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Analytical Chemist

Job in Hercules, Contra Costa County, California, 94547, USA
Listing for: Actalent
Full Time position
Listed on 2026-07-14
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist
  • Research/Development
    Biotech Research, Pharmaceutical Science/ Research, Regulatory Compliance Specialist, Lab Tech / Assistant
Salary/Wage Range or Industry Benchmark: 41328 - 48216 USD Yearly USD 41328.00 48216.00 YEAR
Job Description & How to Apply Below

Analytical Chemist – Job Summary

This bench-focused Analytical Chemist role centers on hands‑on work in a regulated laboratory, performing analytical testing with HPLC and LC‑MS to support product, process, and quality‑related studies. You will prepare samples and reagents, operate and maintain analytical instruments, generate and interpret data, and ensure all activities comply with GMP, GLP, and established laboratory procedures. The position suits someone with 1–2 years of direct industry experience who enjoys working in a fast‑paced, collaborative wet lab environment and contributing to high‑quality scientific outcomes.

Responsibilities
  • Perform routine analytical testing using HPLC and LC‑MS methods to support product, process, and quality‑related studies.
  • Prepare samples, reagents, calibration standards, and mobile phases in accordance with SOPs and approved methods.
  • Operate, maintain, and perform basic troubleshooting of HPLC and LC‑MS systems to ensure reliable performance.
  • Execute analytical assays and experiments following validated methods and established protocols.
  • Analyze chromatographic and mass spectrometry data and accurately document results in approved formats.
  • Record experimental activities and results in laboratory notebooks, LIMS, or other controlled documentation systems.
  • Support instrument qualification, calibration, and preventative maintenance activities as assigned.
  • Maintain strict compliance with GMP, GLP, and laboratory safety requirements at all times.
  • Assist with method transfers, SOP revisions, and laboratory investigations as needed to support ongoing projects.
  • Collaborate with scientists and cross‑functional teams to support project timelines and deliverables.
  • Contribute to maintaining clean, organized, and audit‑ready laboratory work spaces.
  • Participate in continuous improvement of analytical methods, workflows, and documentation practices where appropriate.
Essential Skills
  • B.S. degree in Chemistry, Biochemistry, Analytical Chemistry, or a related scientific discipline.
  • Minimum 1–2 years of direct industry experience operating HPLC and LC‑MS instrumentation in a regulated laboratory environment.
  • Demonstrated experience with sample preparation, instrument setup, sequence creation, data review, and basic troubleshooting.
  • Hands‑on experience performing analytical testing using HPLC and LC‑MS methods.
  • Experience working in a GMP, GLP, pharmaceutical, biotech, food, environmental, or contract research (CRO) laboratory environment.
  • Familiarity with chromatography data systems and electronic or paper‑based laboratory documentation practices.
  • Strong attention to detail with the ability to follow SOPs and maintain accurate, complete, and compliant records.
  • Ability to manage multiple priorities and deliver high‑quality work in a fast‑paced laboratory setting.
  • Solid understanding of laboratory safety practices and regulatory expectations in a GMP/GLP environment.
  • Strong communication and collaboration skills to work effectively with scientists and cross‑functional teams.
Additional

Skills & Qualifications
  • Experience with method qualification, verification, or validation activities.
  • Exposure to additional analytical techniques such as GC, ICP‑MS, UV‑Vis, or dissolution testing.
  • Experience with ELISA platforms or other complementary analytical systems.
  • Previous experience supporting quality control, manufacturing support, or product development programs.
  • Experience participating in instrument qualification, calibration, and preventative maintenance programs.
  • Comfort working with LIMS or other controlled documentation systems in a regulated environment.
  • Demonstrated ability to contribute to SOP revisions, method transfers, or laboratory investigations.
  • Interest in continuous improvement of laboratory workflows, data integrity, and documentation standards.
Work Environment

This role is fully onsite in a bench‑based wet laboratory environment five days a week. You will work in a regulated GMP/GLP setting that emphasizes safety, quality, and compliance in all activities. The position involves extensive hands‑on work with analytical instruments such as HPLC, GC, LC‑MS, ICP‑MS, ELISA platforms, UV‑based…

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