage incoming work for rush and short-hold samplesReview log-inResolve log-in discrepancies with clientInform client of any log-in issuesSet samples to “available” after reviewSend sample receipt confirmation to client ReportingUnderstand client-specific reporting requirementsReview job list daily and manage due datesNotify clients of any expected delays prior to the due dateConfirm data anomalies with operations (e.g., filtered > dissolved, deviations from historicals)Review reports and EDDs before submissionConfirm correct report format and EDD formatIssue final reports by client due datesIssue final data packages InvoicingSet up delivery routesReview final invoice before issuing it to the clientGenerate credit/debit memos as neededSubmit credit/debit memos for approval and send approved versions to the client when applicableSubmit revised invoices when corrections are requiredFollow up with clients to confirm accurate invoicingWork with collections on A/R follow-upConduct regular reviews of A/R status Client Set-UpWork with CSM to communicate lab capabilities to the clientSubmit new client review requestsConfirm sales assignments with the Business Development Manager and Account ExecutivesReceive new quote requests from clientsReview client contract requirements with CSM, Lab Director, and othersReview and submit purchase orders for approvalFollow up on client terms and credit limits Account MaintenanceConduct follow-up calls and client visits as neededSubmit client complaints and participate in corrective actions and follow-upCommunicate client issues/complaints to salesFollow up on client requests, including technical supportUse internal resources to resolve client needs efficientlyMaintain familiarity with company capabilities and key contactsForward opportunities and leads to salesForecast upcoming work Quotes & ProposalsRequest technical support from operations (special requests, method development, technical reviews)Generate quotes and obtain approvalsReview client quote requests for capabilities, certifications, and scopeConfirm client contracts and pricingDetermine appropriate lab placementVerify that lab certifications, compound lists, and limits meet project requirementsPrepare and submit quotes for approvalSend approved quotes to clientsForecast and track quotes in LIMSProvide QAPP/SOW information to clients as neededUpdate project status in LIMS Other ResponsibilitiesPerform other duties as assigned by leadershipQualifications Basic Minimum Qualification:Bachelor’s degree in Environmental Science, Chemistry, Engineering, or a related field.Experience managing client accounts and delivering multi-phase analytical projectsProject Management Professional (PMP) Certification or similar project management certification is a plusFamiliarity with EPA and Toxic Organic methods and regulationsPrefer 1+ years bench Chemist experience in air analysis or field experience.Authorization to work in the United States indefinitely without restriction or sponsorshipProfessional working proficiency in English is a requirement, including the ability to read, write and speak in English Skills and AbilityStrong Interpersonal Skills: Builds positive relationships with clients, colleagues, and stakeholders at all levels, fostering trust and collaboration.Effective Communication: Clearly and confidently conveys information both verbally and in writing; tailors communication style to diverse audiences and situations.Problem-Solving & Critical Thinking: Proactively identifies challenges, analyzes root causes, and develops effective, practical solutions.Time Management: Demonstrates the ability to manage multiple projects simultaneously, prioritize tasks, and consistently meet deadlines and deliverables.Organizational Skills: Maintains accurate records, manages complex workflows, and ensures projects and documentation are handled efficiently and thoroughly.Client Service Excellence: Demonstrates a proven ability to deliver exceptional client experiences by anticipating needs, resolving issues promptly, and providing ongoing support.Leadership: Guides teams and cross-functional stakeholders toward common goals; inspires collaboration, accountability, and high performance.Technical Proficiency: Proficient with standard business and project management tools, including Microsoft Outlook, Word, Excel, PowerPoint, and Access.Multitasking & Prioritization: Efficiently handles competing priorities without compromising quality, accuracy, or deadlines.Adaptability & Flexibility: Adjusts quickly to evolving client needs, project scopes, and organizational priorities in a fast-paced environment.On-Time Delivery: Consistently meets or exceeds deadlines and client expectations by managing schedules, resources, and dependencies effectively.Client Focus: Demonstrates a strong desire to understand and meet customer needs. Actively listens, asks clarifying questions, and follows up during and after projects. Keeps clients informed of key decisions, seeks feedback, and adjusts services to enhance satisfaction and outcomes.Technical Understanding: Seeks and applies information from various sources to address client technical inquiries confidently and communicate project status accurately.Customer Service Orientation: Strives to exceed customer expectations and takes ownership of resolving issues. Provides prompt, thorough, and accurate information, informs clients of commitments and performance guarantees, and proposes appropriate solutions or services. Sets clear and professional boundaries when necessary. Additional Preferences:Knowledge of federal, state, and local air quality regulations (EPA, CARB, NESHAP, MACT) and their implications for analytical projects.Familiarity with air testing methods and environmental laboratory workflows.Familiarity with ISO 17025, TNI, DoD ELAP, and other quality standards relevant to environmental laboratory operations.Understanding of key financial principles such as invoicing, AR managementDemonstrated success in nurturing client relationships, identifying cross-selling opportunities, and contributing to revenue growth strategies.Ability to work effectively with technical operations, QA, field services, sales, and finance teams to deliver seamless client experiences.Additional Information Compensation Range: $26-$28 per hour depending on experience and qualifications. Position is full-time, Monday - Friday, 8:00am - 5:00pm with weekends and overtime as needed. Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base compensation may vary based upon, but not limited to, relevant experience and skill set, base compensation of internal peers, business sector, and geographic location. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options. We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! At Eurofins, we believe sustainability is at the heart of everything we do. Guided by our vision to be the Global Leader in “Testing for Life,” our mission to contribute to a healthier and safer world, and our core values, we are building a strong foundation for Environmental, Social, and Governance (ESG) initiatives. Eurofins’ commitment to sustainability begins within our own companies through a shared responsibility to people and the planet. With climate change posing an imminent threat, Eurofins and its many companies recognize their duty to proactively reduce or offset the environmental impact of essential operations while also helping our clients do the same—serving as a true ESG Enabler. Find out more in our career page: https://careers.eurofins.com/ Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2025, Eurofins generated total revenues of EUR 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

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 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 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 POSITION SUMMARY: Under limited supervision, the Chemist III is responsible for performing routine analytical testing, supporting non-routine chemistry and development projects, method development/validation/transfer activities, preparing technical documentation, and maintaining laboratory equipment in the quality control analytical laboratory. RESPONSIBILITIES: • Perform routine laboratory testing (i.e., HPLC, LC/MS, UV-Vis, FTIR, CE, KF Titration, INSTRON, osmolality, pH, color/clarity, CCIT, particulate matter, wet chemistry) including finished product release, stability studies, and raw materials, following SOPs and GMP requirements., • Author and execute protocols for method transfer, qualification, and validation., • Support method development, non-routine projects, and analytical tech transfer/feasibility studies., • Perform technical evaluation of complex analytical data. Create data summaries and author technical reports., • Develop, author, and revise SOPs, as needed., • Train and guide junior chemists., • Assist with routine testing for WFI samples, including TOC, conductivity, and endotoxins, as needed., • Perform QC peer-review of laboratory raw data., • Calibrate, maintain, and troubleshoot various complex instruments such as HPLC, LC/MS, GC, UV/SoloVPE, etc., • Initiate problem-solving for technical issues commensurate with level of experience., • Assist with the implementation of new equipment, instruments, and software., • Support quality system activities, such as deviation investigations and laboratory OOS/OOT investigations. QUALIFICATIONS AND EXPERIENCE: • Bachelor’s or advanced degree in analytical chemistry, biochemistry, or a related field, • 7+ years (with Bachelor’s) or 4+ years (with advanced degree) of analytical quality control experience in a cGMP setting, covering early and late-phase products., • Strong knowledge of and hands-on experience with analytical techniques such as HPLC, GC, UV-Vis, mass spectrometry, and other common analytical equipment and techniques., • Experience with method development, technical writing, and executing method validations/ method transfers.

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 Description Ready to take your HPTLC expertise to the next level and make a measurable impact in a growing lab environment? Tentamus California is searching for an HPTLC Chemist to support advanced analytical testing of botanical materials, dietary supplements, and natural health products. This role requires strong expertise in high-performance thin-layer chromatography (HPTLC) and complementary analytical techniques, with a focus on method development, validation, and regulatory compliance. Experience in botanical analysis and manufacturing environments is strongly preferred. WHAT YOU'LL DO As the HPTLC Chemist, reporting to the Lab Manager, your responsibilities include (but are not limited to): • Perform qualitative and quantitative analysis of botanical and related products using HPTLC and other analytical techniques, • Develop, validate, and optimize analytical methods in accordance with regulatory and internal standards, • Operate, maintain, and troubleshoot laboratory instrumentation (HPTLC, HPLC, LC-MS, GC-MS, GC), • Conduct botanical identification using established methods and reference standard libraries, • Analyze and interpret complex data sets, ensuring accuracy, integrity, and compliance, • Prepare technical reports, validation protocols, and documentation for regulatory and client requirements, • Support testing of dietary supplements, natural health products, and, where applicable, pharmaceutical products, • Collaborate cross-functionally with quality, production, and R&D teams, • Ensure adherence to applicable regulatory standards (e.g., FDA, ICH, ISO 17025) and internal quality systems, • Mentor junior staff, support team development, and contribute to project planning and execution SCHEDULE & POSITION This is a full-time, onsite role located at Tentamus California 133 Technology Dr #150, Irvine, CA 92618. The schedule is M-F 9AM – 5PM with the occasional weekends required. WHAT'S IN IT FOR YOU? Tentamus offers an annual salary between $65,000 - $78,000, plus a comprehensive, low-cost, benefits package, including medical, dental, vision, disability, and life insurance. Employees also enjoy paid time off (PTO), 40 hours of sick time per California State Law, a matching 401k plan, and access to our free Employee Assistance Program! QUALIFICATIONS The ideal candidate will be authorized to work in the United States indefinitely and without restrictions or sponsorship, hold a Bachelor's Degree in Chemistry, Microbiology, or related life science and/or with experience in analytical laboratory testing will be considered; and who meets the following qualifications: • BS degree in Chemistry, Biology, or related field., • Minimum of 3 – 5 years of hands-on analytical laboratory experience, preferably in pharmaceutical, biotechnology, or related industry., • Minimum 1 - 2 years of hands-on HPTLC experience highly preferred., • Experience with analytical method development and/or validation preferred, • Expertise in a wide range of analytical techniques and instrumentation, with proficiency in method optimization and troubleshooting., • Familiarity with regulatory standard requirements (e.g., FDA, ICH guidelines, ISO 17025) and experience with regulatory submissions., • Excellent data analysis skills, including proficiency in statistical analysis software, • Leadership or mentorship experience is a plus., • Effective communication skills, both verbal and written, can convey complex technical information to diverse audiences., • Detail-oriented approach with a commitment to quality, safety, and compliance., • Instrument maintenance and troubleshooting experience 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 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 DescriptionCertified 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. M-F 8AM-5PM

Job DescriptionBenefits: • Life Insurance, • LTD, • 401(k), • 401(k) matching, • Dental insurance, • Health insurance, • Paid time off, • Vision 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 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 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 A leading innovator and manufacturer of specialty coatings for use by professionals in the design and construction industry. For over 40 years, we pioneered new formulas and systems specifically for waterproofing, epoxy, surface, and texture coating applications. Westcoat, our comprehensive four-category line of coating products, take the guesswork out of selecting the best system for each project. Westcoat's proprietary formulas, tested through rigid applications in all environments, are made to adhere with long-lasting, durable results. Delivering numerous protective, textured, and decorative options. JOB DESCRIPTION Paint & Coating Chemist San Diego, CA Reports to: Technical Director FLSA Status: Full-Time Exempt Supervisory Responsibilities: None Position Overview As a Paint & Coatings Chemist you will perform chemical and physical tests on existing and newly developed products, raw materials, and evaluate results to determine if products meet Westcoat specifications. The primary purpose of the Chemist is to design and implement methods for process control, process improvement, testing, and inspection to ensure quality control standards, color matching, and coating formulation to promote and uphold Westcoat's superior specialty coating systems. Location This position is based at our headquarters in San Diego, CA and is fully onsite. The anticipated work hours are from 7:30 AM to 4:00 PM, with occasional overtime needed to fulfill production obligations and meet business requirements. ESSENTIAL DUTIES AND RESPONSIBILITIES The essential functions include, but are not limited to the following: • Designing and implementing methods for process control, process improvement, testing, inspection to compliance, safety, and product/material specifications., • Owning, promoting and executing quality standards, inspection processes, testing methodology, quality plans, utilizing proper documentation, and reporting methods., • Interfacing with supplier and customer quality representatives concerning problems with quality assurance and ensuring that effective corrective action is implemented., • Formulation development and improvements as directed by Technical Director or Westcoat leadership team., • Owning and participating in cost reducing studies of various product lines to achieve quality standards amidst cost reduction strategies., • Compiling, writing, and delivering training material on quality standards and activities, • Assisting in process certification as assigned by Technical Director or Plant Manager., • Color adjustments of specification production batches of coatings and achieving color matching of custom colors and all documentation related to said function., • Developing, executing, and analyzing quality-reporting measures & making proper adjustments or recommendations as deemed necessary., • Reporting to management on quality issues, trends and losses., • Participating in internal and external quality audits., • Upholding a clean and organized laboratory environment in alignment with manufacturing and safety protocols., • Perform additional duties as assigned. Qualifications & Skills • Bachelor's degree in chemistry, Engineering or related field with strong understanding of organic and analytical chemistry., • Strong synthetic skills and knowledge of coating lab techniques., • Adaptable and flexible, able to handle multiple demands and shifting priorities., • Self-motivated with good interpersonal skills and ability to work effectively in a fast-paced, collaborative environment., • Able to document and present findings clearly through End of the Day reports, and presentations., • Proficiency in reading and understanding laboratory & manufacturing-related documents, including lab records, SOPs, standards of quality and protocols., • Strong analytical skills, mathematical aptitude, and effective time management abilities, with the capability to multitask while prioritizing safety., • Excellent oral and written communication skills., • Ability to work both independently and collaboratively within a team environment. Working Conditions: You will be working in a general laboratory and manufacturing environment, with regular exposure to bulk paint and other chemical products. The workspace may experience temperature fluctuations based on outdoor conditions. You may also encounter minimal levels of airborne dust. At times, the factory or production area may be loud, humid, cold, or hot, consistent with a typical manufacturing environment. Benefits and wages: • Starting base pay ranges from USD $70,000 to $120,000 annually based on experience., • Comprehensive medical, dental, and disability benefits programs., • Company-sponsored 401(k) plan with a matching contribution., • Eligibility for employer discretionary profit-sharing contribution for all eligible employees, based on various factors determined by the organization., • Paid time off accrual plan, along with paid company holidays., • Employee perk program for exclusive employee savings to theme parks, hotels, gyms, rental cars, sports, concerts, etc. Note: This job description is intended to provide a general overview of the position's duties and responsibilities and is not exhaustive. Duties, responsibilities, and requirements may change over time and may vary based on business needs. Employment with Westcoat Specialty Coating Systems is at-will, in accordance with California law, meaning either the employee or the company may terminate the employment relationship at any time, with or without cause, and with or without notice. This job description does not constitute a contract of employment, implied or otherwise. All employees are required to comply with company policies and procedures. This job description may be revised at any time at management's discretion. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the position. The pay range for this role is: 70,000 - 120,000 USD per year (San Diego)

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 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 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 DescriptionFurientis is building a new class of defensive interceptor missile for the United States and its allies. We design, build, and produce these systems end-to-end, from physics through manufacturing, at production rates legacy primes cannot match and at a fraction of the cost. We recruit engineers who internalize the warfighter's problems and bring deep mastery of the relevant technologies, without the institutional inertia that has slowed the legacy primes. Work done at Furientis has meaning. 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: Must be a U.S. Person and eligible to obtain a U.S. SECRET security clearance. Active clearance is not required at hire; we will sponsor. 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. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. 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: Company Overview: Vividion is a next generation biotechnology company based in San Diego that is leveraging its proprietary chemical proteomics platform to conduct proteome-wide foot printing of drug-protein interactions with unprecedented breadth and precision. Our technology allows us to screen, identify and optimize novel drugs that selectively bind virtually any protein, including proteins previously considered “undruggable”. Our pipeline and emerging programs reflect a matured and productive platform capable of delivering first in class drugs utilizing novel mechanisms of action (allosteric inhibitors, protein-protein interaction inhibitors, functional activators, degraders etc.) against undruggable targets in the oncology and immunology space. We prize scientific excellence, creativity, team players and we are committed to continued innovation. We have worked hard to create a collaborative and dynamic work culture where your ideas and discoveries are valued and will have an impact. We are growing and there are opportunities for mentorship and career progression. Vividion has been recognized as a Top Workplace by The San Diego Union-Tribune from 2022 to 2025. Job Summary: We are currently seeking a Scientist I level Computational Chemist to join our fast-paced computational chemistry department. This role will be responsible for supporting drug discovery efforts across several programs at various lead optimization stages by applying structure and ligand-based CADD methods. By working closely with medicinal chemists to design new analogs for subsequent synthesis, this scientist will intellectually contribute to multiple programs to advance chemical matter across various protein targets. A successful candidate will become an essential member of the drug discovery team at Vividion. Applying their expert knowledge, they will provide insights to guide the design of new drugs and creatively implement computational methods to improve the efficacy of drug design. They will be able to balance a diverse number of projects adjusting priories based on strategic need. Requirements: Essential Duties and Responsibilities: • Work as an integrated member of project teams providing computational chemistry support., • Apply cutting-edge structure and ligand based CADD methods to identify and evaluate novel chemical matter with medical chemists., • Keep current in CADD methods while integrating and developing new approaches based on the project's needs., • Work with IT to maintain and expand computing resources., • Report and present work to project teams and the broader company, including education on computational methods. Educational and Experience Requirements: • Ph.D. in computational chemistry or related field, • Industrial drug discovery experience and/or post-doctoral preferred, • A strong understanding of medical chemistry/SAR, structural biology, and biochemistry, • Expertise in commercial molecular modeling software (Schrodinger Suite (Highly Preferred), CCG, OpenEye, etc.), • Experience with a diversity of computational methods, including but not limited to docking, MD, free energy of binding methods (highly desired), homology modeling, QSAR modeling, pharmacophore modeling, QM methods, and chemoinformatics, • Experience programming or scripting (Python experience preferred), • Due to the nature of the work, a candidate with a strong understanding of biology is desirable. Required Key Attributes: • Effective troubleshooting and problem-solving skills, • Excellent computational skills, • Excellent oral and written communication skills, • Be an effective team player and strong individual contributor, flexible, and able to handle multiple tasks and deliver high quality results under tight timelines Pay & Benefits: The anticipated base salary for this position ranges from $120,000 to $135,000 depending on relevant skills, competencies, experience, and education. In addition, this position is eligible for target bonus, long-term-incentives, 401k retirement savings plan with company match, and a comprehensive benefits package which includes medical, dental, vision, life, and disability insurance. EEO & Employment Eligibility: Vividion Therapeutics, Inc. is an equal opportunity employer. All applicants will receive consideration for employment without regard to disability or veteran status. Privacy Policy: The protection of your personal information is a commitment we take seriously. For information regarding our Privacy Policy (CA candidates) please visit https://vividion.com/privacy-notice/.

Job DescriptionEnvironmental Laboratory Organic Chemist – Metals National City, CA | Full-Time Analyze with precision. Protect the environment. Build a meaningful career in science. Our client is seeking a skilled Environmental Laboratory Inorganic Chemist with experience in testing for Metals to join our team in National City, CA. In this role, you'll work with advanced instrumentation and proven EPA methodologies to analyze environmental samples that directly impact public health, safety, and environmental protection. If you're detail-driven, scientifically curious, and ready to work in a fast-paced laboratory environment, this is your opportunity to make your expertise matter. What You'll Do • Perform and/or supervise physical and chemical testing of environmental samples, • Operate ICP, Mercury Analyzers, and other advanced laboratory instrumentation, • Conduct sample preparation, digestion, and extraction using EPA methods (8270, 8260, 8081, 8082, 8015, and others), • Review and validate analytical data to ensure compliance with method and QA/QC standards, • Maintain legally defensible documentation and chain of custody records, • Receive and log samples, generate reports, and manage laboratory inventory, • Work within federal, state, and internal quality assurance programs, • Support audit readiness (AIHA/ELAP familiarity a plus) What You Bring Required Qualifications • Bachelor's degree in Chemistry or related science, • Minimum 24 semester hours of college chemistry (official transcripts required), • At least 2 years of relevant laboratory experience, • Hands-on experience with ICP and/or Mercury Analyzers, • Experience with LIMS systems, sample receipt, and analysis Core Skills • Strong attention to detail and commitment to data accuracy, • Critical thinking and problem-solving abilities, • Ability to work independently and manage priorities, • Effective written and verbal communication skills, • Proficiency in Microsoft Office Why Join Us, • Work on impactful environmental projects with real-world significance, • Gain experience with industry-standard methods and advanced instrumentation, • Be part of a long-standing, reputable laboratory network, • Collaborative team environment with opportunities to grow your expertise Additional Details, • Location: National City, CA (on-site role), • Work Environment: Laboratory setting with standard safety protocols If you're ready to apply your chemistry expertise to meaningful environmental work and grow within a respected laboratory organization, we'd love to hear from you.

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 DescriptionTitle: Associate Process Group Chemist Location: Carlsbad CA 92008 Duration: 9 Months Summary of Position: The Associate Process Group Chemist, in accordance with forecasted requirements, participates in the manufacture of products within QSR and ISO regulations. This position reviews and reconciles documents and work orders, supports assigned projects with supervision, participates in product transfers, supports departmental troubleshooting and process improvement teams, and displays an improving working knowledge of business processes as they relate to manufacturing. Essential Functions: • Manufactures (i.e. Formulates bulks, and Quality Controls) products (i.e. Lateral flow devices, controls/calibrators and microtiter systems) while adhering to regulatory requirements and business polices/procedures and schedules, • Supports departmental troubleshooting and process improvement teams, • Supports cross-functional projects and training., • Reviews completed Device History Records, performs financial review of work orders, and reports on variances to supervisor, • Maintains daily adherence to Production goals relating to MUV/LUV, labor utilization, work order closure, and schedule adherence Interactions: • Associate Process Group Chemist may have interaction with the following groups/systems. Typically with supervision:, • Inventory Control – obtains/returns materials, resolve material variances related to work order usage LN- reconciles work orders, enters/checks labor hours, checks material availability, BOMs, general manufacturing queries, and closes work orders; prepares work order variance reports., • Process Engineering - technical troubleshooting, product transfers, • Production coordinates optimization/matrix assembly, • Planning - reports on schedule adherence, • Quality/Documentation - ECO's, NCMR's, deviations, validations, QTP's Work Environment: The work environment characteristics are representative of a laboratory environment and include handling of viral and bacterial hazards, potentially hazardous chemicals, as well as infectious or potentially infectious bodily fluids, tissues and samples. Flexible work hours to meet project deadlines. Physical Demands: Position requires ability to lift up to 20 lbs. on a regular basis. Up to 75% of time at lab bench or desk, walking, standing, and sitting for long periods of time are routine to accomplish tasks in this role. Specific vision abilities required by this job include close and distance vision and the ability to adjust focus. Must have the ability to operate lab equipment. Position requires use of Personal Protective Equipment as posted. Education, Skills & Experience: • B.S./B.A. Life/Applied Sciences or equivalent experience, • Preferred minimum of 6 months of related work experience in a GMP environment Knowledge/Skills: • Basic algebraic, statistical and mathematical skills, • General computer knowledge, • Good organizational skills, • Laboratory skills, such as protein purification, antibody conjugation, solution preparation, • ELISA experience, assay development skills, etc., • Good verbal and written communication skills, • Good interpersonal skills, • Knowledge of QSR's and ISO 9001, • Knowledge of experimental design, • Basic Chemistry or Biochemistry #TB_PH #ZR Why TalentBurst? At TalentBurst, we deliver more than talent, we deliver outcomes. We partner with you to move quickly and connect you to opportunities aligned with your skills and long term growth. Backed by precision, transparency, and results, we connect top talent with leading organizations through trusted partnerships. We offer competitive compensation and comprehensive benefits, including medical, dental, vision, and retirement options. TalentBurst is an equal opportunity employer committed to an inclusive and diverse workforce. Company DescriptionFounded in 2002 by three former Monster.com executives; TalentBurst is an award-winning full-service Staffing Firm working directly with Fortune 500 companies in the US and Canada. We specialize in Contract and Contract to Permanent roles across many industries and have direct/contractual relationships with all our clients. Please visit our website www.talentburst.com or come meet us at our offices in Natick, MA, Miami, FL, Christiansburg, VA, Vineland, NJ, Houston, TX & downtown San Francisco, CAFounded in 2002 by three former Monster.com executives; TalentBurst is an award-winning full-service Staffing Firm working directly with Fortune 500 companies in the US and Canada. We specialize in Contract and Contract to Permanent roles across many industries and have direct/contractual relationships with all our clients. Please visit our website www.talentburst.com or come meet us at our offices in Natick, MA, Miami, FL, Christiansburg, VA, Vineland, NJ, Houston, TX & downtown San Francisco, CA

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, Keys Soulcare, a groundbreaking lifestyle beauty brand created with Alicia Keys, 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 28 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. 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 Description About Us We are a world-class manufacturer of high-performance silicone and EPDM hose products serving the heavy-duty truck, bus, coach, marine, military, construction equipment, and industrial markets. Based in Corona, CA, we formulate and mix our own elastomers in-house and operate across the full manufacturing spectrum, from macromolecular chemistry and fabric braiding to molding, extrusion, and final assembly. ISO 9001 and ISO 14001 certified, we are known for engineering autonomy, precision quality, and a culture of continuous innovation. Position Summary We are looking for a technically sharp and hands-on Chemist to join our team in Corona. This role sits at the intersection of formulation chemistry, quality control, and process support. You will work closely with engineering, production, and R&D to ensure our elastomer compounds meet strict performance and quality standards while contributing to ongoing product development and improvement initiatives. Key Responsibilities • Formulate, mix, and evaluate silicone and EPDM elastomer compounds for production and development purposes, • Conduct lab testing on raw materials, in-process samples, and finished products to verify compliance with internal and customer specifications, • Develop, document, and maintain Standard Operating Procedures (SOPs) and testing protocols, • Troubleshoot formulation and processing issues on the production floor and recommend corrective actions, • Support new product development by conducting literature research, running trials, and documenting results, • Collaborate with quality assurance to ensure compliance with ISO standards and customer requirements, • Track and report test data accurately using lab management or ERP systems, • Assist in managing chemical inventory, safety data sheets, and regulatory compliance documentation, • Maintain a safe, organized laboratory environment in accordance with OSHA and company safety standards Qualifications • Bachelor's degree in Chemistry, Polymer Science, Chemical Engineering, or a related field required; Master's degree a plus, • 2+ years of experience in polymer chemistry, elastomer compounding, rubber chemistry, or a related manufacturing environment preferred, • Familiarity with silicone or EPDM materials is a strong advantage, • Experience with analytical instruments such as rheometers, tensile testers, hardness testers, and FTIR, • Solid understanding of quality control methodologies and documentation practices, • Strong attention to detail with the ability to manage multiple priorities in a fast-paced production environment, • Proficiency in Microsoft Office; experience with ERP or LIMS systems is a plus, • Bilingual English/Spanish is a plus Compensation & Benefits • Salary: $65,000 - $90,000 per year, depending on experience, • Medical, dental, and vision insurance, • 401(k) with company match, • Paid time off and holidays, • Opportunities for advancement within a growing, vertically integrated manufacturing operation

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 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 DescriptionBenefits: • Life Insurance, • LTD, • 401(k), • 401(k) matching, • Dental insurance, • Health insurance, • Paid time off, • Vision insurance The 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 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 DescriptionCompany Description Eurofins Scientific is a network of independent companies providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. With over 50 laboratories and more than 40 service centers nationwide, Eurofins Environment Testing provides full-service environmental analysis across all 50 states. Our network supports public and private clients—including DoD, DOE, and municipalities—through robust logistics and continuous investment in people, technology, and infrastructure. We offer comprehensive testing for air, water, soil, sediment, tissue, and waste, covering a wide range of analytes including PFAS, metals, VOCs/SVOCs, dioxins/furans, radiochemicals, and more. Job Description Eurofins Environment Testing Southwest, Calscience in Tustin CA is searching for a VOA GC Chemist I to prepare and analyze environmental samples following EPA protocols in adherence with Eurofins Quality Assurance programs and SOP’s. Analyst duties will include, but are not limited to, the following: • Prepare water and soil samples for analysis by Purge and Trap Gas Chromatography, • Evaluate chromatography for qualitative and quantitative criteria, • Monitor and manage backlog workload to meet client program requirements, • Upload and peer review data using the laboratory information management system (LIMS), • Perform basic instrument maintenance and repair, including column replacement and ion source cleaning, • Prepare standards and reagents for sample analysis, • Maintain instrument calibrations in accordance with laboratory QAQC requirements., • Perform general housekeeping within the laboratory to maintain an organized and safe working environment, • Conduct daily duties in an efficient and safe manner, remaining compliant with environmental health and safety programs, • Performing other laboratory duties as assignedQualifications The ideal candidate would possess the following qualifications • Operating a GC in an academic or production laboratory setting is a plus., • BS or BA in chemistry or related field; 3 years laboratory experience may substitute for a degree, • Previous production oriented work experience a plus (awareness and ability to efficiently meet deadlines), • Effective time management and multitasking skills, • Ability to perform and evaluate basic mathematical calculations and formulas, • Ability to work independently following written and verbal instructions, • Strong written and verbal communication skills, • Authorization to work in the United States indefinitely without restriction or sponsorship, • Professional working proficiency in English is a requirement, including the ability to read, write and speak in English Additional Information Compensation Range: $18 - $22 per hour depending on qualifications and experience. Position is full-time. Shift available is Tuesday - Saturday, 1PM - 10PM with overtime as needed. Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base compensation may vary based upon, but not limited to, relevant experience and skill set, base compensation of internal peers, business sector, and geographic location. As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! At Eurofins, we believe sustainability is at the heart of everything we do. Guided by our vision to be the Global Leader in “Testing for Life,” our mission to contribute to a healthier and safer world, and our core values, we are building a strong foundation for Environmental, Social, and Governance (ESG) initiatives. Eurofins’ commitment to sustainability begins within our own companies through a shared responsibility to people and the planet. With climate change posing an imminent threat, Eurofins and its many companies recognize their duty to proactively reduce or offset the environmental impact of essential operations while also helping our clients do the same—serving as a true ESG Enabler. Find out more in our career page: https://careers.eurofins.com/ Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 62,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2025, Eurofins generated total revenues of EUR 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Job Description We’re Dimension . We’re doing trash differently. We’re a diverse group, who are united by a shared set of values and goals. We’re committed to performing well as individuals and in teams for the betterment of our company. Dimension is a sustainability technology company in San Francisco. We provide nation-wide B2B waste management services to America’s best companies, including Instacart, Amazon, Weee!, Sares Regis, Ashley Homestore, Restoration Hardware, Sunnova, Kiewit, and many more, and we have served many public sector customers such as DEA, DOJ, OES, and various state and local governments across the United States. Dimension is backed by notable institutions including Altair Capital, Primavera Capital, Lightspeed Ventures, Moderne Ventures, and 500 Startups. Dimension is looking for the company's first Environmental Field Chemist to join our team in San Francisco, CA. You will have a predictable, not too demanding schedule to work across customer sites in the Bay Area and beyond, assisting with packing customer waste materials in customers' facilities and at other collection sites. As the Environmental Field Chemist, you will be: • TLDR for this role: You will accompany our driver and stop by a few customer locations in California weekly on Fridays to pack hazardous waste at customer sites, preparing them for pick-up the following week. This is a once-a-week position that will require some traveling around the Bay Area., • This is a customer-facing role; you will be expected to treat customers in a friendly and professional manner. You will sometimes be expected to answer some questions as they come up., • Conducting a safe and organized work zone at each job site, • Properly document each packing job and ensure each pack has the correct labels and inventory., • Completing and filing all logs and required government paperwork in a precise and timely manner, • Responsibilities may include light warehouse work, including loading and unloading of materials onto or off of trucks or into the warehouse as assigned Required Skills & Experience • Available every Friday and able to work long hours that day. A typical day might begin at 8 AM in South San Francisco, and end at 6 pm. We will pay you based on the actual hours worked., • Perform physical functions per job requirements, • Some previous experience packing hazmat items is required., • Fluent English speaker., • US Citizen or Green Card holder, ony. Compensation + Perks • Competitive market rate hourly pay, • $25-35/hr. Based on experience & qualifications. Company DescriptionWe’re Dimension . We’re doing trash differently. We’re a diverse group, who are united by a shared set of values and goals. We’re committed to performing well as individuals and in teams for the betterment of our company. Dimension is a sustainability technology company in San Francisco. We provide nation-wide B2B waste management services to America’s best companies, including Instacart, Amazon, Weee!, Sares Regis, Ashley Homestore, Restoration Hardware, Sunnova, Kiewit, and many more, and we have served many public sector customers such as DEA, DOJ, OES, and various state and local governments across the United States. Dimension is backed by notable institutions including Altair Capital, Primavera Capital, Lightspeed Ventures, Moderne Ventures, and 500 Startups.We’re Dimension . We’re doing trash differently. We’re a diverse group, who are united by a shared set of values and goals. We’re committed to performing well as individuals and in teams for the betterment of our company.\n\nDimension is a sustainability technology company in San Francisco. We provide nation-wide B2B waste management services to America’s best companies, including Instacart, Amazon, Weee!, Sares Regis, Ashley Homestore, Restoration Hardware, Sunnova, Kiewit, and many more, and we have served many public sector customers such as DEA, DOJ, OES, and various state and local governments across the United States. Dimension is backed by notable institutions including Altair Capital, Primavera Capital, Lightspeed Ventures, Moderne Ventures, and 500 Startups.

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.

About Mercor’s talent network Join our Chemist Expert Network to connect with leading AI labs and companies seeking your expertise. About Mercor projects Experts in our network contribute to: - Training and evaluating AI models in Chemistry - Creating tasks and deliverables based on real-world

If you have a passion for aerospace and chemistry this is the role for you! Why join us? Paid for Employee Health Benefits Vacation Holiday Generous Bonus Progam Job Details Job Details: We are in search of a highly skilled and experienced Rubber Chemist to join our dynamic engineering team. Respons

Michelson Laboratories is a leading food testing laboratory based in Southern California. Since 1970, Michelson Laboratories has provided efficient testing and analyses to an extensive spectrum of customers. We have a broad-based background and are thoroughly proficient in a diverse range of industries. Our Chemistry Laboratory provides a wide range of services and is staffed with industry leading chemists. We are expanding our Chemistry department in our Commerce location and are looking for a Food Chemist. The Chemist will be responsible for performing analytical testing of food products. Responsibilities for Food Chemist: ·Review and approve data for Nutritional Labeling requests for various food products Perform titrations, extractions and analyze data for antibiotic residues, carcinogens, and other harmful chemical compounds -Troubleshoot and operate analytical instruments such as LC/MS/MS, HPLC, GC-MS, ICP-MS, ICP-OES, etc. -Troubleshoot or implement new test methods, ensure overall compliance to all regulatory and QA/QC requirements -Act as technical resource to other analysts within the department and to our clients -Prepare and review data packages/reports for reporting -Assist with special projects, method development and optimization -Review and update Standard Operating Procedures as needed. · Preparation of chemical reagents, standards, and samples for analysis · Maintaining detailed records of testing, quality activities, and chemical preparations · Ensure all analyses meet the turnaround time · Other duties as needed Qualifications for Analytical Chemist: · Master's Degree in Food Science, Analytical Chemistry, or other related sciences required. · Excellent interpersonal, verbal and written communication skills · Comfortable in a fast-paced environment with minimal direction and able to adjust workload based upon changing priorities · Ability to organize, prioritize and direct work activities; attention to detail · Time Management - ability to achieve results within expected time periods This Food Chemist position is a full-time position. Must have a flexible schedule and be available to work weekends, holidays and overtime as needed. Michelson Laboratories, Inc. is an Equal Opportunity Employer that does not discriminate on the basis of actual or perceived race, color, national origin, ancestry, sex, gender, gender identity, gender expression, pregnancy, age, veteran status, or any other legally protected status. Our management team is dedicated to this policy with respect to recruitment, hiring, placement, promotion, transfer, training, compensation, benefits, employee activities and general treatment during employment Job Type: Full-time Benefits: • 401(k), • Dental insurance, • Health insurance, • Paid time off, • Vision insurance Work Location: In person

Process Chemist – Peptide / API Manufacturing LA County California (On-Site) $70/hour 6-Month Contract-to-Permanent Opportunity A leading peptide manufacturing organization is seeking a Process Development Scientist to support the advancement of innovative API processes from early development through full-scale cGMP manufacturing. This is a hands-on opportunity to work at the intersection of chemistry, process development, and commercial manufacturing supporting next-generation peptide and oligonucleotide medicines. The ideal candidate will bring strong synthetic chemistry expertise, process optimization experience, and the ability to collaborate cross-functionally in a fast-paced GMP manufacturing environment. Key Responsibilities • Develop, optimize, and scale synthetic processes for peptide and oligonucleotide APIs from lab through manufacturing, • Support technology transfer activities from Process Development into Production across internal sites, • Monitor and optimize chemical reactions, purification operations, isolation, and drying processes, • Perform and interpret analytical testing including High-performance liquid chromatography purification, in-process sampling, and related process analytics, • Troubleshoot process, equipment, and manufacturing challenges to improve efficiency and yield, • Partner closely with Production, QA, QC, Engineering, and Supply Chain teams to ensure compliant execution, • Author and review batch records, protocols, reports, SOPs, and technical documentation, • Drive continuous improvement initiatives focused on safety, right-first-time execution, and scalable manufacturing readiness Qualifications • PhD in Chemistry, Chemical Engineering, Organic Chemistry, or related discipline with 1+ year industry experience, • OR, • Master’s degree with 5+ years relevant industry experience, • Minimum 4+ years of industry experience in organic chemistry, process chemistry, or API development, • Experience with peptide chemistry, peptide manufacturing, or complex molecule synthesis strongly preferred, • Strong understanding of synthetic route development, scale-up, and process optimization, • Familiarity with cGMP environments, deviation management, and technical documentation, • Hands-on experience with analytical techniques such as High-performance liquid chromatography, UPLC, and reaction monitoring tools preferred, • Excellent troubleshooting, communication, and independent problem-solving skills Preferred Experience • Solid Phase Peptide Synthesis (SPPS), • Oligonucleotide API manufacturing, • Tech transfer between R&D and commercial manufacturing, • Purification, filtration, lyophilization, and drying operations, • Working in multi-site manufacturing environments Why Join • Contract-to-hire opportunity with long-term growth potential, • Work with a recognized leader in peptide manufacturing, • Direct impact on therapies advancing modern medicine, • Strong exposure to development through commercial-scale production

California Clinical Chemist Scientist License - CA Department of Public Health; California Clinical Cytogeneticist Scientist License - CA Department of Public Health; California Clinical Genetic Molecular Biologist Scientist License - CA Department of Public Health; California Clinical Histocompatab