Similar posts
QC Associate Scientist
- Contract
- Good Manufacturing Practice (GMP)
- Switzerland
Proclinical is seeking a QC Associate Scientist to join our client's team in Neuchatel, Switzerland. This role focuses on managing the life cycle of analytical assays within our Quality Control Laboratories. You will be involved in laboratory investigations, critical material qualification, and laboratory method transfers. This position requires adherence to cGMP standards and EHS requirements.
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:
- Manage life cycle activities of analytical assays in QC Laboratories.
- Conduct laboratory investigations and critical material qualifications.
- Facilitate laboratory method transfers.
- Author and oversee transfer protocols and reports for assays.
- Develop qualification plans and reports for critical reagents.
- Provide training and support for validation and qualification activities.
- Investigate and troubleshoot laboratory issues, conducting risk assessments and root cause analysis.
- Own laboratory investigations and CAPA processes.
- Support compliance with industry standards and regulations.
- Participate in daily QC activities, offering technical and statistical support.
Key Skills and Requirements:
- Degree in analytical chemistry, biotechnology, biochemistry, or microbiology.
- Experience in GMP laboratory activities, preferably with recombinant therapeutic products.
- Proficiency in method transfer and critical reagent qualification.
- Strong problem solving and deviation management skills.
- Knowledge of statistical tools.
- Fluent in French and English (C1 level).
- Proficient in standard IT tools.
- Excellent collaboration and teamwork skills.
- Ability to work independently and manage multiple priorities.
- Effective communication skills and ability to synthesize information.
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.
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.
Related jobs
Highly Competitive
Visp, Schweiz
Proclinical is seeking a QA Specialist to join our client's team in Visp, Switzerland. This is a contract role.
Highly Competitive
Neuchâtel, Switzerland
Proclinical is currently working alongside a pharmaceutical company seeking a QA Expert Senior to join the QA Team.
£45000 - £50000 per annum
Windsor and Maidenhead, England
Proclinical is currently working alongside a pharmaceutical company to recruit for a QA Manager, GMP. This is a permanent position based in Surrey, UK or Lyon, France.
Highly Competitive
Visp, Schweiz
Proclinical is seeking a QA Validation Specialist PQR to join our client's team in Switzerland on a contract basis.
Highly Competitive
Visp, Switzerland
Proclinical is seeking a Quality Engineering Specialist to join our client's team in Visp, Switzerland.
Highly Competitive
Visp, Switzerland
Proclinical is seeking a QA Specialist to join our client's team on a contract basis.
Highly Competitive Salary
Philadelphia, USA
Proclinical is seeking a Senior Director of Quality Control to lead bioanalytical quality control operations for clinical and commercial cell therapy programs.
Highly Competitive
Cranbury, USA
Proclinical is currently working alongside a pharmaceutical company to recruit for a Senior Manager of Quality Assurance. This is a temporary contract position based in Cranbury, New Jersey.
US$30.00 - US$41.00 per hour
New Haven, USA
Proclinical is working alongside a pharmaceutical company seeking a QA Documentation Manager to join their growing team.