Computer System Validation Engineer
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Job Location:
Lucerne - Switzerland
Salary:
Not Disclosed
Posted on:
3 hours ago
Vacancies:
1 Vacancy
Job Summary
CK QLSare currently seeking a Computer System Validation (CSV) Engineer to join a Metrology & Validation team within Analytical Research & Development at a GMP-regulated pharmaceutical site in Switzerland.
This site-based role offers the opportunity to work closely with analytical laboratories quality IT and global validation partners ensuring analytical instruments and computerized systems remain in a state of permanent inspection readiness.
Key Responsibilities
This site-based role offers the opportunity to work closely with analytical laboratories quality IT and global validation partners ensuring analytical instruments and computerized systems remain in a state of permanent inspection readiness.
Key Responsibilities
- Coordinate and execute qualification of analytical instruments and equipment
- Perform Computer System Validation activities across the system lifecycle (SDLC)
- Support metrology activities including calibration planning and execution
- Manage system and equipment lifecycle activities such as upgrades maintenance and decommissioning
- Author and maintain SOPs change controls periodic reviews and validation documentation
- Support deviation investigations and CAPA activities
- Provide technical troubleshooting support for laboratory equipment
- Technical education or university degree in biotechnology analytical chemistry biochemistry IT or a related field
- Experience in Computer System Validation Commissioning & Qualification or GMP laboratory environments
- Strong documentation skills and high attention to detail
- Ability to work independently and within cross-functional teams
- Strong communication skills in German (B2) and English (B1)
- Experience with analytical instrumentation controlled temperature units audits or change management is an advantage
- Site-based role five days per week
- Limited home office possible on a need basis
- Typical working hours start between 07:00 and 08:45
- Candidates with longer notice periods will be considered
- Responsibilities can be adjusted based on experience and career ambitions
- If you are motivated by quality compliance and working close to the laboratory in a regulated environment this role offers strong development potential.
Company Industry
Pharmaceuticals
About Company
Idibu
100 employees
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