Deputy Qualified Person (QP)

apartmentgloor&lang AG placeSolothurn descriptionUnbefristet calendar_month 

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
  • Maintain strong shop floor presence, ensuring compliance and identifying improvement opportunities
  • 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
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