Qualified Person (qp)

Sanofi UK

Riells i Viabrea, Spain
Good manufacturing practices (gmp)
Quality management systems (qms)
Release batches of medicines
Our team plays a critical role as a bridge between production and quality, working closely with manufacturing units to ensure compliance with Good Manufacturing Practices (GMP) and Sanofi Group regulations

Job Summary

  • Our team plays a critical role as a bridge between production and quality, working closely with manufacturing units to ensure compliance with Good Manufacturing Practices (GMP) and Sanofi Group regulations.
  • Act as a Qualified Person (QP): release batches of medicines to the market, review release documentation, verify deviation closure, and ensure compliance with GMP, distribution requirements, and applicable regulations.
  • Lead and develop the team, fostering a culture of growth and responsibility, ensuring team knowledge, compliance with training, and adherence to procedures.

Matching Summary

Our team plays a critical role as a bridge between production and quality, working closely with manufacturing units to ensure compliance with Good Manufacturing Practices (GMP) and Sanofi Group regulations.

Skills & Requirements

Must-have

  • Good Manufacturing Practices (GMP)
  • Quality Management Systems (QMS)
  • release batches of medicines
  • HSE protocols
  • patient safety

Nice-to-have

  • continuous improvement mindset
  • collaboration and responsibility
  • analytical thinking
  • adaptable and open to change

Key Requirements

  • Bachelor's degree in Pharmacy or life sciences
  • Advanced English
  • Experience in Quality Assurance in pharmaceutical industry
  • Experience in team leadership or supervisory roles

Work Rights

Not specified

Tailored Resume

Cover Letter