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
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Act as Deputy to the QP, including batch certification under delegated responsibility
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Review and approve quality documentation in line with GMP requirements
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Maintain strong shop floor presence, ensuring compliance and identifying improvement opportunities
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Act as the main compliance interface for clients and external partners
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Drive and support Change Control processes and continuous improvement initiatives
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Lead and manage deviations and investigations
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Provide QA support across production, laboratories, and warehouse operations
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Prepare and review certificates and client-facing documentation
Your Profile
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Degree in Pharmacy, Chemistry, Life Sciences, or equivalent
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Proven experience as a QP or Deputy QP within the pharmaceutical industry
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Minimum 5+ years of GMP (cGMP) experience
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Strong and demonstrable experience in sterile / aseptic manufacturing (essential)
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Experience in team leadership or cross-functional coordination
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Background in a CDMO environment is highly advantageous
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Fluent French (C1 or higher) is mandatory, with excellent written communication skills
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Strong command of English
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Confident user of standard IT tools (e.g., MS Office)
Why This Opportunity?
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Join a growing pharmaceutical company with international exposure
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Work in a people-oriented, agile environment with short decision paths
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Take on a high-impact QA role with real ownership and visibility
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Be part of an organisation active in clinical development and innovative pharmaceutical manufacturing