QA IT MES Specialist
QA IT MES Specialist
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1 Vacancy
Job Description
Joint skills in QA and IT required! French speaking job
- Join a Global Leader in Biopharmaceutical Innovation
- ASAP Initial Contract: 6 months (extension highly probable until end of 2025)
- As a QA IT MES Specialist you will be at the forefront of ensuring excellence and compliance during the implementation of an electronic batch record system. With a strong focus on Computerized System Validation (CSV) you will work alongside crossfunctional teams to uphold the highest standards of quality and compliance.
What Youll Do:
- Represent Quality in site and global project teams providing oversight and expertise on CSV and validation activities.
- Ensure all quality aspects of the project comply with Global Policies SOPs and GMP regulations.
- Review and approve key documentation including risk assessments validation protocols and configuration specifications.
- Collaborate with project teams to address quality issues organize QA activities and promote compliance with data integrity standards.
- Act as a key QA liaison ensuring seamless communication among stakeholders and supporting an agile validation approach.
What Youll Bring:
- Proven experience in Computerized System Validation (CSV) and a strong understanding of cGxPs and industry standards.
- Fluency in English and French is essential.
- Exceptional communication and organizational skills to collaborate across diverse teams.
- A proactive mindset with the flexibility and dedication to meet project timelines.
- Residency or work permit in Switzerland is mandatory (crossborder workers welcome).
Whats in it for You
- Be part of a globally renowned biopharmaceutical company.
- Collaborate on cuttingedge projects that shape the future of healthcare.
- Work in a stateoftheart facility overlooking the beautiful Lake of Neuchtel.
Employment Type
Full Time
