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Eurofins PSS is hiring a Senior QC Analytical Chemist Group Leader to support GMP testing of in-process, raw materials, intermediates, APIs, and stability samples. You will lead a 3-5 person team, investigate invalid results, and drive method transfer and verification studies with strong attention to detail.
The role requires BS/MS in Chemistry with 3+ years GMP/GLP experience and proficiency in LC, NMR, GC, ICP-OES, IR, RI, UV-Vis, and TGA.
Albany, NY, USA
Full-time
The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients 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 the products they supply are safe, their ingredients are authentic and labelling is 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 Senior QC Analytical Chemist Group Leader to support and lead GMP testing of pharmaceutical in-process, raw materials, intermediates, APIs, and stability samples. In addition, the successful candidate will support investigations of invalid results, method transfer activities, and lead a team of 3-5 individual contributors. This individual will have high attention to detail and possess excellent organizational skills.
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
Lead, manage, and develop a team of chemists.
Serve as a proactive and effective point of contact for client and internal teams.
Participate in new hire interviews and onboarding processes as needed
Disseminate administrative communications and promote company vision
Ensure adherence to highest quality and efficiency standards in laboratory operations
Perform administrative tasks to support team member growth and development
Balance technical work with team leadership responsibilities
Foster morale, collaboration, and teamwork with the group
BS in Chemistry, Pharmaceutical Sciences, Life Sciences, or related degree with 5+ years of GMP/GLP testing experience; OR MS in Chemistry, Pharmaceutical Sciences, Life Sciences, or related degree with 3+ years of industry GMP/GLP testing experience
3+ years 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
1+ years of prior leadership experience
This position is a permanent, full-time role with overtime as needed. The position will work 6am-6pm on a rotating schedule - the following shifts are available:
Sunday, Monday, Tuesday & every other Wednesday
Thursday, Friday, Saturday & ever other Wednesday
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
Compensation: $36.50-$41.00 per hour based on education, past leadership, and related industry experience