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QA/QC Specialist

Job Field:
Regulatory and Drug Safety Jobs
QA Jobs
Switzerland All
Contract Type:
Temp / Locum / Contract
40 to 45 per hour
Key People
Job Ref:

An excellent opportunity has arisen to join a leading pharmaceutical company as a QA/QC Specialist.

- Document management in iRelease (GMP database)
- Document management in Doc Store VIPER (GMP database)
- Archiving of TRD QA OPeration GMP paper documents
- Scanning of documents
- Administrative support: Due Date Tracking, Trending, Communication
- Review and compile GMP documents

Must have skills:
* English is a must, German or French is a plus
* Being comfortable with IT Systems

Soft skills:
* Able to work in a team
* Good communication and contact skills to allow collaboration with different stakeholders
* Rigorous
* Detail-oriented
* Well organised
* Precise, attention to details

Key People is a specialist international recruitment consultancy with over 25 years' experience of working within the life sciences, biotech, healthcare and CRO industries. Our experienced and dedicated clinical research related consultants have a long history of success, excellent technical knowledge and a flexible, consultative focussed approach to recruitment.

Please contact Mark Cussens, Clinical Research Recruiter on
Tel: +44 1727 817623 or email:
Tel: +41 4350 86620 or email:

Key People is a recruitment company with a reputation for providing good value that's been built up over 20 years.
-We achieve results faster
-Our candidates really are a cut above
-We add greater value
We think it's because we're a private company driven by clients, not by shareholders.

For our candidates, we have developed relationships with thousands of clients nationwide and across Europe, who choose to recruit through Key People, so you'll have a wide choice of opportunities to further your career.

Closing Date:

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