Quality & Compliance Consultant

What you will do

Working with the practice lead, your role as Quality & Compliance Consultant is to:

• Carry out audits and gap analyses (GMP, GAMP, 21 CFR Part 11)
• Strengthen and optimise the quality management system (QMS)
• Implement Data Integrity programmes (ALCOA+)
• Support change controls and deviation management
• Review and harmonise documentation and procedures
• Prepare teams for inspections (ANSM, EMA, FDA)

Your profile

• MSc-level degree in pharmacy, life sciences, quality or process engineering
• Experience in quality assurance in a GMP environment
• Professional French and English

You are recognised for the following qualities:

• Teaching skills and a listening ear
• Rigour and critical thinking
• At ease in writing and speaking
• Able to lead change

Your working environment

About C-Validation:

• An engineering firm founded and run by engineers who are still active in the field
• 4 areas of expertise: Commissioning, Qualification & Validation, Engineering Consultancy, Quality & Compliance
• Clients in Life Sciences, Supply Chain and Engineering
• Over 50 years of combined experience in the team
• A fast-growing company, hiring to keep developing

About the team:

The Quality & Compliance team strengthens our clients’ Quality systems: compliance reviews, internal audits, gap analysis, Data Integrity and CSV, inspection preparation. It works around four themes:

• audits and gap analyses
• the quality management system (QMS)
• data integrity (ALCOA+) and CSV
• inspection preparation and team training

You work closely with our clients’ Quality teams and with our technical practices.

Working arrangements:

• Location: Entzheim (France) · client sites
• Contract type: Permanent
• Expected start date: As soon as possible
• Work mode: Hybrid: Entzheim office and client sites
• All our positions are open to people with disabilities.

Don’t wait: join a fast-growing company where every file carries the name of the person who ran it.