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Deputy qualified person (qp)

Solothurn
gloor&lang AG
EUR 83’232.9 pro Jahr
Inserat online seit: 8 April
Beschreibung

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 industryMinimum 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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