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p>or our client, an international company based in Neuchâtel, we are looking for a QA Senior Expert.
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Start date: ASAPEnd date: 31.12.2025Extension: possible, to be discussedWorkplace: NeuchâtelWorkload: 100%
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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.
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At least 7 years of experience in an GMP environmentUniversity degree in Engineering, Biotechnology, Pharmacy or Quality Management applied to industrial process or equivalent experience in pharmaceutical and /or biotechnological companiesFluent French and a good command of EnglishDemonstrate the company Values of Integrity, Fairness, Honesty, Perserverence as a natural way of workingGood knowledge of FDA, EMA, ICH regulations, Pharmacopeias and Quality system standardsKnowledgeable in auditing and inspection against regulatory / Quality standardsKnowledge/Experience with Quality tools such as TrackwiseGood analytical skills and ability to simplify the complexSolution oriented and team spiritGood listener and communication skillsGood organizational skills and continuous improvement mindset