Cell Therapy QC Analyst – In-Process & Final Product

Bristol-Myers Squibb Co; New Jersey; In loco; USD 48.000 - 58.000; Tempo pieno

Vantaggi offerti da questo lavoro

Comprehensive benefits

Flexible Time Off

NJ site team environment

Descrizione del lavoro

Bristol Myers Squibb Co in Summit West, NJ, seeks a QC Analyst to support testing of in-process, final product, and stability samples. You will review data, verify GMP documentation, assist with method transfer and deviations, and train junior analysts.

Shift: Wed–Sat, 1:30pm–11:30pm. Qualifications include a Bachelor's degree in science and 2+ years in analytical QC, with experience in cell/molecular biology techniques and cGMP.

Competenze

• Bachelor's degree in science or equivalent.
• 2+ years of analytical testing or QC experience in a regulated environment.
• Experience with cell/molecular biology techniques (e.g., flow cytometry, qPCR).
• Understanding of cGMP regulatory requirements.

Mansioni

• Perform routine testing of in-process, final product, and stability samples.
• Perform data verification and GMP documentation review.
• Assist with method transfer/validation/verification and deviations.
• Train analysts on general job duties and maintain compliance.

Conoscenze

cGMP knowledge

Analytical testing

Data review

Communication

Problem solving

Formazione

Bachelor's degree in science

2+ years QC experience

Strumenti

LIMS

ELN

Descrizione del lavoro

Bristol Myers Squibb Co in Summit West, NJ, seeks a QC Analyst to support testing of in-process, final product, and stability samples. You will review data, verify GMP documentation, assist with method transfer and deviations, and train junior analysts.

Shift: Wed–Sat, 1:30pm–11:30pm. Qualifications include a Bachelor's degree in science and 2+ years in analytical QC, with experience in cell/molecular biology techniques and cGMP.