Are you ready for a change? Tired of the same routine? Join our client and make your mark in the pharmaceutical industry!
Have a look below and apply or send me your CV directly.
Quality Control Analyst - Neuchatel, Switzerland
We expect:
- You work in a structured and quality-oriented manner.
- You find satisfaction and motivation in routine tasks.
- You have experience of good manufacturing practice (cGMP).
Our client prefers a relaxed, local environment. You work in a team where tasks change very quickly. We therefore expect you to be motivated by a fast-changing environment while being able to deliver high-level results.
Main tasks:
- Produce solutions for the various QC Analytical analyses
- Potentially carry out biochemical and HPLC analysis and supervision activities in accordance with the procedures in force in the laboratory, complying with GMP/BPD rules and/or projects in connection with the activities of the Quality Control department.
- Comply with all procedures in force
- Respect and apply EHS rules.
- Complete the various forms, logbooks and documents in compliance with Good Manufacturing and Documentation Practices and ALCOA +.
- Notify the Supervisor of any non-compliant and/or invalid results on the same day, orally and/or in writing, and initiate the event in the quality system within the required timeframe.
- Manage laboratory investigations.
- Applying planning requests and reporting any concerns proactively.
- Carry out reagent/consumable qualification and validation protocols (method, system, equipment)
- Ensure that calibration and maintenance of equipment is in order at the time of analysis
- Comply with Kanban management in real time
- Report deviations from the procedure to the method/equipment manager and the Supervisor/Delegate/Expert
- Be capable of identifying and resolving certain less complex problems relating to his/her area of expertise (troubleshooting)
- Carry out or approve solutions in the laboratory.
- Manage and tidy up the laboratory in general, complying with 5S standardisation norms.
- Supporting continuous improvement initiatives
Profile required:
- Minimum level of education: CFC laboratory/biology or other relevant scientific field.
- Experience in HPLC/Elisa is a plus.
- Fluent French and technical English
- Swiss or EU nationality, or valid Swiss work permit
If you are having difficulty in applying or if you have any questions, please contact Ashley Bennett at a.bennett@proclinical.com.
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
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