Qualified Person (qp)

Sanofi

Riells I Viabrea, Spain
Quality assurance in pharmaceutical industry
Gmp compliance
Product release
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, training compliance, 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

  • Quality Assurance in pharmaceutical industry
  • GMP compliance
  • Product release
  • Deviation management
  • CAPA implementation
  • HSE protocols

Nice-to-have

  • Continuous improvement mindset
  • Collaboration and teamwork
  • Adaptable and open to change
  • Patient safety focus

Key Requirements

  • Bachelor's degree in Pharmacy or life sciences
  • Advanced English proficiency
  • Experience in Quality Assurance
  • Team leadership experience

Work Rights

Not specified

Tailored Resume

Cover Letter