Night-Shift QC Analytical Chemist: GMP & LC/GC Specialist

LabRulez; City of Albany (NY); On-site; USD 33,000 - 43,000; Full time

Benefits offered by this job

Medical, dental, and vision options

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Annual bonus potential

Job summary

Eurofins PSS is hiring a QC Analytical Chemist to support GMP testing of pharmaceutical in-process, raw materials, intermediates, APIs, and stability samples. The role includes investigations of invalid results and involvement in method transfer.

This role requires attention to detail, strong organization, and knowledge of GMP/ICH guidelines. Responsibilities include testing using NMR, GC, LC, ICP-OES, IR, UV-Vis, RI, and other techniques, with BS or MS in Chemistry and GMP/GLP experience and US

Qualifications

• BS in Chemistry, Pharmaceutical Sciences, Life Sciences, or related degree with GMP/GLP testing experience.
• At least a year of industry experience with LC, Conductivity, and Titration.

Responsibilities

• Conduct testing per approved methods, specifications, protocols, and compendial requirements.
• Follow GMP regulations including 21 CFR Parts 210 and 211 and ICH guidelines.
• Test pharmaceutical samples including in-process, raw materials, intermediates, API, stability.
• 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, TGA, and more.
• Reference standard qualification and management.
• Elemental impurities and residual solvent testing and review.

Skills

Attention to detail

Organizational skills

GMP/GLP knowledge

Education

BS in Chemistry or related with 1 year GMP/GLP testing

MS in Chemistry or related with 6 months GMP/GLP testing

Tools

NMR

GC

LC

ICP-OES

IR

RI

UV-Vis

TGA

Job description

Eurofins PSS is hiring a QC Analytical Chemist to support GMP testing of pharmaceutical in-process, raw materials, intermediates, APIs, and stability samples. The role includes investigations of invalid results and involvement in method transfer.

This role requires attention to detail, strong organization, and knowledge of GMP/ICH guidelines. Responsibilities include testing using NMR, GC, LC, ICP-OES, IR, UV-Vis, RI, and other techniques, with BS or MS in Chemistry and GMP/GLP experience and US