QC Laboratory Analyst - Wet Chemistry & GMP Focus

Actalent; St. Louis (MO); In loco; USD 36.000 - 39.000; Tempo pieno

Vantaggi offerti da questo lavoro

Medical benefits

401(k)

Life Insurance

PTO

Descrizione del lavoro

Actalent's Saint Louis, MO QC Laboratory Analysts perform analytical testing on raw materials, in-process, and finished product samples in a fast-paced QC lab. The role emphasizes wet chemistry, compendial methods, and data review, with training on HPLC, GC, IR, and UV under supervision.

Second shift, on-site in Saint Louis, MO, with potential overtime and shift flexibility. The position is contract-to-hire, offering growth within a GMP/FDA-regulated environment.

Competenze

• Bachelor's degree in Chemistry, Biology, or related field required.
• 3 years of QC experience in an FDA-regulated environment preferred.
• Proficiency with wet chemistry or instrumental methods.
• Experience documenting work in GMP/FDA-compliant systems.

Mansioni

• Perform analytical testing on materials and finished products in QC lab.
• Complete sample preparation with proper labeling and handling.
• Conduct wet chemistry and compendial methods per procedures.
• Document testing activities and results adhering to GMP/FDA requirements.
• Review data for accuracy and compliance with specs.
• Maintain clean, organized lab areas and assist in OOS investigations.
• Learn and perform instrumental analyses (HPLC, GC, IR, UV) under supervision.
• Support production timelines and communicate testing status to team.

Conoscenze

Hands-on Chemistry

Data Recording

Attention to Detail

Analytical Chemistry

FDA GMP Knowledge

Team Collaboration

Flexibility

Formazione

Bachelors degree in Chemistry, Biology, or related

Strumenti

HPLC

GC

IR

UV

Descrizione del lavoro

Actalent's Saint Louis, MO QC Laboratory Analysts perform analytical testing on raw materials, in-process, and finished product samples in a fast-paced QC lab. The role emphasizes wet chemistry, compendial methods, and data review, with training on HPLC, GC, IR, and UV under supervision.

Second shift, on-site in Saint Louis, MO, with potential overtime and shift flexibility. The position is contract-to-hire, offering growth within a GMP/FDA-regulated environment.