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About the Role
Eurofins PSS is hiring a QC Analytical Chemist to perform GMP testing of pharmaceutical samples, including in-process, raw materials, intermediates, APIs, and stability samples. This role also involves supporting investigations of invalid results and method transfer activities, requiring high attention to detail and excellent organizational skills.
Responsibilities
- Conduct testing and review in accordance with approved methods, specifications, protocols, and compendial requirements.
- Follow protocols for GMP regulations, including 21 CFR Parts 210 and 211, and applicable ICH guidelines.
- Test pharmaceutical samples including in-process, raw materials, intermediates, API, stability, and more.
- Participate in method transfer, qualification, and verification studies.
- Support investigations for OOS, OOT, and invalid results.
- Utilize various analytical techniques including: NMR, GC, LC, ICP-OES, IR, RI, UV-Vis, Conductivity, Specific Rotation, Titration, TGA, and more.
- Perform reference standard qualification and management.
- Conduct elemental impurities and residual solvent testing and review.
Requirements
- BS in Chemistry, Pharmaceutical Sciences, Life Sciences, or related degree with 3+ years of GMP/GLP testing experience; OR MS in Chemistry, Pharmaceutical Sciences, Life Sciences, or related degree with 1+ years of industry GMP/GLP testing experience.
- At least one year of industry experience with Liquid Chromatography (LC), Conductivity, and Titration.
- Proven experience utilizing at least two of the following techniques and/or instruments: Nuclear Magnetic Resonance (NMR), Gas Chromatography (GC), Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES), Infrared Spectroscopy (IR), Refractive Index (RI), Ultraviolet-Visible (UV-Vis), Thermogravimetric Analysis (TGA).
- Knowledge and in-depth understanding of GMPs, ICH, and 21 CRF guidelines.
Skills
- NMR
- GC
- LC
- ICP-OES
- IR
- RI
- UV-Vis
- Conductivity
- Specific Rotation
- Titration
- TGA
- GMP
- GLP
- ICH
- 21 CFR
Location
- Albany, NY
Work Type
- Permanent
- Full-time
- Overtime as needed
Experience Level
- 3+ years of GMP/GLP testing experience (BS)
- 1+ years of industry GMP/GLP testing experience (MS)
- 1+ year of industry experience with LC, Conductivity, and Titration
- Experience with at least two specified analytical techniques/instruments
Education Level
- BS in Chemistry, Pharmaceutical Sciences, Life Sciences, or related degree
- MS in Chemistry, Pharmaceutical Sciences, Life Sciences, or related degree
Salary/Compensations
- $35.50-$45.00 per hour
Benefits
- Comprehensive medical coverage, dental, and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
- Eligibility for yearly goal-based bonus & merit-based increases
About the Company
- Eurofins PSS focuses on professional growth and provides employees the ability to break into the biopharmaceutical industry and grow from the bottom up with supportive teams and tools.
- Eurofins Scientific is an international life sciences company providing analytical testing services to make life and our environment safer, healthier and more sustainable.
- Eurofins is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services.
- Eurofins is a global independent market leader in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
Equal Opportunity
- Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.