Similar posts
QC analyst
- Contract
- Good Manufacturing Practice (GMP)
- Switzerland
This vacancy has now expired. Please see similar roles below...
Proclinical is seeking a QC Analyst to join a pharmaceutical company in Neuchatel, Switzerland, on a contract basis. In this role, you will focus on performing biochemical analyses and ensuring compliance with GMP standards within a fast-paced quality control laboratory environment. This position requires a proactive and detail-oriented individual who thrives in a dynamic setting.
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:
- Conduct biochemical analyses such as ELISA, enzymatic activity assays, Western Blot, and HPLC.
- Ensure compliance with GMP, EHS, and quality control procedures.
- Document results accurately in logbooks and forms following Good Documentation Practices (ALCOA).
- Report non-conformities or invalid results promptly and initiate quality events as required.
- Manage laboratory investigations and troubleshoot minor issues within your area of expertise.
- Execute qualification protocols for reagents, consumables, methods, systems, and equipment.
- Verify calibration and maintenance of equipment before analysis.
- Maintain Kanban inventory management in real-time.
- Support continuous improvement initiatives and adhere to 5S standardization practices.
- Collaborate with supervisors and experts to address procedural deviations.
Key Skills and Requirements:
- Educational background in laboratory biology (CFC) or a relevant scientific field.
- Experience in a QC laboratory within a cGMP environment.
- Proficiency in techniques such as electrophoresis, HPLC, ELISA, or enzymatic activity determination.
- Fluency in French and technical proficiency in English.
- Swiss or EU nationality, or a 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.
Apply Now:
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.
By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.proclinical.com/privacy-policy
Related jobs
Highly Competitive
Brussels, Belgium
Our client is on the search for a Qualified Person to play a key role in maintaining top-tier quality standards!
Highly Competitive
Thousand Oaks, USA
Advance quality excellence by driving analytical method transfer and validation in a cGMP environment.
Highly Competitive
Visp, Switzerland
Join our QC Bio-Chemie team and turn precision into impact as a Lab Technician in Switzerland.
Highly Competitive
Neuchâtel, Switzerland
Ensure the highest quality standards in pharma by leading critical lab analyses and driving continuous GMP excellence.
Highly Competitive
Chertsey, England
Drive GMP excellence and shape quality systems that support life‑changing rare disease therapies.
US$100000 - US$120000 per annum
New Hampshire, USA
Are you passionate about quality and precision? Join our client as Director of Quality and help ensure top-tier standards every day.
Highly Competitive
Amsterdam, Nederland
Safeguarding clinical quality through precision, compliance, and unwavering attention to detail.
US$20 - US$23 per hour + Highly Competitive Salary
Philadelphia, USA
Proclinical is seeking an Inventory Control Specialist to support inventory accuracy and integrity within a facility.
Highly Competitive
Philadelphia, USA
Drive the quality systems that keep GMP operations compliant, efficient, and audit‑ready.
Highly Competitive
Philadelphia, USA
Ensure GMP excellence by owning the accuracy, integrity, and compliance of critical quality documentation.