Quality Control Analyst

Sanofi UK

Cuautitlan Izcalli, Mexico
Onsite
Physicochemical and/or microbiology analysis
Cgmp and hse requirements
Validated laboratory methods
The Quality Control department is responsible for performing tests, analyses, and evaluations on bulk product, semi-finished product, finished product, critical systems samples, raw materials, and primary and secondary packaging material

Job Summary

  • The Quality Control department is responsible for performing tests, analyses, and evaluations on bulk product, semi-finished product, finished product, critical systems samples, raw materials, and primary and secondary packaging material.
  • Key responsibilities include executing analytical tests in a timely manner, ensuring compliance with cGMP and HSE requirements, and maintaining laboratory facilities and instruments in a quality and safe state.
  • Sanofi offers equal opportunities to all, encouraging employees to grow and develop diversified career paths within the organization.

Matching Summary

The Quality Control department is responsible for performing tests, analyses, and evaluations on bulk product, semi-finished product, finished product, critical systems samples, raw materials, and primary and secondary packaging material.

Skills & Requirements

Must-have

  • physicochemical and/or microbiology analysis
  • cGMP and HSE requirements
  • validated laboratory methods
  • raw data recording and integrity
  • laboratory instrument maintenance

Nice-to-have

  • decision making and problem analysis
  • continuous improvement orientation
  • vaccines and biologics experience

Key Requirements

  • Pharmaceutical industry analytical experience
  • Experience in physicochemical and/or microbiology
  • Bachelor's degree in chemical-pharmaceutical areas
  • Basic-intermediate English language skills

Work Rights

Not specified

Tailored Resume

Cover Letter