Senior QC Analytical Scientist - 3rd Shift Group Leader
About The Position
Eurofins Professional Scientific Services is hiring a Senior QC Analytical Scientist to support and lead GMP testing of pharmaceutical in-process, raw material, intermediate, API, and stability samples. The role also supports investigations of invalid results and method transfer activities, and leads a team of 3–5 individual contributors. The position combines hands-on analytical work with team leadership and requires strong attention to detail and organizational skills. The role is permanent and full-time, based within commuting distance of Albany, New York. It works the 10:00 p.m.–8:30 a.m. overnight shift, with schedules available Sunday through Wednesday or Wednesday through Saturday. Overtime may be needed. Compensation is $38.00–$55.00 per hour, based on education, leadership background, and related industry experience.
Requirements
- Bachelor's degree in Chemistry, Pharmaceutical Sciences, Life Sciences, or a related field with at least 5 years of GMP/GLP testing experience; or a master's degree in one of these fields or a related field with at least 3 years of industry GMP/GLP testing experience.
- At least 3 years of industry experience with Liquid Chromatography (LC), conductivity, and titration.
- Experience using at least two of the following techniques or instruments: NMR, GC, ICP-OES, IR, RI, UV-Vis, or TGA.
- Knowledge and in-depth understanding of GMPs, ICH, and 21 CFR guidelines.
- At least 1 year of prior leadership experience.
- High attention to detail and excellent organizational skills.
Nice To Haves
- At least 2 years of successful leadership experience.
Responsibilities
- Conduct and review testing in accordance with approved methods, specifications, protocols, and compendial requirements.
- Follow GMP protocols and applicable regulations, including 21 CFR Parts 210 and 211, and ICH guidelines.
- Test pharmaceutical in-process, raw material, intermediate, API, and stability samples.
- Participate in method transfer, qualification, and verification studies.
- Support investigations of out-of-specification (OOS), out-of-trend (OOT), and invalid results.
- Use analytical techniques including NMR, GC, LC, ICP-OES, IR, RI, UV-Vis, conductivity, specific rotation, titration, and TGA.
- Qualify and manage reference standards.
- Conduct and review elemental impurities and residual solvent testing.
- Lead, manage, and develop a team of chemists.
- Act as a proactive point of contact for client and internal teams.
- Participate in new-hire interviews and onboarding as needed.
- Communicate administrative information and promote the company vision.
- Ensure laboratory operations meet high quality and efficiency standards.
- Perform administrative tasks that support team-member growth and development.
- Balance technical work with team leadership responsibilities.
- Foster morale, collaboration, and teamwork within the group.
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 and merit-based increases.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Senior
