On behalf of our client a well-established and steadily growing pharmaceutical company with a strong reputation in sterile manufacturing and clinical supply we are seeking an experienced Deputy Qualified Person (QP) to strengthen the Quality Assurance team.
This is a permanent opportunity within a close-knit family-style organisation offering hands-on impact visibility and the chance to actively shape quality and compliance standards in a dynamic GMP environment.
Your Key Responsibilities
Act as Deputy to the QP including batch certification under delegated responsibility
Review and approve quality documentation in line with GMP requirements
Act as the main compliance interface for clients and external partners
Drive and support Change Control processes and continuous improvement initiatives
Lead and manage deviations and investigations
Provide QA support across production laboratories and warehouse operations
Prepare and review certificates and client-facing documentation
Your Profile
Degree in Pharmacy Chemistry Life Sciences or equivalent
Proven experience as a QP or Deputy QP within the pharmaceutical industry
Minimum 5 years of GMP (cGMP) experience
Strong and demonstrable experience in sterile / aseptic manufacturing (essential)
Experience in team leadership or cross-functional coordination
Background in a CDMO environment is highly advantageous
Fluent French (C1 or higher) is mandatory with excellent written communication skills
Strong command of English
Confident user of standard IT tools (e.g. MS Office)
Why This Opportunity
Join a growing pharmaceutical company with international exposure
Work in a people-oriented agile environment with short decision paths
Take on a high-impact QA role with real ownership and visibility
Be part of an organisation active in clinical development and innovative pharmaceutical manufacturing
Sterile Manufacturing French-Speaking GMP PharmaOn behalf of our client a well-established and steadily growing pharmaceutical company with a strong reputation in sterile manufacturing and clinical supply we are seeking an experienced Deputy Qualified Person (QP) to strengthen the Quality Assuran...
Sterile Manufacturing French-Speaking GMP Pharma
On behalf of our client a well-established and steadily growing pharmaceutical company with a strong reputation in sterile manufacturing and clinical supply we are seeking an experienced Deputy Qualified Person (QP) to strengthen the Quality Assurance team.
This is a permanent opportunity within a close-knit family-style organisation offering hands-on impact visibility and the chance to actively shape quality and compliance standards in a dynamic GMP environment.
Your Key Responsibilities
Act as Deputy to the QP including batch certification under delegated responsibility
Review and approve quality documentation in line with GMP requirements