QC Analytical Chemist - 6am-6pm

About the role

The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we focus on your professional growth, providing the ability to break into the biopharmaceutical industry and grow from the bottom up. We have supportive teams and tools to invest in you while affording work‑life balance and a competitive benefits package. Eurofins Scientific is an international life sciences company providing analytical testing services across multiple industries to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure products are safe, ingredients authentic and labeling accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. Eurofins PSS is currently hiring for a QC Analytical Chemist to support GMP testing of pharmaceutical in‑process, raw materials, intermediates, APIs, and stability samples. In addition, the successful candidate will support investigations of invalid results and method transfer activities. This individual will have high attention to detail and possess 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
• Testing of 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
• Reference standard qualification and management
• 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 a 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 CFR guidelines
• Authorization to work in the United States indefinitely without restriction or sponsorship
• Preferred: At least a year of GMP experience

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

Pay

Compensation: $35.00‑$41.00 per hour based on