QC Analytical Chemist Group Lead - GMP Lab Leadership

Eurofins

City of Albany (NY)

On-site

USD 52,000 - 58,000

Full time

23 hours ago
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Benefits offered by this job

Medical, dental, vision
401(k) with company match
Life & disability insurance
Paid vacation & holidays
Bonus eligibility

Job summary

Eurofins USA PSS Insourcing Solutions is seeking a QC Analytical Chemist Group Leader to oversee GMP testing of pharmaceutical samples and lead a 3-5 member team. The role involves investigations of invalid results, method transfer, and coordinating with clients while ensuring high quality laboratory operations.

The position works 6pm-6am on a rotating schedule; requires a BS/MS with GMP/GLP experience and strong LC, NMR, GC, and ICP-OES skills.

Qualifications

  • BS with 3+ years GMP/GLP testing or MS with 1+ years GMP/GLP testing.
  • Minimum 1 year LC, Conductivity, and Titration experience.
  • Proficiency with at least two techniques/instruments listed (NMR, GC, ICP-OES, IR, RI, UV-Vis, TGA).
  • Knowledge of GMP, ICH, and 21 CFR guidelines.
  • Prior leadership/mentoring experience.
  • Authorized to work in the United States without sponsorship.

Responsibilities

  • Conduct testing and review per approved methods and specs.
  • Follow GMP regulations and ICH guidelines in all activities.
  • Test samples including in-process, raw materials, intermediates, APIs, and stability.
  • Participate in method transfer, qualification, and verification studies.
  • Support investigations for OOS, OOT, and invalid results.
  • Lead a team of chemists and coordinate client communications.

Skills

Team leadership
GMP/GLP testing
Analytical thinking
ICH/regulatory knowledge
Client communication

Education

BS in Chemistry or Life Sciences
MS in Chemistry or Life Sciences

Tools

LC (Liquid Chromatography)
NMR
GC
ICP-OES
IR
RI
UV-Vis
TGA

Job description

Eurofins USA PSS Insourcing Solutions is seeking a QC Analytical Chemist Group Leader to oversee GMP testing of pharmaceutical samples and lead a 3-5 member team. The role involves investigations of invalid results, method transfer, and coordinating with clients while ensuring high quality laboratory operations.

The position works 6pm-6am on a rotating schedule; requires a BS/MS with GMP/GLP experience and strong LC, NMR, GC, and ICP-OES skills.

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