Job Description

A Chemist with 5+ year's experience in dietary supplement manufacturing is needed in the Vista, CA area. The Chemist will oversee analytical method development, validation, and routine testing of raw materials, in-process, and finished products to ensure compliance with cGMP and cGLP standards. This role supports both production and R&D through precise and timely analytical testing using techniques such as HPLC, UPLC_MS/MS, ICP_MS, and GC_MSMS, while managing investigatory processes for OOS/OOT results and driving continuous laboratory improvements.

Chemist Responsibilities:

• Develop, validate, and verify analytical methods for raw materials, in-process, and finished products using HPLC, UPLC_MS/MS, ICP_MS, and GC_MSMS.
• Perform routine and non-routine testing per established SOPs, ensuring accuracy, precision, and timely data reporting.
• Manage and review OOS investigations, analyze test results, trend data, and recommend corrective actions (CAPA) to resolve testing issues.
• Oversee instrument operation, maintenance, calibration, and troubleshooting, ensuring robust documentation and compliance.
• Coordinate laboratory activities including sample preparation, reagent handling, and final QC sample release in the absence of supervisory staff.
• Revise and create SOPs for analytical methods and ensure compliance with regulatory guidelines.
• Train and mentor junior staff on instrument usage, maintenance, and analytical methodologies.
• Communicate testing status and collaborate with cross-functional teams to drive method improvements and support stability studies.

Chemist Requirements:

• BS or MS in Chemistry, Biochemistry, Chemical Engineering, or related science field.
• Minimum 5 years of hands-on analytical laboratory experience in the dietary supplement (or related) industry.
• Demonstrated expertise in HPLC/UPLC and proficiency with at least two other analytical techniques (e.g., GC, ICP, FTIR, UV/VIS). MS techniques (e.g., ICP/MS, HPLC/MS, GC/MS/MS, or UPLC/MS/MS) highly desirable.
• Strong understanding of method development, transfer, and validation under cGMP/cGLP guidelines.
• Excellent computer skills with experience in Microsoft Word and Excel; knowledge of Access and PowerPoint is a plus.
• Ability to independently manage multiple projects in a fast-paced, deadline-driven environment with meticulous attention to detail.
• Strong critical thinking, problem-solving, and effective communication skills to collaborate across teams.

Benefits:

• Above Market Compensation: Earn a competitive salary commensurate with experience.
• Health and Wellness: Access to comprehensive health, dental, and vision insurance plans to keep you and your family healthy.
• Retirement Savings: Participate in a robust 401(k) plan with employer matching contributions to help secure your financial future.
• Work-Life Balance: Enjoy generous paid time off, flexible scheduling options, and a supportive work environment.

**Out of state candidates or candidates requiring relocation will not be considered at this time.**

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