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Quality Control Specialist, Microbiology
NovartisQC Specialist II Microbiology overseeing compliance with GMP standards in pharmaceutical manufacturing. Supporting investigations and quality assurance across production and testing.
About the role
Key responsibilities & impact- Oversee production and testing activities to ensure cGxP compliance
- Support investigations into deviations and other quality events
- Review and approve production and quality control documentation
- Perform batch record reviews as required
- Approve quality control data and batch release documentation
- Report technical complaints and adverse events in a timely manner
- Contribute to audits and inspections within quality control
- Evaluate deviations and support operational excellence initiatives
Requirements
What you’ll need- Experience in quality control or analytical science & technology within pharmaceutical or biotechnology manufacturing
- Strong knowledge of Good Manufacturing Practice (GMP) requirements
- Solid technical understanding of laboratory instruments, devices, and digital systems
- Ability to work independently while collaborating effectively across teams
- Fluency in German and English, both written and spoken
Benefits
Comp & perks- Incentive program
- Modern company pension scheme
- On-site childcare facilities
- Learning and development opportunities
- Global career opportunities
- Market-oriented additional pay based on experience and qualifications
- Insurance plans
- Retirement plans
- Wellbeing resources
- Global recognition programs
- Flexible and hybrid working arrangements
- Minimum 14 weeks paid parental leave
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
CGxP ComplianceBatch Record ReviewQuality Control DocumentationTechnical Complaint ReportingAdverse Event Reporting
Soft Skills
Independent WorkTeam Collaboration