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QA specialist
- Contract
- Good Manufacturing Practice (GMP)
- Switzerland
À±½·ÊÓƵ is seeking a QA Specialist to join our client's team on a contract basis. This role focuses on managing and executing Quality System-related projects, ensuring alignment with organizational and regulatory standards. We are looking for someone who can effectively collaborate with cross-functional teams and contribute to drafting and reviewing procedures.
Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.
Responsibilities:
- Collaborate with cross-functional teams to manage and execute Quality System-related projects within defined timelines
- Drafting, reviewing, and finalizing new procedures to ensure clarity, consistency, and alignment with organizational and regulatory requirements
Key Skills and Requirements:
- Bachelor (B.Sc.) or Master (M.SC.) in natural sciences or related field
- Significant work experience in a GMP regulated environment, preferably within a Quality System unit
- Ability to interact with several stakeholders and handle multiple tasks simultaneously
- Very good knowledge of written and spoken English; German as an advantage
- Proficiency with Microsoft tools - especially Excel and Power Point
If you are having difficulty in applying or if you have any questions, please contact Emile De Beer at e.debeer@proclinical.com
Apply Now:
If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.
À±½·ÊÓƵ is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. À±½·ÊÓƵ is acting as an Employment Agency in relation to this vacancy.
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