Pharmacopeia QC Analyst
Job Responsibilities:
- Perform QC testing while strictly adhering to policies and safety procedures, SOP/SWI, Pharmacopeia, Federal Regulations, cGMP, and required training curricula.
- Perform all scheduled activities defined by laboratory management to meet demands of Production, Method Development, Validation, Independent Demand, and Stability program.
- Maintain safety and compliance of the laboratory work area.
- Perform cleaning of laboratories, equipment, and ancillary areas as required.
- Prepare for and operate QC equipment including pre and post-run setup and maintenance.
- Complete required paperwork and documentation as required.
- Troubleshoot sample discrepancies.
- Perform peer proofing on assays.
- Develop a working knowledge of appropriate compendia and/or regulatory guidance.
- Attend/contribute to scheduled team meetings, department, and safety meetings.
Skills:
- Raw material testing (pharmacopeia/wet chemistry assays) Water testing (TOC and Conductivity analysis)
- pH testing for media
- Buffer assays (titrations and photometric methods)
- Analytical equipment setup, usage, and maintenance
- Sample preparation and disposal
- Coordination of contract laboratory testing
- Chemical handling required with appropriate PPE provided. Vaccinations and vision examinations may be required based on specific job function.
Education/Experience:
- Bachelor’s degree in Chemistry or equivalent
- 2-4 years of relevant experience in cGMP controlled/pharmaceutical industry.
- Exceptional attention to detail and strong writing skills are crucial.
- The candidate must be able to work in a dynamic team environment with flexible schedule, including potential for weekends/holidays.
- Prefer local, open to candidates willing to relocate at their own expense
- Onsite • Education: BA Chemistry
- Must-Have Experience with: entry level with experience in Chemistry and Pharma
- Work Experience: 4 years (academia &; industry)
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