Spezialist:in Compliance

For a leading pharmaceutical company, we are looking for a qualified

• Location:
  
  Basel
• Start: ASAP
• Duration: 12 months
• Home Office:
  Possible, up to 40%

• Managing compliance records, mainly deviations, change controls, and CAPAs
• Acting as a key stakeholder interface for compliance records, including collaboration with QA, scientists, and senior management
• Facilitating and documenting root cause analyses
• Actively participating in Quality Review Boards and other strategic and quality-relevant governance bodies as required
• Supporting inspections, including preparation and presentation of records to internal and external auditors as well as health authority inspectors
• Critically evaluating work results and ensuring a high level of quality and compliance
• Playing a key role in maintaining and ensuring an appropriate GMP standard within the department
• Preparing and maintaining scientific and regulatory documentation related to compliance activities

• University degree (Bachelor’s, Master’s, or higher) in a relevant natural science field such as Chemistry, Pharmacy, Biology, or similar
• Candidates with a Laboratory Technician background may be considered if they bring more than 10 years of high-level GMP experience
• 3–5 years of professional experience within a regulated pharmaceutical or biotech environment
• Proven hands‑on experience working under cGMP regulations
• Solid experience with quality management systems, ideally Veeva Vault or a comparable QMS such as Track Wise
• Practical experience in managing compliance records, especially deviations, change controls, and CAPAs
• Strong communication skills with business fluency in English, both written and spoken;
  German is a strong asset
• Strong quality mindset, structured working style, and the ability to operate effectively in a regulated and dynamic environment

Interested? Then apply today. We look forward to hearing from you!