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Senior Quality Lead

Job in 4040, Basel, Kanton Basel-Landschaft, Switzerland
Listing for: Flexsis
Full Time position
Listed on 2026-08-22
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst, Quality Engineering, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 150000 - 190000 CHF Yearly CHF 150000.00 190000.00 YEAR
Job Description & How to Apply Below

Flexsis is a company of the Interiman Group, one of the leading providers of personnel services in Switzerland. Thanks to our solid expertise as well as the competencies within the Interiman Group, we offer tailored solutions in personnel consulting.

For our client Roche in Basel
, we are looking for a reliable and motivated (m/f/d)

Senior Quality Lead
  • Start Date:

    asap
  • Latest Possible

    Start Date:

    01.10.2026
  • Planned Duration of Employment: 1 year
  • Extension: possible
  • Workplace:
    Basel
  • Home Office:
    Yes: 2 days a week
Tasks & Responsibilities:
  • Establish relationships with business stakeholders and lead the development of molecule/product/process/affiliate-level approaches with appropriate measures (CtQ Factors)
  • Analyze quality data to identify trends and risks, providing insights to business partners
  • Delivery of Activities to Assess Quality Status
  • Lead and perform complex audits and quality assessments.
  • Synthesize individual audit issues into systematic conclusions and present findings and associated risks to senior stakeholders, ensuring quality data fulfills regulatory requirements and supports organizational goals
  • Demonstration of Implementation to Health Authorities
  • Play a lead role in inspection preparation and management.
  • Provide training to staff and ensure relevant materials are prepared for regulatory review
  • Execution of PDQ Goals
  • Lead assigned goals and initiatives and drive the development or revision of PDQ processes
Must Haves:
  • Bachelor’s degree or equivalent in a scientific or quality-related field. Advanced degree preferred
  • Significant experience in the pharmaceutical / biotech / medical device industry, including knowledge of the end to end development and operationalisation of products, and the associated GxP regulations and considerations (e.g., GCP,GVP, IVD/MD Regulations)
  • Min. 5 years experience in leading GxP audits and managing complex quality projects
  • In-depth knowledge of drug development processes and global regulatory landscapes
  • Good understanding of Information Systems, e.g., audit management and analysis reporting tools
  • Understanding of business operations and strategies
  • Fluency in written and spoken English; bi or multi-lingual skills are desirable
  • Clinical Operations experience or quality function in system validations
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Position Requirements
10+ Years work experience
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