Overview Ready to validate the future of pharmaceutical innovation?
Duration: 6 months
Type: Temporary position
Salary: CHF 8900 monthly gross
About Our Client
For our client, a leading global pharmaceutical and life sciences company with a strong presence in Switzerland, we are seeking a skilled professional. This innovative organization is renowned for developing breakthrough therapies and maintaining world-class research and development facilities that set industry standards in analytical sciences and quality assurance.
Your Responsibilities
Oversee qualification processes for analytical instrumentation and computer systems within a regulated GMP laboratory environment
Execute system validation activities following SDLC (Software Development Life Cycle) methodologies in close collaboration with IT and site validation teams
Coordinate equipment lifecycle management, including procurement, installation, maintenance, upgrades, and decommissioning of laboratory instruments
Manage analytical metrology programs by scheduling and coordinating calibration maintenance services according to documented timelines and business requirements
Develop and maintain technical documentation, including SOPs, change controls, and periodic review documents for equipment and systems
Conduct initial troubleshooting and provide technical support for analytical laboratory instrumentation issues
Monitor and evaluate alarms from controlled-temperature units such as stability chambers and other critical laboratory equipment
Support deviation investigations and participate in CAPA management processes to ensure continuous improvement
Your Profile
Technical education (apprenticeship) in biotech, pharmaceutical industry, IT, or related fields, OR a university degree in analytical chemistry, biotechnology, biochemistry, or similar disciplines
Proven experience in Computer System Validation (CSV) or Commissioning/Qualification activities
Strong communication skills in English (B1 level) and German (B2 level), both written and oral
Excellent documentation abilities with meticulous attention to detail when creating technical documents
Independent working style combined with strong teamwork capabilities in cross-functional, dynamic environments
GMP laboratory experience and familiarity with pharmaceutical quality standards are highly advantageous
Knowledge of Change Management principles, deviation handling, and CAPA processes is a plus
Technical affinity for equipment maintenance and IT-related software systems
Benefits with Nemensis
Nemensis AG is your specialized personnel recruiter in the Life Sciences sector with headquarters in Basel
Comprehensive consultation and support throughout the application process by our consultants
Access to a large customer network and exciting positions in Northwestern Switzerland
Fast and uncomplicated entry through individual guidance and consultation in the application process
Let's Connect!
At nemensis ag, we've already connected thousands of candidates with their dream jobs, giving them the opportunity to develop further or re-enter the job market. What can we do for you and your career today? Get in touch with us!
Are you ready to take on this exciting challenge as a Computer System Validation Engineer (m/w/d) in Schachen ? We look forward to receiving your application!
You're looking for a change of perspective, but this isn't the right position for you? Then register with us – we'll contact you for an initial meeting to understand your wishes and needs and align ourselves accordingly.
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