Chemist jobs in California

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.

Job Description About us: Valent U.S.A. LLC, a wholly owned subsidiary of Sumitomo Chemical Company, Limited, engages in the development, registration, sales, and marketing of integrated technological solutions for crop production and pest management that deliver value for our customers and stakeholders. A leading crop protection firm serving the agricultural and non-crop products markets in North America, Valent products help growers produce safe and abundant food and fiber crops, and horticultural professionals improve the quality of life for their customers. The corporate motto, Products That Work, From People Who Care®, describes the company's business philosophy. Valent seeks out and provides customers with innovative and effective solutions to their production challenges. Our vision is to be the best company delivering integrated solutions of biorational and traditional crop protection solutions to our customers. Valent is dedicated to creating a world that is healthier and more comfortable, and that has a sustainable abundance of quality, affordable food, helping crops to be the ultimate renewable resource. General Description: The purpose of this position is to direct the activities of a scientific group in the research and/or development of an organization's products, projects, and programs. Conducts and collaborates with others on basic research and development relevant to long-term objectives and concerns. Writes and reviews documents for submission to federal (EPA) and state regulators. Develops strategies to ensure effective achievement of scientific objectives. Monitors and evaluates completion of tasks and projects. May develop budgets for capital expenditures and labor. Typically participates with other top managers to establish company policies. Makes final decision on administrative or operational matters. Principal Responsibilities: • Serve as Study Director with overall responsibility for insuring that assigned studies are conducted in compliance with regulatory Good Laboratory Practice and FIFRA guidelines. Monitor and be accountable for validity of contracted studies. Prepare protocols and reports with scientifically valid conclusions for submission to government agencies. Prepare responses to technical issues from regulatory agencies on submitted studies., • Plan, direct, and execute laboratory research projects with responsibility for data quality and timeliness of completion. Exercise judgment in selecting methods from generally defined practices and techniques and evaluation criteria for obtaining results. Utilize technical expertise to overcome technical challenges by innovatively developing/modifying methodology to generate scientifically valid data. Develop solutions to complex technical problems., • Maintain timelines for completion of multiple projects by management of manpower/equipment resources and effective project scheduling. Provide management with realistic time, manpower, and cost estimates for proposed projects. Communicate effectively with internal customers and multi-discipline team members on project status., • Expand and maintain knowledge in area of expertise and regulatory guidelines. Serve as a resource for peers, Associate Scientists, and project managers. Train less experienced colleagues in application of new/revised methodologies, and in laboratory and instrumental techniques. Evaluate technical advances in field and their potential application to research efforts., • Serve as a member of multi-discipline project team or technical task forces, providing input for strategic planning to meet regulatory objectives., • Evaluate technical advances in field and potential application to research efforts. Serve as a resource for colleagues, Associate Chemists, R&RA project managers, and other internal functional areas. Provide input for strategic planning to meet regulatory objectives., • Supervise Chemists and Associate Chemists; assign tasks/projects; train and develop; communicate priorities and objectives; conduct performance reviews. Mentor and develop others using time management and performance development tools. Serve as a resource for other members of the group. Follow safety and regulatory plans, and waste disposal procedures. Participate in all required safety meetings and training programs., • Perform research and/or development in collaboration with others for projects. Provide technical expertise in the design, execution, and interpretation of experiments that contribute to project strategies. Make detailed observations, analyze data, and interpret results for technical reports and summaries., • Typically, a MS, PhD or equivalent, with 9 – 12 years of related experience, plus 5 – 7 years of management experience., • Strong interpersonal management skills; exceptional time management, negotiation, and organizational skills., • Strong interpersonal management skills; exceptional time management, negotiation, and organizational skills., • Detail-oriented evaluation and interpretation of data., • Maintenance & trouble shooting of analytical equipment. Problem solving and method development skills., • In-depth knowledge of chromatography theory & application techniques - including purification techniques, use of liquid and gas chromatographs, and use of selective detectors and mass selective detectors. Knowledge of environmental fate, metabolism, and residue methodology., • In-depth knowledge of USEPA/FIFRA Guidelines & Good Laboratory Practice guidelines, including study design and protocol development. Physical Demands and Work Environment (FIELD Position) The physical demands and work environment characteristics described below are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. • Physical Demands include constant walking, standing, bending at the neck and waist, squatting, climbing, kneeling, crawling, twisting at the neck and waist, simple grasping, power grasping, and fine manipulation with hands, pushing and pulling with hands, reaching above shoulder level, and lifting and carrying up to 50 lbs.; also frequent lifting and carrying of up to 75 lbs., occasional sitting and lifting and carrying of up to 100+ lbs. Travel by air or car up to 50% of the time and will be required to drive safely for long distances., • Work Environment includes exposure to or working in or around moving cars, trucks, forklifts, equipment, and machinery including a computer keyboard and mouse; uneven ground; excessive noise; extremes in temperature, humidity, or wetness; dust, gas, fumes, or chemicals; venomous insects and animals, heights; operation of foot controls or repetitive foot movement; use of special visual or auditory protective equipment. May be required to work outdoors in an agricultural crop field, assist in putting out demonstration plots, wear respirator and other personal protection equipment., • Frequency Definitions: Constant = Over 40% / Frequent = Up to 40% / Occasional = Up to 10% What We Offer: You’ll enjoy competitive compensation, consisting of base pay plus an incentive program available to all eligible full-time employees, and a comprehensive benefits package including high-quality healthcare options, 401k matching, life and disability insurance, generous time off (with time off to volunteer) and much more! Additionally, we offer several Flexible Work Arrangements to support a healthy work-life balance. We work together to power our sustainable future. Here's what drives us: Valent U.S.A. LLC has a strong commitment to both sustainability and corporate social responsibility (CSR). In fact, being a responsible corporate citizen has been ingrained in our culture since the company’s founding. Today, it remains at the forefront of everything we do. • Valent U.S.A. LLC is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation and/or identity, national origin, citizenship, immigration status, disabilities, or protected veteran status. #LI-ONSITE

UC Davis Screening Chemist Salary or Pay Range: $30.32 - $48.78/hour (Department budgeted salary range: $34.14/hr. Commensurate with experience.) Under direction of the Lab Research Supervisor 2, responsible for the performance of organic analysis for the determination of drugs and their metabolites in biological specimens using liquid chromatography - mass spectrometry and other analytical techniques. Responsible for care and maintenance of laboratory equipment and complex analytical instruments. Responsible for participating in the update and development of analytical procedures, quality control procedures, and Standard Operating Procedures (SOPs). Qualifications Minimum Qualifications - For full consideration, applicants are encouraged to upload license and/or certification if required of the position • Experience in sample preparation techniques such as solid phase and liquid-liquid sample extraction, sample fortification and matrix matching and skills to prepare analytical reagents, solutions, controls and standards. • Skills operating a wide range of manual and computer-controlled analytical equipment including Gas Chromatograph, Liquid Chromatograph and Mass Spectrometers, including maintenance and trouble-shooting of equipment to obtain maximum performance from instruments. • Skills in the operation and maintenance of a wide range of laboratory equipment used in sample preparation including mircoliter pipettes, pH meter, sonicator, evaporator, centrifuge, analytical balance, automated SPE instruments, and analytical instruments. • Skills to perform mathematical calculations, and knowledge of statistical analysis. • Familiarity with literature sources of analytical procedures with organizational skills to schedule work activities. • Knowledge of and skills to follow safe working practices including handling/disposing of hazardous materials. Preferred Qualifications • BS degree in analytical chemistry or a related scientific discipline, and/or equivalent work experience related to performing techniques and procedures for analysis of biological samples as described in the Standard Operating Procedures in a laboratory environment. • Experience working in a high volume, high throughput analytical laboratory, in a regulated industry with knowledge of QA/QC to continuously produce high quality data. • Competency using various forms of chromatographic software such as ChemStation, Xcalibur, and/or Tracefinder software. • Ability to apply good laboratory practices as well as safety procedures and other policies and procedures outlined by CAHFS, the EACL Laboratory, and the University. Key Responsibilities • 75% - Analytical Procedure & Testing • 10% - Quality Control • 10% - Laboratory Management • 5% - Method Development and Project Assistance Special Requirements – Please contact your recruiter with questions regarding which activities apply by position • This is a critical position, as defined by UC Policy and local procedures, and as such, employment is contingent upon clearing a criminal background check(s) and may include drug screening, medical evaluation clearance and functional capacity assessment To view full job description and submit an on-line application, visit UC Davis Career Opportunities at: Job ID#: 82498 The University of California, Davis is an Affirmative Action/Equal Opportunity Employer

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

Growing innovative Food & Beverage manufacturer is experiencing significant growth, and with that comes exciting opportunities. We’re seeking a Senior R&D Food Chemist to join our dynamic team. Title: Senior R&D Food Chemist Pay rate range: $35-45/hr Location: San Fernando Valley, CA 3-month, contract-to-hire role Role Overview: The Senior Chemist will be responsible for the development, enhancement, and matching of products using both existing and new raw materials. This includes calculating product costs, creating master formulas, and overseeing prototype evaluations. The role may also involve supervising and mentoring other chemists and lab technicians. Key Responsibilities: • Independently develop innovative product based on customer and internal requirements, • Match competitor products and improve existing formulations, • Evaluate project feasibility in terms of production, technology, and cost, • Perform cost analysis and propose pricing for developed products, • Develop and maintain product formulas and specifications, • Collaborate directly with customers and provide technical support, including on-site assistance during first-time production runs, • Provide training and support to junior chemists and lab technicians, • Assist in organizing sample guidelines and policies, • Serve as R&D point of contact in the manager's absence, • Support Quality Control and Production teams during initial production processes, • Perform additional duties and special projects as needed Qualifications: • Bachelor's degree in Chemistry, Food Science, or a related discipline, • Minimum of 4 years of relevant experience in a R&D bench role., • Proven expertise in R&D and laboratory work, • Strong analytical and problem-solving skills, • Effective communication and teamwork abilities

Job Description Job Description: * This position is accountable for performing clinical laboratory testing, following all applicable policies and procedures * Independently performs moderate to highly complex clinical tests following the required procedures and policies. * Performs newly introduced tests to the laboratory that require defined skills. * Prepares and oversees the preparation of reagents or media as well as stock solutions, standards, and controls. * Tests new reagents or controls and evaluates their usefulness based on standard criteria. * Determines the acceptability of specimens for testing according to established criteria in testing procedures. * Determines calculated results utilizing testing data by means of manual or computerized procedures. * Accurately enters results of testing. * Checks the computer review reports to monitor accurate reporting of laboratory results. * Adheres to analytical schedules to maintain turnaround times of results. * Evaluates the acceptability of routine and complex analyses prior to releasing patient reports. * Recognizes and takes appropriate action in response to critical values or unusual or unexpected results, and documents action taken. * Responsible for preventative maintenance, troubleshooting and calibration of laboratory equipment. * Evaluates the results of instrument performance checks. * Performs linearity, accuracy and precision checks as required. * Performs Quality Control and calibrations with the appropriate frequency and evaluates results, to determine acceptability of result release. * Selects and evaluates control materials using established criteria. * Initiates a corrective action process whenever test systems do not perform according to the established criteria. * Accurately performs and records proficiency testing. * Demonstrates the ability to detect and correct technical and operational problems. * Notifies the supervisor, and contacts manufacturer or field service support for additional assistance, if necessary. * Ensures accurate tracking and labeling of reagents and supplies. * Consistently maintains a safe and neat work area. * Demonstrates effective two-way communication with staff, immediate manager, suppliers, internal and external customers, via meetings, written and verbal interactions, to create an informed positive environment. * Actively participates in staff meetings, and in Quality Improvement meetings as assigned. * Takes on additional business-related responsibilities or projects, as delegated by the Supervisor or Manager. * This may include but not be limited to evaluation of new techniques and procedures in terms of personnel and requirements, method comparison, cost analysis, establishment of reference ranges, writing and revising technical procedures, and evaluation of productivity and key results measures. * Responsible for following all required procedures, practices and related guidelines as provided in company policy and associated procedures for safety, environmental, and infection control. * Collects and dispose of waste in proper receptacles. * Demonstrates a high level of integrity and honesty in maintaining confidentiality. * Provides direct and constant supervision to unlicensed staff as necessary and trains staff in proper performance of both routine and complex procedures. * Supports Training Programs, where applicable. * Maintains professional growth and development through continuing education. * The continuing education must meet the education requirements for California state licensure. * Answers phones, transfers, or takes accurate messages. * Complies with all health and safety policies, procedures, and practices. * Required to use personal protective equipment. Qualifications: * California CLS license (Generalist or Chemist) * BS in medical technology or other life/physical sciences from an accredited college or university is REQUIRED * Zero to three year's direct experience in a laboratory setting * Physical and Mental Requirements: * The normal performance of duties may require lifting and carrying objects. Objects in the weight range of 1 to 10 pounds are lifted and carried frequently; objects in the weight range of 11 to 25 pounds are lifted and carried occasionally and objects in the weight range of 26 to 50 pounds are seldom lifted and carried. * Objects exceeding 50 pounds are not to be lifted or carried without assistance. * Ability to perform repetitive tasks. * Frequent simple grasping, reaching and fine manipulation. * Ability to sit and/or stand for long periods. * Have good eye and hand coordination. * Testing for color blindness will be required upon hiring or transfer into technical functions requiring detection of, or rating of intensity of colors (e.g., Fluorescent microscopy reading). * Proficiency in Microsoft Office Application (Word, Excel, Outlook) * Strong typing skills desirable. * Other automation skills helpful. * Shift/Time Zone: 8 pm - 4 am PST California Fair Chance Act: Synectics Inc. will consider qualified applicants with a criminal history pursuant to the California Fair Chance Act. You do not need to disclose your criminal history or participate in a background check until a conditional job offer is made to you. After making a conditional offer and running a background check, if Synectics Inc. is concerned about conviction that is directly related to the job, you will be given the chance to explain the circumstances surrounding the conviction, provide mitigating evidence, or challenge the accuracy of the background report. Find out more about the Fair Chance Act by visiting calcivilrights.ca.gov/fair-chance-act/. Benefits: Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st. Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification. Synectics is an equal 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., • 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 DescriptionCompany Description LGC Genomics locations Petaluma and Novato, CA, as well as our sister site in Denmark, represent a focused, collaborative culture of producing mission-critical genomics components, primarily oligonucleotides and supporting reagents, for our diverse customer base. We believe in Science for a Safer World and have embodied our mission by supporting first responders during the COVID-19 pandemic where our Biosearch Technologies portfolio has been and continues to be enabling millions of PCR tests worldwide. We are currently seeking candidates who are up for the challenge of operating in a high-growth, purpose-driven organization. Job Description Position Summary: This role is responsible for the manufacturing of Controlled Pored Glass (CPG) materials by following established and robust protocols. This position will primarily work with solid phase chemistry that is used in oligo manufacturing. CPG material manufacturing includes amine and nucleoside modification of native CPG at various angstrom sizes as well as modification with proprietary dyes and quenchers. The Chemist I will also be responsible for the upkeep of basic CPG equipment used in these processes. Chemist Technician 1 and 2 designation is based off competency and experience level. • Perform assigned tasks using the established protocols and methods on the appropriate equipment and within the given final specifications and timeline., • Responsible for the manufacturing of robust protocols by demonstrating a working knowledge of routine tasks while supporting and collaborating with colleagues to ensure critical tasks are met., • Write and revise standard operating procedures according to LGC Quality guidelines., • Continuously replenish inventory of CPG products as assigned by Associate Supervisor., • Effectively communicate to ensure all equipment is functional and available for use and coordinate with CPG Manufacturing supervisor to ensure the most efficient use of time and resources. This includes making recommendations to supervisor as necessary regarding resources required to meet objectives and timelines., • Maintain a safe, organized, and clean workspace., • Record real time data onto physical and electronic batch records following good documentation practices., • Comply with all company, departmental, regulatory policies and rules., • Other duties as assigned.Qualifications Minimum Qualifications: • Bachelor’s Degree in a Physical Science with 0-2 years industry experience in a laboratory setting or 2-4 years of industry experience or equivalent combination of education and experience that demonstrated proficiency to meet requirements of a Chemist Technician 1 and 2., • Excellent understanding of laboratory, chemical and general safety practices in a manufacturing environment., • Capable of running multiple reactions in process at any one time to efficiently produce requested materials and submit products by expected deadlines., • Adhere to company safety PPE policy., • Strong attention to detail and time management skills., • Excellent verbal and written communication skills., • Multi-tasker, flexible and proactive., • Good computer and data entry skills including use of Microsoft Outlook, Word, Excel, and web browser(s)., • Competent with chemical calculations for molarity, density, and use of the metric system. Additional Information What we offer (US based-employees): • Competitive compensation with strong bonus program, • Comprehensive medical, dental, and vision benefits for employees and dependents, • FSA/HSA Pre-tax savings plans for health care, childcare, and elder care, • Deductible Buffer Insurance and Critical Illness Insurance, • 401(k) retirement plan with matching employer contribution, • Company-paid short- and long- term disability, life insurance, and employee assistance program, • Flexible work options, • Pet Insurance for our furry friends, • Enhanced Parental leave of 8 additional weeks, • PTO that begins immediately Chemistry Technician 1 and 2 designation is based off competency and experience level. Minimum: $ 22.35 Maximum: $37.25 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. All your information will be kept confidential according to EEO guidelines.

Job Description WHO WE ARE We are a company where people matter. We are family driven. We are financially strong. And we are looking for problem-solvers to join our growing team. BENEFITS • Competitive pay, • Professional development workshops & training, • In-person networking opportunities with leadership and peers, • Hands-on project experience with real business impact, • Paid volunteer time, • Company-sponsored events and activities QC Lab Intern (Summer 2026) The primary purpose of this position is to perform required quality control projects while providing support to Quality Control Chemists and ensuring that all Quality Assurance/Quality Control practices and procedures are followed. This position will uphold the Hydrite "Standards of Excellence" through continuous commitment to customer satisfaction, both internal and external. Primary responsibilities include: • Perform daily laboratory activities to support Quality Control Chemists., • Perform instrument maintenance, calibrations, quality control checks, solutions preparations and standardization., • Perform required quality control analysis of incoming, manufactured, and outgoing materials under the supervision of a Quality Control Chemist., • Perform administrative duties which includes the generation, distribution and filing of Certificates of Analysis., • Maintain records accurately, neatly, legibly and completely., • Maintain a clean and neat laboratory at all times., • Clean glassware., • Perform all duties outlined in relevant SOPs and all other duties to be assigned., • All staff members are responsible for reporting food safety problems to their supervisor or the SQF Practitioner upon observation of a known or potential issue., • Uphold Hydrite's Standard of Excellence through a continuous commitment to maintain quality facilities and provide quality products and services to internal and external customers., • Must be studying to obtain a degree in Chemistry (Junior or Senior)., • Completion of following core Chemistry courses: Analytical Chemistry, Physical Chemistry, Organic Chemistry, and associated labs., • Must possess good laboratory analytical skills., • Basic computer skills and knowledge of MS Office., • Able to apply advanced math skills and use involved problem solving., • Must be self-motivated., • Summer Kick-Off Event: A two-day introduction with plant tours, leadership Q&A, team-building, and networking with interns and co-ops across Hydrite., • LinkedIn: linkedin.com/company/hydrite-chemical-co-, • Facebook: facebook.com/hydrite Privacy Notice for California Residents:

Job DescriptionDescription: About GondolaBio GondolaBio is a clinical-stage biopharmaceutical company focused on developing breakthrough therapeutics for genetic diseases. GondolaBio is an independent sister company to BridgeBio, originally carved out in 2024 after securing $300M in private financing from external investors. GondolaBio aims to leverage cutting-edge biological research to discover, create, test, and deliver transformative medicines to treat patients who suffer from genetic diseases. Who You Are We are seeking an experienced and talented process chemist to lead process chemistry activities for a pre-IND small molecule. The Process Chemist will be responsible for developing, optimizing, and scaling synthetic routes for our clinical candidate. This individual will lead drug substance process development, including route scouting, lab-scale optimization, and technology transfer to CROs and CDMOs. The ideal candidate is a strong synthetic organic chemist with experience in process chemistry, scale-up, and external partner management. Requirements: Key Responsibilities • Lead process development for the company’s oral small molecule drug substance., • Design, evaluate, and optimize synthetic routes to improve yield, robustness, scalability, and sustainability., • Perform route scouting and select optimal synthetic strategies for scale-up., • Oversee process chemistry activities at CROs/CDMOs, including tech transfer, process optimization, and GMP manufacturing., • Identify and mitigate potential scale-up risks (safety, quality, regulatory)., • Collaborate cross-functionally with internal teams (CMC, formulation, regulatory, program management)., • Prepare process development reports and regulatory documentation to support IND/clinical filings., • Ph.D. in Organic Chemistry, Process Chemistry, or related discipline; M.S. with significant industry experience considered., • 5+ years of relevant experience in pharmaceutical or biotech process development., • Strong background in synthetic organic chemistry, route design, and optimization., • Demonstrated experience with drug substance scale-up and GMP manufacturing., • Proven ability to manage CROs/CDMOs and drive external partnerships effectively., • Excellent problem-solving, organizational, and communication skills., • Thrives in a fast-paced, entrepreneurial environment with a hands-on approach, • Up to 20% travel may be required., • Excellent communication skills with both technical and business stakeholders, • Patient Champions, who put patients first and uphold strict ethical standards, • Entrepreneurial Operators, who drive toward practical solutions and have an ownership mindset, • Truth Seekers, who are detailed, rational, and humble problem solvers, • Individuals Who Inspire Excellence in themselves and those around them, • Patient Days, where we are fortunate to hear directly from individuals living with the conditions we are seeking to impact throughout the year and learn how we can improve our efforts, • A culture inspired by our values: put patients first, think independently, be radically transparent, every minute counts, and let the science speak, • A place where you own the vision for your own career path, • A collaborative, fast-paced, data-driven environment where we inspire ourselves and each other to always perform at the top of our game, • Access to learning and development resources to help you get in the best professional shape of your life, • Robust and market-competitive compensation & benefits package (Base, Performance Bonus, Equity, health, welfare & retirement programs), • Flexible PTO, • Rapid career advancement for strong performers

Job DescriptionBenefits: • 401(k), • 401(k) matching, • Dental insurance, • Health insurance, • Paid time off 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 Competencies • Masters degree in Chemistry, Chemical Engineering, Biochemistry, Biomedical or related field is required, • Hands-on experience 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

Job DescriptionSalary: $80K-$100K, depending upon experience Cogent Scientific, an insourced contract research organization, is looking for the right people to accomplish our Mission: to partner in the global effort to improve lives through innovative science with an experienced workforce. We can offer you the chance to build on your skills and knowledge whileworking among experts in their fields and with cutting-edge instrumentation. Cogent Scientific offers competitive pay, attractive benefits, and an exciting work environment (as well as relocation bonus as needed). We aim to recruit the best people who stand out among their peers and embody our Core Values: Client Focused: We only succeed when our clients succeed. Outstanding: We deliver meticulous results through outstanding performance. Good: We act ethically and morally. Employee-Centric: We honor and support our employees. Nimble: We are prepared to adapt in an ever-changing industry. Team-Oriented: We collaborate with each other and with our clients. We currently have a role available for a Small Molecule Purification Chemist. Job duties include, but are not limited to: • Identifying, characterizing and purifying small molecule pharmaceutical compounds using analytical and chromatographictechniques (UPLC, HPLC, SFC, LC-MS, etc.)., • Conducting preventative maintenance and troubleshooting on instrumentation as needed., • Developing methods on LC and SFC., • Investigating LC-MS columns/methods for specific projects., • Working as a team with other chemists, external resources and data management groups. Job requirements include, but are not limited to: • MS in Biochemistry, Chemistry or related field with 5+ years of pharma laboratory experience outside of academia/academic research., • Extensive theoretical knowledge of UPLC, LC, LC-MS required, as well as hands-on experience with Waters and Agilent systems., • Excellent communication skills verbal and written., • Works well both within a team and as an individual., • Demonstration of excellent team player and collaboration skills, very strong attention to detail, very strong problem-solving skills, a high level of learning agility, and the ability to work across functions., • The ideal candidate will be enthusiastic and self-motivated, with the leadership and communication skills necessary to operate effectively in a fast-paced multidisciplinaryenvironment with flexibility and an adaptable approach to goal delivery.

Job DescriptionSalary: $120K-$150K, depending upon experience Cogent Scientific, an insourced contract research organization, is looking for the right people to accomplish our Mission: to partner in the global effort to improve lives through innovative science with an experienced workforce. We can offer you the chance to build on your skills and knowledge while working among experts in their fields and with cutting-edge instrumentation. Cogent Scientific offers competitive pay, attractive benefits, and an exciting work environment. We aim to recruit the best people who stand out among their peers and embody our Core Values: Client Focused: We only succeed when our clients succeed. Outstanding: We deliver meticulous results through outstanding performance. Good: We act ethically and morally. Employee-Centric: We honor and support our employees. Nimble: We are prepared to adapt in an ever-changing industry. Team-Oriented: We collaborate with each other and with our clients. We currently have a role available for an Expert Pharma Analytical Chemist. Job duties include, but are not limited to: • Conducting preventative maintenance and troubleshooting on instrumentation as needed., • Developing methods on LC and SFC., • Investigating LC-MS columns/methods for specific projects., • Working as a team with other chemists, external resources and data management groups. Job requirements include, but are not limited to: • Functional knowledge of NMR preferred (theory, instrument operation and maintenance, result interpretation)., • Excellent communication skills verbal and written., • Works well both within a team and as an individual.

Job Description Laboratory Technician A stable family-owned aerospace company is looking for an entry-level laboratory technician. Generous benefits package including medical, dental, life, and 40% matching 401k with no cap. Must be able to pass pre-employment physical and DOT-mandated drug test. Build a career and discover why most of our team members have been with us for 10-20 years! We are looking for career-minded individuals who want to grow with our team. Bring a positive attitude and a desire to grow and build a career. We will invest our time and energy to help you achieve your goals. Must be able to perform all lab analyses using burettes, pipettes, pH/ion meters, atomic absorption spectrophotometer, hydrogen analyzer, laboratory balance, and all other lab-related equipment. All lab analyses and special tests will be performed for reporting to the Chief Chemist, Quality Manager, and Plant Manager. You will be exposed to hazardous materials and waste while performing daily job duties. Specializing in inorganic analysis Essential Duties, Responsibilities & Requirements: · Is a good communicator. · Have a willingness to learn Physical Demands and Work Environment: An employee must meet the physical demands described here to perform the essential functions of this job successfully. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. While performing the duties of this position, the employee will be required to perform some physical exertion as necessary. Also, will regularly be required to sit, stand, walk, kneel, and occasionally bend and move about the facility. The work environment characteristics described here represent those an employee encounters while performing the essential functions of this job · The noise level in the work environment may be louder than average. Earplugs will be required when necessary · While performing the duties of this job, the employee regularly works near moving mechanical parts · While performing the duties of this job, the employee regularly works with hazardous chemicals · The building conditions can be very cold in the winter and extremely hot in the summer · The Chemical Milling areas are dirty & wet at times. Housekeeping and focus are required to avoid slip hazards. This job description is subject to change at any time. Work Schedule: 8 -hour Shifts- 5:00 am – 1:30 pm Monday - Friday Compensation: $25.00 - 28.00 Per Hr. Company DescriptionFamily-owned and operated since 1989. Lots of room to grow in a thriving business.Family-owned and operated since 1989. Lots of room to grow in a thriving business.

Job Description Frontier Medicines is seeking a highly motivated individual to fill the position of Principal Scientist, Computational Chemistry. The successful candidate will play a leading role in developing medicinal chemistry optimization strategies for key drug discovery programs. This individual will review experimental results, develop SAR hypotheses for activity, selectivity, and properties, and make design suggestions to improve the profiles of small molecule drug candidates. As a covalent drug discovery–focused company, there is the opportunity for method development within this evolving field, in addition to applying the full range of ligand-based and structure-based design approaches and leveraging data from chemoproteomics, AI and quantum mechanics. This role is key to Frontier Medicines’ success and an opportunity to work in a highly collaborative and energetic environment with short communication lines across functions and departments, and regular interactions with senior leaders. As the senior computational chemist, there is furthermore an opportunity to build out the computational team in the future Requirements What will you be doing? • Design, execute, and analyze computational chemistry studies using a wide range of ligand-based, structure-based, and physics-based modeling techniques., • Partner closely with medicinal chemists and biologists to develop and refine structure–activity relationships (SAR), optimize molecular properties, and guide design hypotheses., • Contribute to project strategy and decision-making across all discovery stages, including target assessment, hit identification, lead optimization, and development candidate nomination., • Champion innovative computational tools and workflows, identify and implement emerging technologies that enhance Frontier’s CADD capabilities – specifically with an eye to the applicability to the covalent domain., • Work closely and partner with the AI team to develop and integrate novel AI applications into daily drug design workflows, • Communicate scientific results, design rationales, and strategic insights to multidisciplinary teams and senior leadership. What are we looking for? • Ph.D. in Computational/Theoretical Chemistry, Biophysics, or a related discipline with 5+ years of relevant industry experience in drug discovery (biotech or pharma)., • Demonstrated expertise in applying computational chemistry to small molecule design and optimization., • Strong experience with leading computational chemistry tools, CCG tools including MOE is highly preferred, • Basic knowledge of scripting and programming with Python preferred, • Experience with quantum mechanics (QM) is highly preferred, • Proven track record of scientific impact, as evidenced by publications, patents, and successful project contributions., • Solid understanding of medicinal chemistry principles, SAR analysis, and ADMET optimization., • Excellent communication, presentation, and cross-functional collaboration skills., • Ability to operate independently and as a scientific leader in a fast-paced, startup environment., • Legally authorized to work in the U.S. Benefits • Health Care Plan (Medical, Dental & Vision), • Retirement Plan (401k, IRA), • Life Insurance (Basic, Voluntary & AD&D), • Paid Time Off (Vacation, Sick & Public Holidays), • Family Leave (Maternity, Paternity), • Short Term & Long Term Disability, • Training & Development, • Free Food & Snacks, • Wellness Resources, • Stock Option Plan At Frontier, we strive to build a diverse and equitable workplace. The salary range for this role is $175,000 - $231,000. Compensation for the role will depend on a number of factors, including candidates' qualifications, skills, competencies and experience. Frontier offers a competitive total rewards package which includes healthcare coverage, 401k and a broad range of other benefits. This compensation and benefits information is based on Frontier's knowledge as of the date of publication, and may be modified in the future.

Job DescriptionCompany 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 works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins 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. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description The Chemist I performs testing activities as directed by Department Manager/Supervisor in accordance with all applicable company and regulatory guidelines to ensure that quoted turnaround times are met in support of monograph testing, unknown/failure analysis and other areas. Authority The Chemist I receives sufficient authority from, and is accountable to, the Department Manager/Supervisor, or appointed designate, for the successful completion of assigned duties and responsibilities and has the authority to take action necessary to carry out the duties and responsibilities of this position and to identify the occurrence of departures from the quality system or from the procedures for performing tests and/or calibrations, so long as such action does not deviate from established company guidelines, is consistent with sound technical and business judgment, and follows the practices of the laboratory. Essential Duties and Responsibilities • Perform testing activities as directed by Department Supervisor in accordance with all applicable company and regulatory guidelines., • Monitor backlog and plan testing schedule to ensure quoted turnaround times are met., • Wet chemistry techniques utilized will include gravimetry, titrimetry, colorimetry and others as needed., • Instrumentation utilized may include HPLC, GC, ICP, ICP-MS, IC, and others as needed., • Maintain neat and accurate records., • Enter testing data into LIMS and monitor for QC failures., • Review and approve laboratory analytical data., • Monitor and record environmental conditions in laboratory. Alert management of any out of tolerance findings., • Perform calibrations/checks of laboratory equipment., • Maintain glassware inventory for laboratory use., • Maintain chemical/reagent traceability., • Assist with maintenance of chemical/supply inventory., • Support the maintenance of controlled documents related to laboratory operations/testing through editing of documents and/or reviewing revisions., • Support quality system improvements through completion of Corrective and Preventive Action forms, documenting Non-Conformances and assisting with internal audit findings as assigned by Environmental Lab Supervisor or Monograph Supervisor., • Maintain regular attendance and punctuality., • Conducts all activities in a safe and efficient manner., • Perform other duties as assigned.Qualifications, • B.S. in Chemistry or related field, • Experience with HPLC, GC, and wet chemistry techniques preferred., • Knowledge of ISO 17025, DEA, EPA, FDA and related guidance., • The role is an entry to mid level for a Chemist based in person at 2841 Dow Avenue, Suite 200, Tustin, CA 92780, • This is not your average Chemist role in a routine lab. The candidate must understand that this role is for an investigative / custom projects lab so he or she must bring a level of maturity., • The ideal candidate is: local to Southern California and is comfortable commuting to Tustin Monday-Friday, • Technical skill is important: experience in utilizing instruments such as GC-MS, HPLC, DSC, TGA, and is receptive to learning and growing technically Additional Information Compensation: • Excellent full time benefits including comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match

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 a 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., • BA/BS degree in Chemistry related field, or 1 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, • 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

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.

Job DescriptionQC Analytical Chemist- Torrance, California Rate: $32.00 to $35.00 Analyzes Raw Materials, In-Process Samples and Finished Goods Includes the following: Other duties may be assigned. • Analyzes compounds 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., • Monitor and trend QC data results, • Follows established procedures and documents all findings and results timely, concisely, clearly and accurately., • Prepares standards and specifications for processes, facilities, products, and tests., • Measures products for compliance to standards and specifications and reports same., • Provide updates/escalations at daily and weekly site-specific and cross-site meetings., • 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., • Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/ 210/ 211). Knowledge of regulatory requirements for data integrity and practices., • Knowledge of regulatory guidance and experience maintaining QC lab GMP compliance and audits, • Assessment of GMP systems currently in place to ensure compliance., • 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., • Provides input to the development of procedures., • 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, • A minimum of 3 years’ experience and BS or BA. Preferred:, • Demonstrated leadership and management skills, including establishing direction and goals, and building good work ethics for the team, • Supervising/managing experience. At Prime, we believe that a diverse, equitable and inclusive workplace makes us a more relevant, more competitive, and more resilient company. We welcome people from all backgrounds, ethnicities, cultures, and experiences. Prime is an equal opportunity employer. Powered by JazzHR 7E6szuOuXD

Job Description Job Description: Onsite POSITION SUMMARY: The Company has anopportunity in the Advanced Measurement Sciences (AMS) Analytical Group atour Research and Development Center in Pleasanton, California for anexperienced Contract Lab Chemist (Technician).As a Contractor Technician in the AMS Analytical group, you will bepart of a team growing numerous brands across the portfolio, including Burts Bees, Kingsford,Hidden Valley, Pine-Sol, Brita and others. Through collaboration withScientists in the group and inter-functionally between groups, you will look tohelp create over $150MM of value per year. Daily responsibilities includeproduct and material analysis, method development and data analysis for avariety of products, focusing on those specifically from the Cleaning andProfessional Products Divisions. You will work closely with Scientists toprovide reports, identify issues and recommend next steps based onexperimentation. You will also have theopportunity to take on non-project specific initiatives within the departmentto increase the knowledge base and functionality of the group as a whole. We require someone with direct hands-on experience andexpertise 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 methoddevelopment, maintenance, supplies, repairs, purchases, and analyses, forvarious project teams. Various wet chemistry techniques including standardsample preparation methodologies such as accurate weighing, pipetting,centrifugation, dilution, extraction, drying and characterization methodologiessuch 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 orfluorescence instrumentation. Chromatography instruments (LC, GC, IC), relateddetectors, software programs, and techniques for compound identification andquantitation. 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 goodsindustries is highly desired: Household and institutional cleaning products,personal care, foods, charcoal, litter, water filtration, nutraceuticals, andprobiotics. Demonstrated knowledge of statistical analysis. Abilityto summarize and report analytical results, perform trend analysis, andimplement corrective action as needed. Strong willingness and aptitude to learn and master newtools and skills. Experience in working collaboratively withmulti-functional teams in a fast-paced environment, and in providingguidance/training for others on routine assignments. Ability to multi-task and manage work efforts on multipleprojects according to assigned priorities. Excellent adherence to lab and chemical safetyrequirements, company documentation policies, and a strong demonstrated workethic. Key Responsibilities (in descending order of importance): Accurately follow assay and safety procedures, and SOPs. Perform reliable sample preparation and analyticaltesting in the lab using various analytical chemistry techniques. Optimize sample preparation and analytical methodologiesas needed. Operate related equipment and software under peakperformance and safety conditions. Maintain equipment and software, upgrading and makingpurchase recommendations for new capabilities as necessary. Process and report analytical data using instrumentsoftware, Microsoft Excel, Word, and PowerPoint. Knowledge of Outlook,Microsoft Teams, and SharePoint preferred. Accurately and promptly instrument log data and labactivities in log or lab notebooks. Present data to project team members and management: Theability 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 wetchemistry lab such as in maintaining an organized, clean and safe labenvironment/workspace, ordering supplies, maintaining or repairinginstrumentation, performing calibrations, keeping instrument, and chemicalinventory records. MINIMUM REQUIREMENTS: Years and Type of Experience: 3-5+ years experience working in an analytical chemistrylab in a consumer goods, chemicals, crop protection, pharmaceutical company, orcontract research organization. Education Level/Degree: B.Sc. in Chemistry, Biochemistry, or related scientificfield.

Job DescriptionDescription: RxSight® is an ophthalmic medical technology corporation headquartered in Aliso Viejo, California that has commercialized the world’s first and only adjustable intraocular lens (IOL) that is customized after cataract surgery. The company’s mission is to revolutionize the premium cataract surgery experience by allowing surgeons to partner with their patients to achieve optimized results for every unique eye. OVERVIEW: The Manufacturing Injector Cleanroom Lead reporting to the Injector Cleanroom Supervisor will focus on fully understanding the company's technology and the processes necessary to manufacture it. With an emphasis on understanding process requirements, timing, cadence, training, available talent and application in real-time manufacturing. After training on manufacturing procedures, the Injector Cleanroom Lead can coordinate the execution of all processes to maintain production flow to meet company production quotas, timelines, and quality standards. The Injector Cleanroom Lead performs planning, coordination, and organization of daily manufacturing activities. Responsibilities include LAL packaging, accessories as well as special adhoc projects relating to manufacturing. A critical component of this position is maximizing the LAL sterile loads both from a maximum quantity and timing standpoint. Direct communication and support with supervisor. Requirements: ESSENTIAL DUTIES AND RESPONSIBILITIES: The Injector Cleanroom Lead will interact with the other functions including but not limited to Engineering, Quality, Chemist and R&D. It is expected that this individual will have the depth and breadth of experience to contribute to the oversight of the overall manufacturing of the LAL lenses. • The Manufacturing Injector Cleanroom Lead will interact with the other functions including but not limited to Engineering, Quality, Warehouse and Planning. It is expected that the lead will have the depth and breadth of experience to contribute to the overall processing of injectors and cartridges. The lead must complete the work with the highest Quality standards possible within the allowed time given to maintain the highest efficiencies., • Coordinates and communicates the execution of the following activities, to meet production goal timelines:, • Component Cleaning & Inspection, • Micro-Abrasion, • Abrasive Sieving, • Component Assembly, • Component Sealing, • Packaging Assembly, • The Lead may also be certified to train in the above activities., • Is responsible for collaborating and publishing a high-level weekly task plan for manufacturing activities., • Coordinates training of personnel to meet production goal timelines., • Coordinates production assistance in validation protocols, execution., • With guidance from engineering, perform tests, gather test data and records results in accordance with manufacturing requirements., • Support process improvement initiatives to enhance production efficiency, as well as ensure business continuity and regulatory compliance., • Past Medical Device Packaging Experience., • Three to five years related experience and/or training; experience in medical device packaging., • Training to be completed per the training plan for this position as maintained in the document control system. RxSight does not accept unsolicited resumes or candidate submissions from staffing agencies or search firms for any employment opportunities. All agency engagements must be authorized in writing for a specific position by RxSight’s Talent Acquisition department. Any resumes or candidate information submitted without such specific engagement will be considered unsolicited and the property of RxSight. No fees will be paid in the event a candidate is hired under these circumstances.

Job Description Job Title: Chemist Actalent is seeking an experienced Chemist to join our innovative team. In this role, you will play a critical part in supporting analytical testing and quality assurance for raw materials, in-process samples, and finished products. You’ll leverage advanced technologies and ensure strict compliance with cGMP standards to deliver exceptional results. Key Responsibilities • Perform and assist with analytical testing of raw materials, in-process samples, and finished products., • Operate and maintain advanced instrumentation including HPLC, GC, ICP, FTIR, TOC, MS, and dissolution apparatus., • Ensure compliance with cGMP regulations and adhere to all standard operating procedures., • Conduct peer reviews of technical data generated by other team members., • Develop, validate, and troubleshoot analytical methods to optimize accuracy and efficiency., • Execute method transfers between facilities and departments., • Author and update standard operating procedures and analytical methods., • Maintain and troubleshoot laboratory equipment and analytical instruments., • Perform and assist with equipment calibrations and qualifications., • Support laboratory management in preparing for internal, client, and regulatory audits.Essential Skills & Qualifications, • Proficiency in HPLC, GC, ICP, FTIR, TOC, MS, and dissolution apparatus., • Strong knowledge of cGMP regulations and quality standards., • Ability to critically review and validate technical data., • Hands-on experience in developing, validating, and troubleshooting analytical methods., • Skilled in authoring SOPs and analytical documentation. Additional Skills & Qualifications • Bachelor's Degree in Chemistry or related field., • 2-4 years experience in a chemistry laboratory or equivalent combination of education and experience. The role requires working in a laboratory setting with advanced analytical instruments. The Chemist will work in compliance with safety standards and company protocols, ensuring a clean and organized work environment. Job Type & Location This is a Contract position based out of IRVINE, CA. Pay and Benefits The pay range for this position is $32.00 - $36.00/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 IRVINE,CA. Application Deadline This position is anticipated to close on Dec 5, 2025. 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 due to a disability, please email for other accommodation options.

Job Description Seeking a motivated and detail-oriented Flavor Trainee to join our team. This is an excellent opportunity for an individual to utilize a degree in food science or a related field and/or significant hands-on experience in a flavor or food lab setting. This position will assist in the development and preparation of flavors under the supervision of the Senior Flavor Chemist. This entry-level role is ideal for candidates with a strong interest in flavor development. GENERAL DESCRIPTION OF DUTIES: The Flavor Trainee will be in charge of formula compounding, sensory, analytical and follow up documentation of flavors. General lab duties in flavor development lab, compounding, raw material procurement, management and restocking as needed. This individual must maintain a positive work atmosphere by behaving and communicating in ways that foster good relationships with those inside and outside the company, while achieving and enhancing performance standards. ESSENTIAL JOB FUNCTIONS: • Ability to compound simple to complex formulas with speed and accuracy while maintaining lab safety and proper PPE. Basic flavor modifications with substitution of raw materials, diluents or attribute change., • Ability to compound simple liquid blends, emulsions and spray dried flavors., • Understand and utility of the following equipment: density meter, pH meter, overhead stirrers, high shear mixer, homogenizer and spray dryer., • Creation of technical documentation as needed. This description reflects the principal functions of the job for the purpose of job evaluation. It should not be construed as a detailed description of all work requirements of the job, nor should it be construed as giving exclusive responsibility for functions described. REQUIREMENTS: • BS degree in food science, chemistry, or related disciplines., • Minimum 1-3 years’ experience in a flavor lab, or other product development experience., • Detail oriented, and good organizational skills., • Collaborate and cooperate in a team environment. PHYSICAL DEMANDS: • Must be able to work in a production and lab environment., • Ability to lift up to 25 pounds occasionally or as needed., • Mobility: Walking, standing, sitting, stooping, climbing, or bending., • Lifting and Carrying: The weight of objects that must be lifted, carried, pushed, or pulled. 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 Formulation R&D Chemist Job Description We are seeking a Formulation R&D Chemist with strong technical expertise with leadership responsibilities, overseeing R&D projects from concept to commercialization. Responsibilities • Develop and optimize formulations., • Supervise and mentor R&D staff., • Manage scale-up processes and troubleshoot manufacturing challenges., • Ensure compliance with FDA, EPA, and cGMP regulations., • Bachelor’s or Master’s degree in Chemistry or related field., • 8+ years of formulation experience or 5+ years with a Master's degree., • Strong regulatory knowledge and analytical skills., • Excellent project management and communication abilities., • Leadership skills preferred., • Experience in relevant industries such as personal care This is a Contract to Hire position based out of Corona, CA. Pay and Benefits The pay range for this position is $57.00 - $63.00/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 Corona,CA. Application Deadline This position is anticipated to close on Dec 5, 2025. 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 due to a disability, please email for other accommodation options.

Job Description Immediate opening for BS/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 DescriptionCompany Description CDL Sign-on Bonus: $3,000 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. Why join Clean Earth? In addition to competitive pay, we also offer: • Health benefits available Day 1, • 401k available Day 1, • 10+ paid holidays/year, • Free HAZWOPER training and certification, • Overtime opportunities, • Ability to be cross-trained into different roles Job Description PRINCIPAL DUTIES AND RESPONSIBILITIES: • Handles hazardous materials including inventorying, identifying, segregating, and packaging waste material in accordance with Lab Pack policies, procedures and practices and all applicable regulations., • Perform onsite services which may include waste collection, consolidation (i.e., bulking, repackaging), sampling, safety/compliance inspections, and other related activities required by the customer/contract., • Assists other business groups, i.e., Depack, Retail and HHW, for both internally and onsite as needed. • Preparing shipment of packaged waste by inspecting, labeling, marking, and loading into the transport vehicle, • Properly completes documentation including shipping papers, Land Disposal Restrictions (LDR’s), evaluations/certifications and other required documentation in accordance with appropriate regulations and procedures., • May require obtaining and maintaining a Commercial Driver’s License (CDL) with Hazmat Endorsement to legally operate Clean Earth vehicles necessary for transporting personnel and waste to and from customers’ job locations., • Follows, understands, and promotes by example, all Health & Safety /Job Safety Analysis (JSA’s) procedures including development of on-site Health &Safety plans/JSA’s as outlined in the procedures and policies. Basic Requirements: • An associate’s degree in general science (BS preferred) is required for the Lab Pack Chemist., • Driver’s License with clear record, • Moderate to extensive travel with 20% overnight travel, • Physical ability to lift and move material of various weights frequently exceeding 55 lbs. 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, tuition assistance, and a 401k with company matching. 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 Description Certified Group is committed to delivering expert solutions and quality testing our customers can feel confident in – on time, every time – so the world can trust in what it consumes. As a leading North American provider of laboratory testing, regulatory consulting, and certification & audit services, Certified Group includes Food Safety Net Services (FSNS), FSNS Certification & Audit, Certified Laboratories, EAS Consulting Group, and Labstat International Inc. Certified Group provides analytical testing and regulatory guidance services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, personal care, tobacco, nicotine, cannabis, and hemp industries. We are currently looking for a 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 1 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.

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 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- Tustin CA is searching for a SVOA GCMS Chemist I to prepare and analyze environmental samples following EPA protocols in adherence with Eurofins Quality Assurance programs and SOP’s. Chemist / Analyst duties will include, but are not limited to, the following: • Extract and prepare samples for analysis by Gas Chromatography Mass Spectrometry., • Evaluate chromatography and mass spectra 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., • Communicate with preparation team and project management team regarding work status., • 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., • Perform other laboratory duties as assigned.Qualifications The ideal candidate would possess the following qualifications • 1+ years’ experience operating a GC or GCMS in a production laboratory setting, required., • 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 experience and qualifications. Position is Full-time and eligible for overtime pay Candidate must be able to work one of the following two shifts: • Sunday thru Thursday, 1:00pm - 10:00pm 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, paid time off, 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! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: 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 2024, Eurofins generated total revenues of EUR 6.95 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 R & D Chemist analyzes, develops and improves existing and new products using existing and new raw materials and requires little to no supervision doing this work. Matches products supplied by customers and internal personnel from competitors. Calculates costing on all products developed. Directs the evaluation and testing of prototypes. May have some supervisory responsibility directing the work of Assistant and Associate R & D Chemists and technicians. Maintains contacts with Quality Control, Production, inter-company lab personnel, and Sales. Begins having some customer contact as well. This individual must maintain a positive work atmosphere by behaving and communicating in ways that foster good relationships with those inside and outside the company. Essential Job Functions: • Must demonstrate superior product development creativity.Develop and/or improve new and existing products including juice concentrates and flavors, based on defined customer or in-house requirements., • Must taste all products developed., • Begin to determine feasibility of certain projects based on company limitations., • Perform costing analysis on all work performed., • Create master formulas and compounding instructions as needed., • Prepare product specification sheets for submission to customers., • Begin to contact customers to determine their requirements with regard to product development., • Develop products that meet or exceed customer applications., • Begin to provide technical assistance to customers and brokers., • Perform shelf-life studies and stability testing of products to ensure they meet our claims., • Organize and establish guidelines, procedures and policies for handling all outgoing samples., • Assist QC and Production in first-time production of all new products., • Assume responsibility for all sample request inquiries in the absence of the R & D Manager., • Regular, punctual attendance., • B. S. in Food Science or related science discipline., • Minimum 4 years of experience as an R&D Chemist., • Must demonstrate excellent taste and aroma sense acuity., • Proficient in verbal and written English., • Some supervisory experience and/or training., • Must have visual acuity to evaluate sample appearance and use lab instruments., • Must be able to lift and carry up to 15 pounds occasionally. Company DescriptionGreat culture, offers stability and potential growth!Great culture, offers stability and potential growth!

Job Description A leading company in the cosmetics and chemical industry is seeking an experienced R&D Research Scientist to join its team. This role involves product formulation, ingredient research, and regulatory compliance to support the development and enhancement of cosmetics and chemical products. If you have a strong background in product development and formulation, this is a great opportunity to advance your career. Requirements Key Responsibilities: • Develop and improve formulations for cosmetics and chemical-based products., • Conduct research on raw materials, active ingredients, and product stability., • Ensure compliance with cosmetic regulations and safety assessments., • Collaborate with internal teams to enhance product performance and innovation., • Optimize product textures, stability, and functionality through ingredient research and testing. Qualifications: • Degree in Chemistry, Chemical Engineering, or a related field., • Experience in cosmetics or chemical product development., • Strong understanding of formulation design and ingredient interactions., • Knowledge of cosmetic industry regulations and safety assessments., • Ability to conduct raw material analysis and apply innovative research to product development. Benefits Benefits: • Comprehensive Health Insurance, • Paid Time Off (PTO), • 401(k) Retirement Plan, • Performance-Based Employee Awards, • Reimbursement for Business-Related Expenses, • Complimentary Breakfast & Lunch Provided If you are passionate about cosmetic and chemical innovation and eager to contribute to a cutting-edge R&D team, apply today.

Job DescriptionCompany Description CDL Sign-on Bonus $3,000 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. Why join Clean Earth? In addition to competitive pay, we also offer: • Health benefits available Day 1, • 401k available Day 1, • 10+ paid holidays/year, • Free HAZWOPER training and certification, • Overtime opportunities, • Ability to be cross-trained into different roles 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. 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 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, tuition assistance, and a 401k with company matching. 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 Description Exciting Opportunity to Join Our Legacy of Environmental Leadership! About Us: At Arcwood Environmental, we are more than just a company; we are pioneers in industrial waste management, committed to creating a cleaner, safer world. Since our inception during the environmental movement of the 1970s, we've been at the forefront of solving complex environmental challenges. Headquartered in Indianapolis, Indiana with a dedicated team of 2,000+ employees spread across the United States, we provide innovative and compliant solutions to thousands of clients in diverse industries. Why Arcwood? • Impactful Work: Be part of a team that makes a real difference. Our comprehensive services range from hazardous waste management and emergency response to onsite support and technical solutions, allow us to solve our customers' waste challenges. We are part of the solution. We don't generate any waste ourselves., • Growth Opportunities: At Arcwood, your contribution is valued beyond your job title. We believe in the power of continuous learning and growth, encouraging every employee to expand their skills and take on new challenges., • Safety First: Your health and safety are our top priorities. We foster a culture where every employee is empowered to act safely and ensure the well-being of their colleagues. Our mantra is Safe and Compliant, Always., • Collaborative Environment: Together we can achieve much more. Join a supportive and dynamic team where your ideas and efforts are recognized and rewarded. Our Commitment: We are dedicated to fostering an inclusive and innovative workplace where every employee can thrive. As part of our team, you will have the freedom to contribute your expertise wherever needed, ensuring the success of our mission to protect the environment. Our Vision: Our vision is to be the most trusted partner in the environmental services industry. We put our customers first and deliver agile, sustainable, and innovative solutions. We commit to nurturing top talent and creating lasting value for our customers, shareholders, communities, and the planet. Our Ownership: Arcwood Environmental is backed by the EQT Infrastructure VI fund, enhancing our capabilities, and expanding our reach. EQT is a dynamic global investment powerhouse managing EUR 232 billion in assets (EUR 128 billion fee-generating). With a focus on Private Capital and Real Assets, EQT owns and supports leading companies across Europe, Asia-Pacific, and the Americas, fostering sustainable growth, operational excellence, and market leadership. This exciting ownership positions us for continued impacts and growth in the future. Field Chemist As a Field Chemist you will be responsible for sorting and transporting hazardous and non-hazardous materials and waste, always ensuring compatibility and safety in all processes for each service provided to customers. Essential Functions & Requirements: • Prioritizes health and safety by adhering to policies, processes, and maintaining safe practices at all times, • Assists in the segregation of chemicals by hazard class and packs compatible materials in appropriate containers and prepares for transportation; completes necessary paperwork for each job, • Determines and loads supplies needed for job completion and travels to various industry, laboratory, and educational sites to perform lab pack services, • Assists in characterizing materials at field project sites, • Adheres to proper placarding and load segregation requirements when transporting hazardous materials, • Develops good customer relations by effectively communicating with site points of contact and others at customer location / site, • Appropriately directs Field Technicians / Drivers who are assisting with waste collection, • Maintains an introductory knowledge of high-hazard materials management / assessment and cylinder handling, • Maintains the ability to travel to support outside locations as needed, • In lieu of degree 2+ years of related experience (required), previous experience in lab packing or environmental waste (preferred), • Valid Driver's License and ability to obtain a Class B CDL with Hazmat endorsement within 6 months of hire date (required), • Ability to work in a constant state of alertness and in a safe manner, • Ability to develop a working knowledge of all Federal, State, and local laws and regulations pertaining to the Environmental Services industry, • Excellent interpersonal skills to effectively communicate with internal and external customers, • Due to the potential exposure to atmospheres/waste/materials this position requires individuals to be clean shaven at all times in order to don a respirator for protection. Benefits, Compensation, & Workforce Diversity: Arcwood offers competitive pay and bonus incentives. Benefits include choice of medical, dental, and vision plans, flexible spending or health savings accounts, employee and dependent life insurance, short and long-term disability, 401(k) savings plan with 7% company match, and tuition reimbursement. Equal Opportunity Employer - Veterans & Disabilities A post-offer drug screen and background check will be required.

Job Description Exciting Opportunity to Join Our Legacy of Environmental Leadership! About Us: At Arcwood Environmental, we are more than just a company; we are pioneers in industrial waste management, committed to creating a cleaner, safer world. Since our inception during the environmental movement of the 1970s, we've been at the forefront of solving complex environmental challenges. Headquartered in Indianapolis, Indiana with a dedicated team of 2,000+ employees spread across the United States, we provide innovative and compliant solutions to thousands of clients in diverse industries. Why Arcwood? • Impactful Work: Be part of a team that makes a real difference. Our comprehensive services range from hazardous waste management and emergency response to onsite support and technical solutions, allow us to solve our customers' waste challenges. We are part of the solution. We don't generate any waste ourselves., • Growth Opportunities: At Arcwood, your contribution is valued beyond your job title. We believe in the power of continuous learning and growth, encouraging every employee to expand their skills and take on new challenges., • Safety First: Your health and safety are our top priorities. We foster a culture where every employee is empowered to act safely and ensure the well-being of their colleagues. Our mantra is Safe and Compliant - Always. Our Vision: Our vision is to be the most trusted partner in the environmental services industry. We put our customers first and deliver agile, sustainable, and innovative solutions. We commit to nurturing top talent and creating lasting value for our customers, shareholders, communities, and the planet. Our Ownership: Arcwood Environmental is backed by the EQT Infrastructure VI fund, enhancing our capabilities, and expanding our reach. EQT is a dynamic global investment powerhouse managing EUR 232 billion in assets (EUR 128 billion fee-generating). With a focus on Private Capital and Real Assets, EQT owns and supports leading companies across Europe, Asia-Pacific, and the Americas, fostering sustainable growth, operational excellence, and market leadership. This exciting ownership positions us for continued impacts and growth in the future. Field Chemist II Essential Functions & Requirements: • Ensures Health & Safety is the number one goal by following policies, processes, and acting in a safe manner at all times., • Segregation of chemicals by hazard class; packing compatible materials in appropriate containers and preparing for transportation; completing necessary paperwork per job., • Determines and loads supplies needed for job completion and travels to various industry, laboratory, and school sites to perform lab pack services., • Characterizing materials at field project sites., • Follows proper placarding and load segregation requirements when transporting hazardous materials., • Maintain good client relations by keeping client aware of progress and addressing any questions., • Directs Field Technicians/Drivers assisting with waste collection., • Introductory Proposal Preparation., • Assist in Training of Field Chemist 1, • Proficient in high hazard materials management/assessment and cylinder handling., • Must be able to perform EAP tasks., • 1 year of prior lab packing or environmental waste experience required., • Valid Driver's License, • Class B CDL w/Hazmat endorsement or able to obtain within 6 months of hire (required), • Ability to work in a constant state of alertness and in a safe manner, • Ability to develop a working knowledge of all Federal, State, and local laws and regulations pertaining to the Environmental Services industry, • Excellent interpersonal skills to effectively communicate with internal and external customers All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran or status as a qualified individual with a disability. A post-offer drug screen will be required.

Job Description GENERAL DESCRIPTION OF DUTIES: This position works in conjunction with Flavor Chemists to perform the activities of the department, including timely completion of customer samples in accordance with GMP and safety guidelines. Assists Flavor Chemists in daily work assignments. Cooperates with all other departments, promoting information exchange and teamwork within the department. The Assistant is responsible for the accuracy of batch formulation and compliance with company policy, GMP and safety procedures. Reports to the Flavor Chemist Supervisor but also receives instruction from Flavor Chemists. The Assistant must contribute to the efficient and profitable operation of R&D and must maintain a positive work atmosphere by behaving and communicating in ways that foster good relationships with co-workers and managers, while achieving performance standards. ESSENTIAL JOB FUNCTIONS: • Accurately compounds new and/or existing products, including juice concentrates and flavors, based on defined requirements and following specific instructions and formulas., • Performs all Q.C. analysis and required tests on every product compounded., • Ensures timely completion of assigned tasks., • Assists in the preparation and packing of stock samples., • Maintains sufficient stock of lab raw materials and supplies to fulfill customer requests., • Works in a fast-paced environment, walking and standing constantly throughout the day., • Maintains organized and clean working area., • Adheres to all safety procedures and policies., • Has regular, punctual attendance. REQUIREMENTS: • Degree in Science, some lab experience or a combination of both., • Good communication skills with proficiency in written and verbal English., • Proficiency in math using a calculator, including conversions and some Algebra., • Familiar with a lab environment and the metric system., • Ability to lift up to 25 pounds occasionally., • Some post high school education is highly desirable. 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 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 a ICP-MS Heavy Metals Chemist to join our growing team! JOB SUMMARY The ICP-MS Chemist will be responsible for testing sample utilizing ICP-MS instrumentation. ESSENTIAL RESPONSIBILITIES • Performs analysis using one or more of the following techniques: ICP-MS or other instrument in a timely fashion maintaining a high level of quality., • Performs non-routine analysis, as required., • Performs preliminary sample preparation, when needed., • Proactively assists in development and validation of methods, as required., • Ability to work with heavy volume., • Successfully participates in proficiency testing., • Participates in relevant ISO QA/QC activities and documentation thereof., • Reports results for tests., • Prepare standards and maintain their inventory., • BS degree in the Sciences, preferable in chemistry, • Minimum two (2) year experience in Instrumentation, • Must have experience with the following techniques: GC, LCMS, GCMS, GC, HPLC, ICP/MS, ICP-OES, UV-VIS, FTIR, Titration, Gravimetric Analysis., • 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, • 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

Job Description Millennium Health LLC is an accredited specialty laboratory with more than a decade of experience in medication monitoring and drug testing services, helping clinicians monitor the use and misuse of prescription medications and illicit drugs. The testing is used by healthcare professionals to obtain objective information about patients’ recent use of prescription medications and/or illicit drugs and helps monitor the effectiveness of treatment plans. GENERAL SUMMARY The Supervisor, Analytical Laboratory is responsible for oversight and management of performance for the analytical laboratory processes using immunoassay and/or LC-MS/MS technology. WORK SCHEDULE: Tuesday through Saturday, 4 pm- 12:30 am PST The following are intended to be examples of the accountabilities for which the person in this position is responsible. This position description is not intended to be complete or all-inclusive and does not preclude management from assigning other or related functions for which the individual has demonstrated competency through performance. • Responsible for day-to-day supervision of testing personnel and reporting of laboratory test results for all test methods performed under CLIA regulation., • Provides direct and constant supervision to Laboratory Technicians and Laboratory Assistants as required by applicable state and federal regulations., • Required to provide oversight to testing areas and other laboratory personnel as required by applicable state and federal regulations., • Responsible for monitoring test analyses using immunoassay and/or LC-MS/MS technology, and specimen examinations to ensure that acceptable levels of analytic performance are maintained., • Responsible for scheduling staff to accomplish production goals., • Responsible for ensuring that Laboratory Occurrence Management (LOM) forms are completed for anomalies and corrective action is documented., • Participates in process improvement activities such as quality, safety, document management and control, and proficiency testing., • Interacts with vendors on special projects such as test method validations and new equipment., • Responsible for technical studies designed to improve or validate clinical laboratory testing methods., • Assists with advanced troubleshooting issues involving equipment, instruments, and assay performance., • Ensures and assists with training of laboratory personnel as appropriate., • Ensures performance of preventative maintenance and calibrations on laboratory equipment and instruments. May contact vendors to initiate maintenance, repair and troubleshooting of instruments and equipment., • Writes Laboratory documents such as Standard Operating Procedures and departmental forms as needed and ensures they are current., • Responsible for performance evaluations of direct reports., • Required to follow all safety procedures, policies, precautions, and Quality Assurance guidance., • Participates in internal laboratory audits., • Other duties as assigned., • Fulfill the responsibilities defined under CLIA General Supervisor role:, • Must be accessible to the laboratory as needed for on-site, telephone, or electronic consultation and is responsible for day-to-day supervision or oversight of the laboratory operation and personnel performing testing and reporting test results., • Resolution of technical problems in accordance with policies and procedures established by the laboratory director or technical supervisor., • Monitoring of test performance., • Ensuring that remedial actions are taken when test systems deviate from the laboratory's established performance specifications., • Providing orientation of testing personnel., • Ability to ensure HIPAA, Confidentiality and Compliance policy, procedures, and standards are always adhered to. The Supervisor, Analytical Laboratory remains aware of evolving needs and opportunities, showing flexibility to support the Company’s success. Pursues educational opportunities to maintain advanced and up-to-date knowledge in the field. Performs all other related duties as required and assigned and understands that the items in this description are not all-inclusive. Requirements ESSENTIAL PHYSICAL & MENTAL REQUIREMENT • Minimum Bachelor's degree in a chemical, physical, biological or clinical laboratory science, • Current California CLS license (Generalist or limited Toxicologist Scientist, or Clinical Chemist Scientist)., • Out-of-state Medical Technologists can be considered if they obtain their California CLS within 6 months of hire., • Bachelor’s degree with 6+ years of CLS/MT experience OR Master’s degree with 4+ years of clinical laboratory experience OR PhD with 2+ years of clinical laboratory experience., • 2+ years experience post-CLS/ MT license required., • Supervisory experience is highly preferred., • Knowledgeable in laboratory methods and techniques., • Knowledgeable of equipment and supplies used in a laboratory., • Proficient in MS Applications (Word/Excel/PowerPoint/Outlook)., • Strong interpersonal skills and ability to communicate with all levels of employees., • Effective attention to detail with high degree of accuracy., • Demonstrated ability to effectively lead staff and manage projects., • Must maintain continuing education units required by California Department of Health Services. This position will require the following physical requirements: sitting (50 %), walking (30 %), standing (20 %), and lifting up to 50 lbs. Physical requirements will vary depending on departmental needs. This position will require the following mental requirements: The employee is expected to read and understand standard operating procedures (SOPs). The employee should be able to convert SOP instructions into work-related task Benefits • Medical, Dental, Vision, Disability Insurance, • 401k with Company Match, • Paid Time off and Holidays, • Tuition Assistance, • Behavioral and Health Care Resources POTENTIAL HIRING RANGE: • Salary Range: $125,000 - $135,000, • Night-Shift Differential: $10,000, • Offers are based on the skills, knowledge, and abilities of the selected candidate. Millennium Health is an Equal Opportunity/Affirmative Action Employer and E-verify participant. All qualified applicants will receive consideration for employment without regard to race, color, creed, sex, national origin, disability, gender identity, sexual orientation or protected veteran status. California Employee Privacy Notice - Millennium Health LLC

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 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 The Company Tupos Therapeutics is led by a seasoned team of drug hunters and developers with a proven track record of advancing transformative therapies. Our collective experience includes the discovery and development of first-in-class medicines such as vemurafenib and pexidartinib, along with multiple clinical-stage programs across diverse indications. Our founding team helped pioneer a paradigm-shifting approach to small molecule drug discovery—anchoring structure-based drug design in the identification and validation of novel chemical scaffolds, an innovation widely recognized as a major contribution to the field. At Tupos, we extend this legacy by integrating cutting-edge computational chemistry, machine learning, and a growing arsenal of advanced chemistry toolkits. This multifaceted approach enables us to tackle some of the most persistent challenges in drug discovery and accelerate the path from program initiation to clinical entry. Headquartered near the geographic center of the San Francisco Bay Area—with an easy commute from the Peninsula, East Bay, and South Bay—Tupos is advancing a pipeline of novel therapies that target key immunological pathways—powered by a robust discovery platform and deep domain expertise. The Opportunity We are seeking an accomplished and highly motivated Computational Chemist to join our discovery team and lead the design of novel small molecules across multiple therapeutic programs. The ideal candidate will bring deep expertise in computational chemistry and structure-based drug design, a creative and mission-driven mindset, and a strong track record of advancing programs from early discovery through development candidate nomination. This is a high-impact role with the opportunity to shape discovery strategy, collaborate closely with cross-functional teams, and contribute significantly to the development of transformative therapies in a fast-paced environment. Responsibilities • Design novel small molecules with exceptional potency, selectivity, and drug-like properties by applying cutting-edge computational and machine learning techniques, modern structure-based drug design methods, and deep SAR insights to drive innovation and differentiation., • Collaborate closely with cross-functional teams, including medicinal and synthetic chemistry, biology, DMPK, and translation medicine, to shape and execute discovery strategy, troubleshoot complex problems, and accelerate the progression of programs through key discovery milestones., • Integrate and interpret diverse data streams, including biophysical/chemical, cellular, ADME, pharmacological, and structural biology data, to refine compound design hypotheses and enable rapid, data-driven decision-making in a fast-paced environment., • Advance chemical series through iterative design cycles, proactively identifying and addressing liabilities related to efficacy, selectivity, pharmacokinetics, and developability, while contributing to intellectual property strategy and creation., • Maintain fluency with emerging tools, technologies, and scientific literature in computational chemistry, machine learning, and drug discovery to bring forward novel approaches and continuously improve internal capabilities., • Clearly and effectively communicate scientific insights, strategic recommendations, and project progress through written reports, team discussions, and internal or external presentations. Qualifications • Ph.D. in Computational Chemistry, Structural Biology, Medicinal Chemistry, Theoretical Chemistry, or a related discipline, with 5+ years of industry experience in small molecule drug discovery., • Proven expertise in modern computer-aided drug discovery, including structure-based drug design, SAR analysis, and optimization of pharmacokinetic and physicochemical properties., • Demonstrated success in advancing small molecule programs from hit identification through lead optimization and development candidate nomination., • Experience collaborating in multidisciplinary teams and deep understanding of drug discovery principles, including ADME, pharmacology, and safety profiling, with the ability to synthesize complex datasets into clear, actionable design strategies., • Proficient in using industry-standard computational tools and capable of scripting to automate workflows and analyze large datasets., • Strong record of scientific communication, including authorship of publications, patent filings, and internal reports or presentations., • Strategic thinker with excellent problem-solving skills, scientific curiosity, and the ability to thrive in a fast-paced, collaborative environment., • Prior experience in immune-related indications or emerging therapeutic modalities such as targeted protein degradation or molecular glues is highly desirable., • Familiarity with AI/ML approaches that can meaningfully accelerate small molecule discovery, such as generative modeling, property prediction, structure-focused learning, and integration of multi-modal datasets, is a strong plus. Qualifications • Ph.D. in Immunology or a related field, with 8+ years of relevant experience in a biopharma or biotechnology setting; experience in early drug discovery is strongly preferred., • Deep expertise in immunology, with a strong understanding of immune signaling pathways, disease mechanisms, and immune modulation strategies., • Demonstrated success in designing and interpreting in vitro, in vivo, and ex vivo studies to support target validation, mechanism-of-action, and biomarker development., • Experience with a range of immunological assays (e.g., flow cytometry, cytokine profiling, cell co-culture systems) and disease-relevant models., • Proven track record of advancing immunology-focused programs through early discovery to development candidate nomination., • Strong leadership skills, with experience managing or guiding scientific teams and external collaborators., • Effective cross-functional collaborator with the ability to influence decision-making across disciplines including chemistry, translational science, and clinical development., • Excellent scientific communication skills, with experience presenting at internal governance meetings, external conferences, and contributing to peer-reviewed publications. Benefits and Pay The expected salary range for this position is $160,000 - $200,000. We encourage candidates of all levels to apply as there is sometimes flexibility on job level and responsibilities. Compensation and title will be based on a variety of factors, including experience, qualifications, and other job-related factors permitted by law. This position is also eligible for an annual bonus, equity, paid time off, and a benefits package. Benefits include company-subsidized medical, dental, and vision plans, and 401(K) matching. Employees may participate in benefit plans, subject to the terms and conditions of the applicable plans. Tupos Therapeutics is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. To all recruitment agencies: Tupos Therapeutics does not accept agency resumes. Please do not forward resumes to our jobs alias or to Tupos Therapeutics employees. Tupos is not responsible for any fees related to unsolicited resumes.

Job DescriptionYoh is seeking a Formulation Cosmetic Chemist to support a Cosmetic Manufacturer that specializes in personal care products located in Southern California, a hub for the beauty industry. Hand on experience with OTC SPF skin care cosmetics will be needed. This individual will be working on innovation, creating new textures, and concepts to keep our R&D with cutting edge formulation. We will also need their help in creating marketing sheet to present to our customers in innovation seminars. Please if you have hands on experience with OTC skin care cosmetics! Industry: Cosmetics Location: Los Angeles, CA Type: Direct Hire Shift: Monday-Friday: 8:00am-5:00pm KEY JOB RESPONSIBILITIES: • Develop new SPF skin care formulas and reverse engineered formula based on customer’s briefs and price target., • Reformulate and improve existing formulas., • Follow new trends closely with new products launches, ingredients and new concept such as “free from” claims., • Be familiar with the formulation restrictions using these claims., • Be familiar with cosmetic ingredient especially their function, delivery system, interaction depending of media/base., • Meet with suppliers and keep product files (clinical and regulatory)., • Work on Innovation, create new textures, concepts, actives to keep our R&D with cutting edge formulation., • Help creating marketing sheet to present to our customers in innovation seminars., • Request raw material pricing and input in our pricing matrix., • Evaluation/Selection/Advice regarding testing; Claims, Safety, Microbiology., • Assist Regulatory department requesting all the necessary ingredient information., • Be flexible with project priorities as they vary from time to time and manage a large workload under tight timeline., • Be able to make decisions to troubleshoot production or compounding. Improve and/or revise manufacturing/filling process if needed., • Work closely with our chemists to help on challenging projects or when needed., • Work closely with our Quality department to improve knowledge about new formulas, establishing standards., • Maintain the laboratory clean and organized, respecting GLP’s.QUALIFICATIONS:, • Bachelor of Science or higher degree in chemistry or related field., • SPF skin care formulation experience., • Creative thinking, technical writing, and organizational skills., • Industry experience on the bench formulating., • Knowledge of skin care cosmetic/personal care raw materials, functionality, and interactions., • Understanding of emulsion and surfactant technology as well as general formulation techniques., • Must be familiar with regulation for US market and other countries for globally approved formulas, especially for the natural and organic market (NSF, USDA/NOP, NPA).#IND-SPG Estimated Min Rate: $90000.00 Estimated Max Rate: $95000.00 What’s In It for You? We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include: • Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week), • Health Savings Account (HSA) (for employees working 20+ hours per week), • Life & Disability Insurance (for employees working 20+ hours per week), • MetLife Voluntary Benefits, • Employee Assistance Program (EAP), • 401K Retirement Savings Plan, • Direct Deposit & weekly epayroll, • Referral Bonus Programs Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Visit to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants 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. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice: Company DescriptionFounded in 1940, Yoh operates from 75 locations throughout North America and is headquartered in Philadelphia, PA. Yoh was the nation’s first technology staffing firm. As a business unit of Day & Zimmermann, Yoh has a flourishing global footprint, as our parent company operates from more than 150 worldwide locations. Company Website: in 1940, Yoh operates from 75 locations throughout North America and is headquartered in Philadelphia, PA. Yoh was the nation’s first technology staffing firm. As a business unit of Day & Zimmermann, Yoh has a flourishing global footprint, as our parent company operates from more than 150 worldwide locations.\r\nCompany Website:

Job DescriptionSalary: up to 85,000 non negotiable Position Title: Sr Chemist Reports to: Vice President of R&D Department: R&D (Research and Development) Local Candidates Only Key Responsibilities: Develop new formulas and reverse engineered formula based on customers briefs and price target. Be very careful about customers no-no lists. Reformulate and improve existing formulas. Follow new trends closely with new products launches, ingredients and new concept such as free from claims. Be familiar with the formulation restrictions using these claims. Be familiar with cosmetic ingredient especially their function, delivery system, interaction depending of media/base. Meet with suppliers and keep product files (clinical and regulatory). Work on Innovation, create new textures, concepts, actives to keep our R&D with cutting edge formulation. Help creating marketing sheet to present to our customers in innovation seminars. Request raw material pricing and input in our pricing matrix. Evaluation/Selection/Advice regarding testing; Claims, Safety, Microbiology. Assist Regulatory department requesting all the necessary ingredient information. Be flexible with project priorities as they vary from time to time and manage a large workload under tight timeline. Be able to make decisions to troubleshoot production or compounding. Improve and/or revise manufacturing/filling process if needed. Work closely with our chemists to help on challenging projects or when needed. Work closely with our Quality department to improve knowledge about new formulas, establishing standards. Represent Cosmetix West during cosmetics events such as suppliers seminars, SCC events, CEW, ICMAD, or other conferences or shows. Networking is a big part of our business model. Be able to understand Cosmetix West business model and new directions taken to insure easy transition, and success. Maintain the laboratory clean and organized, respecting GLPs. Qualifications: BS or more in chemistry or related field.

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, • 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, • 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.