QC Analytical Associate — Fast-Paced Lab Impact

Bristol Myers Squibb

Leiden

Hybrid

EUR 45,000 - 65,000

Full time

6 days ago
Be an early applicant
Application generator

Stand out for this role — generate a tailored resume and cover letter in about a minute.

Get past ATS filters

Job summary

Bristol Myers Squibb seeks a QC Analyst to support in-process, final product, and stability testing, and data review across GMP documentation. You will assist with method transfer, deviations, and continuous improvement initiatives.

Qualifications include a Bachelor’s in science and 2+ years in analytical testing within regulated environments. The role emphasizes teamwork, accuracy in data, and adherence to regulatory standards.

Qualifications

  • Ability to understand, interpret and apply Global Regulatory and cGMP requirements.
  • Knowledge of LIMS, ELN and laboratory data analysis systems preferred.
  • Problem-solving ability, technically adept and logical.
  • Ability to communicate effectively with peers, department management and cross-functional peers.
  • Experience with writing technical documents preferred.
  • Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.

Responsibilities

  • Perform routine testing of in-process, final product, and stability samples.
  • Perform testing for method transfer/validation/verification.
  • Perform data verification, data review and review of GMP documentation for general methods.
  • May perform document revision, project, CAPA and deviation/investigation related tasks and/ or continuous improvement efforts.
  • Train analysts on general job duties.
  • Perform other tasks as assigned.

Skills

Regulatory knowledge
cGMP knowledge
LIMS experience
ELN familiarity
Data analysis
Documentation writing
Team collaboration
Time management

Education

Bachelors in science
MLO Level 4 or equivalent

Tools

LIMS
ELN
HPLC/UPLC
qPCR
ELISA

Job description

Bristol Myers Squibb seeks a QC Analyst to support in-process, final product, and stability testing, and data review across GMP documentation. You will assist with method transfer, deviations, and continuous improvement initiatives.

Qualifications include a Bachelor’s in science and 2+ years in analytical testing within regulated environments. The role emphasizes teamwork, accuracy in data, and adherence to regulatory standards.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

QC Analytical Specialist: Data-Driven Lab Impact
QC Analytical Specialist: Data-Driven Lab Impact

Bristol Myers Squibb • Leiden

On-site
EUR 60,000 - 85,000
QC Analyst: Analytical Methods & Data Review
QC Analyst: Analytical Methods & Data Review

Bristol Myers Squibb EU Policy • Leiden

On-site
EUR 45,000 - 60,000
Senior QC Analytical Specialist
Senior QC Analytical Specialist

Bristol-Myers Squibb • Netherlands

On-site
EUR 65,000 - 90,000
Associate, QC Analytical
Associate, QC Analytical

Bristol Myers Squibb • Leiden

Hybrid
EUR 45,000 - 65,000
Specialist, QC Analytical
Specialist, QC Analytical

Bristol Myers Squibb • Leiden

On-site
EUR 60,000 - 85,000
Associate, QC Analytical
Associate, QC Analytical

Bristol Myers Squibb EU Policy • Leiden

On-site
EUR 45,000 - 60,000
Specialist, QC Analytical
Specialist, QC Analytical

Bristol Myers Squibb EU Policy • Leiden

On-site
EUR 45,000 - 70,000
QC Analytical Specialist — Data Review & Method Validation
QC Analytical Specialist — Data Review & Method Validation

Bristol Myers Squibb EU Policy • Leiden

On-site
EUR 45,000 - 70,000
Cell Therapy QC Microbiology Associate
Cell Therapy QC Microbiology Associate

Bristol Myers Squibb EU Policy • Leiden

On-site
EUR 30,000 - 42,000
Comprehensive benefits
Flexible work options
Senior QC Microbiology Specialist — In-Process Testing
Senior QC Microbiology Specialist — In-Process Testing

Bristol Myers Squibb EU Policy • Leiden

On-site
EUR 55,000 - 75,000