Senior Quality Lead
Job in
4040, Basel, Kanton Basel-Landschaft, Switzerland
Listed on 2026-08-22
Listing for:
Flexsis
Full Time
position Listed on 2026-08-22
Job specializations:
-
Quality Assurance - QA/QC
Data Analyst, Quality Engineering, Regulatory Compliance Specialist
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)
- 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
- 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
- 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
Position Requirements
10+ Years
work experience
Note that applications are not being accepted from your jurisdiction for this job currently via this jobsite. Candidate preferences are the decision of the Employer or Recruiting Agent, and are controlled by them alone.
To Search, View & Apply for jobs on this site that accept applications from your location or country, tap here to make a Search:
To Search, View & Apply for jobs on this site that accept applications from your location or country, tap here to make a Search:
Search for further Jobs Here:
×