Job Description

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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