Job Description

Project

:
For our client, a large pharmaceutical company based in Basel, we are looking for a GMP Compliance Manager (m/f/d)

Background

:
The Material Supply Chapter in Basel is seeking a committed and motivated individual to actively develop and consolidate the GxP compliance culture within the team and in Material Management.
As part of this dynamic team, GMP Compliance Managers act as the central interface between various production and support areas. They are the first point of contact for all compliance issues and play a key role in ensuring smooth and innovative material supply. Close collaboration with cross-functional colleagues provides the opportunity to significantly shape and improve GxP compliance processes.

The ideal candidate

has a degree in life sciences or engineering, or a completed apprenticeship with extensive practical experience in technical processes in the pharmaceutical industry, and at least three years of professional experience in a cGMP environment, particularly in managing the implementation of cGMP requirements. Professional experience in quality assurance or quality control is required, as is initial professional experience in handling and operating automated systems in chemical or biotechnological development and production.

Main tasks and areas of responsibility:

Maintaining and deepening the GxP compliance culture within the Materials Supply Chapter and Materials Management Raising awareness, coaching, and supporting SMEs on GxP compliance and process improvement Tracking and expanding compliance-relevant KPIs and annual targets at MM LT level for the compliance department Processing and supporting deviations and conducting root cause analyses as well as implementing the necessary corrective and preventive measures Processing and supporting changes as well as implementing the necessary measures Planning, processing, and implementing technical changes within Materials Management Planning, processing, and implementing project work in the GMP environment Preparation, participation, and representation of the department in internal and external audits and inspections Creation, revision, and review of GMP documents Creation and revision of risk analyses as well as contact person for the Materials Management department for QRM topics Creation and optimization of training courses as well as conducting training courses in the Materials Management area GMP-compliant design of new and support of existing workflows Deviation, CAPA, and change management (Deviation/UPE and PE Management) Representation of the department during internal and external inspections

Must Haves:

Degree in Life Science or Engineering and/or training with extensive practical experience in the field of technical processes in the pharmaceutical industry At least 3 years of professional experience in a cGMP environment, particularly in managing the implementation of cGMP requirements Professional experience in Quality Assurance or Quality Control Initial professional experience in the handling and operation of automated systems in chemical or biotechnological development and production In-depth knowledge of the process in your own area of ??responsibility Very good verbal and written communication skills in German and English required Ability to work in a team Building a trusting and effective relationship with the interfaces Responsibility for decision-making in the above-mentioned tasks and activities

Reference No.: 924422SDA

Role

: GMP Compliance Manager

Industry

: Pharma

Place of work

: Basel

Workload

: 100%

Start

: 01.11.2025 (Latest possible start date: 01.12.2025)

Duration

: 9+

Application deadline

: 23.09.2025

Job Type: 100%

Work Location: On the road