Process & Compliance Manager

Description du poste

Jobdescription

For one of our clients, a global pioneer in
pharmaceuticals, we are currently looking for a Process &
Compliance Manager.

General
Information:

• Start
  Date: 15.02.2026
• Latest Possible Start
  Date: 01.03.2026
• Planned Employment
  Duration: 2 years with the possibility of
  extension
• Workplace: Basel
• Workload: 100%
• Home
  Office: max 20%
• Team: 8
  People
• Department: Material Supply Chapter
  (MMNGHA)
• Working
  Hours: Standard

About the job:

The Material Supply Chapter
in Basel is looking for a dedicated and motivated individual to
actively develop and strengthen the GxP compliance culture within
the team and in material management. As part of the dynamic team,
GMP Compliance Managers act at the central interface between
various production and support areas. You will be the primary
contact person for all process and compliance matters and play a
key role in ensuring a smooth and innovative material supply. Close
collaboration with colleagues across functions offers the
opportunity to significantly shape and improve GxP compliance
processes.

The ideal
candidate:

Holds a degree in Life Science or
Engineering, or have completed vocational training with extensive
practical experience in technical processes within the
pharmaceutical industry and at least three years of professional
experience in a cGMP environment, particularly in managing the
implementation of cGMP requirements. Experience in Quality
Assurance or Quality Control is required, as is initial experience
in operating automated systems in chemical or biotechnological
development and production.

Tasks
& Responsibilities:

• Maintaining
  and strengthening 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 developing
  compliance-relevant KPIs and annual targets at the MM LT level for
  the Compliance area
• Handling and supporting
  deviations, conducting root cause analyses, and implementing the
  necessary corrective and preventive
  measures
• Handling and supporting changes, and
  implementing the necessary measures
• Optimizing
  processes within materials management
• First
  point of contact for interfaces regarding material supply, process,
  and compliance issues.
• Planning, processing,
  and implementation of technical changes within Materials
  Management
• Planning, processing, and
  implementation of project work in the GMP
  environment
• Preparation, participation, and
  representation of the department at internal and external audits
  and inspections
• Creation, revision, and review
  of GMP documents
• Creation and revision of risk
  analyses, as well as serving as the contact person for Materials
  Management regarding QRM issues
• Development and
  optimization of training courses, as well as conducting training
  sessions in the area of Materials
  Management
• GMP-compliant design of new and
  support of existing workflows
• Deviation, CAPA,
  and change management (deviation/UPE and PE
  management)
• Representation of the department at
  internal and external
  inspections

Must
Haves:

• Degree in Life Science or
  Engineering and/or training with extensive practical experience in
  technical processes in the pharmaceutical
  industry
• Minimum of 3 years of professional
  experience in a cGMP environment, particularly in managing the
  implementation of cGMP
  requirements
• Professional experience in
  logistics, quality assurance, or quality
  control
• Initial professional experience in
  handling and operating automated systems in the chemical industry
  and/or biotechnological development and
  production
• Sound knowledge of the process in
  your area of responsibility
• Excellent verbal
  and written communication skills in German and English
  required
• Teamwork
  skills
• Building a trusting and effective
  relationship with interfaces
• Responsibility for
  decision-making in the above-mentioned tasks and
  activities

Sounds interesting? Apply
Now! We look forward to receiving your
application.

Application Submission Deadline:
22.01.2026