Similar posts
Quality Assurance Associate
- Contract
- Good Clinical Practice (GCP)
- Switzerland
This vacancy has now expired. Please see similar roles below...
A worldwide biotechnology company situated in Switzerland and operating in over 70 markets worldwide is looking for a Quality Assurance Associate. The company specialises in neurological conditions and puts a great emphasis on teamwork and delivering biological products.
Job Responsibilities:
- Managing the QA interface with manufacturing and testing partners for assigned products/projects by ensuring the quality of product/process transfers, validations, tracking and resolution in a timely manner of investigations.
- Evaluating the general performance of contractors and the identification, negotiation, implementation and follow-up of process and systems improvements.
- Quality management of the product lifecycle management in relation with contract manufacturing, artworks and support to asset functions such as review and approval of regulatory filings.
Skill and Requirements:
- Minimum Bachelor's degree, Master degree preferred, in a scientific topic (Pharmacy, Chemistry, Biology, Biochemistry etc.)
- A minimum of 6 years of experience in similar position in pharmaceutical or biotechnology industries.
- Relevant experience in either manufacturing, development, quality or regulatory.
- Understanding of cGXPs, quality systems and regulations (FDA and EU, knowledge of Japanese or other geographies' regulations is a plus).
- Demonstrable multitasking, project management, and execution skills.
- Good interpersonal skills, including communication, presentation, persuasion, and influence.
- Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
- Proficiency with computer skills, such as MS Office.
To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please contact Caleb Mensah at 0203 854 1080 or upload your CV on our website - www.proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
#LI-CM3
#Compliance/Quality
Related jobs
US$65 - US$77 per hour
New York, USA
Are you looking to make an impact with your innovation? We are working with a well-established pharmaceutical company to recruit for a manager of Global Development Quality!
Highly Competitive
Risch-Rotkreuz, Switzerland
Driving precision from sample to solution-where every biospecimen tells a story of innovation.
US$180000 - US$190000 per annum
Cambridge, USA
Ready to engineer precision in the world of biotech? Join our client's cutting-edge team and play a vital role in developing the instrumentation that powers tomorrow's breakthroughs.
US$270000.00 - US$290000.00 per annum
Cambridge, USA
Are you ready to make a groundbreaking impact in the world of biotechnology? Join a growing company that's shaping the future of healthcare and science.
Highly Competitive Salary
Basel, Switzerland
Proclinical is seeking a Supplier Lifecycle Management Specialist to support global vendor change notifications and ensure seamless coordination across multiple sites.