For our client, an international company based in Neuchâtel, we are looking for a QA Senior Expert.
General Information:
- Start date: ASAP
- End date: 1 year contract
- Extension: possible, to be discussed
- Workplace: Neuchâtel
- Workload: 100%
Tasks and responsibilities:
- Responsible for Quality Assurance in the frame of activities all along the manufacturing and release process.
- QA representative for both routine GMP activities and company projects.
- Quality partner within Production Unit Team and the Quality Control laboratories, Warehouse and Engineering/Maintenance departments as applicable.
- Ensure quality of information within systems and documentation in respect to current guidelines, compliance and regulatory requirements.
- Participation in GMP audits and shopfloor.
- Promote and be involved in Continuous Improvement.
- Understand and apply company EHS guidelines and commitments policy, take care of its own safety, report risk situations and improvement opportunities to supervisory personnel.
- Can act as back up of other QA Senior experts and QA Lead as requested.
Your profile:
- At least 7 years of experience in an GMP environment
- University degree in Engineering, Biotechnology, Pharmacy or Quality Management applied to industrial process or equivalent experience in pharmaceutical and /or biotechnological companies
- Fluent French and a good command of English
- Demonstrate the company Values of Integrity, Fairness, Honesty, Perserverence as a natural way of working
- Good knowledge of FDA, EMA, ICH regulations, Pharmacopeias and Quality system standards
- Knowledgeable in auditing and inspection against regulatory / Quality standards
- Knowledge/Experience with Quality tools such as Trackwise
- Good analytical skills and ability to simplify the complex
- Solution oriented and team spirit
- Good listener and communication skills
- Good organizational skills and continuous improvement mindset
For our client, an international company based in Neuchâtel, we are looking for a QA Senior Expert.
General Information:
- Start date: ASAP
- End date: 1 year contract
- Extension: possible, to be discussed
- Workplace: Neuchâtel
- Workload: 100%
Tasks and responsibilities:
- Responsible for Quality Assurance in the frame of activities all along the manufacturing and release process.
- QA representative for both routine GMP activities and company projects.
- Quality partner within Production Unit Team and the Quality Control laboratories, Warehouse and Engineering/Maintenance departments as applicable.
- Ensure quality of information within systems and documentation in respect to current guidelines, compliance and regulatory requirements.
- Participation in GMP audits and shopfloor.
- Promote and be involved in Continuous Improvement.
- Understand and apply company EHS guidelines and commitments policy, take care of its own safety, report risk situations and improvement opportunities to supervisory personnel.
- Can act as back up of other QA Senior experts and QA Lead as requested.
Your profile:
- At least 7 years of experience in an GMP environment
- University degree in Engineering, Biotechnology, Pharmacy or Quality Management applied to industrial process or equivalent experience in pharmaceutical and /or biotechnological companies
- Fluent French and a good command of English
- Demonstrate the company Values of Integrity, Fairness, Honesty, Perserverence as a natural way of working
- Good knowledge of FDA, EMA, ICH regulations, Pharmacopeias and Quality system standards
- Knowledgeable in auditing and inspection against regulatory / Quality standards
- Knowledge/Experience with Quality tools such as Trackwise
- Good analytical skills and ability to simplify the complex
- Solution oriented and team spirit
- Good listener and communication skills
- Good organizational skills and continuous improvement mindset
