For our client, an international company based in Neuchâtel, we are looking for a QA Senior Expert. General Information:Start date: 01.01.2025End date: 31.07.2025Workplace: NeuchâtelWorkload: 100% Tasks and responsibilities:Responsible for Quality Assurance in the frame of activities all along the manufacturing and release process.Responsible for compliance and quality oversight related to activities throughout the manufacturing and release process of bulk
For our client, an international company based in Neuchâtel, we are looking for a QA Senior Expert. General Information:Start date: 01.01.2025End date: 31.07.2025Workplace: NeuchâtelWorkload: 100% Tasks and responsibilities:Responsible for Quality Assurance in the frame of activities all along the manufacturing and release process.Responsible for compliance and quality oversight related to activities throughout the manufacturing and release process of bulk
Are you an experienced Senior Manager within Regulatory Sciences? Do you have experience within a Pharmaceutical or Biotechnology setting? If so, we would love to hear from you! The successful candidate will support multiple EU leads by contributing to the development and implementation of EU regional clinical and pre-clinical regulatory strategy for products pre or post MAA approval, in alignment with the EU business strategy. This is a contract positi
Are you an experienced Senior Manager within Regulatory Sciences? Do you have experience within a Pharmaceutical or Biotechnology setting? If so, we would love to hear from you! The successful candidate will support multiple EU leads by contributing to the development and implementation of EU regional clinical and pre-clinical regulatory strategy for products pre or post MAA approval, in alignment with the EU business strategy. This is a contract positi
ResponsibilitiesPerform and document daily tests on incoming/outgoing waste, water, and oil, ensuring results are accurate and reported.Conduct in-process testing to ensure product conformity and meet operational standards.Record and reconcile product stock figures, addressing issues proactively with relevant departments.Maintain and update EPA waste license records, promptly reporting any non-conformities.Follow health and safety policies, conducting risk
ResponsibilitiesPerform and document daily tests on incoming/outgoing waste, water, and oil, ensuring results are accurate and reported.Conduct in-process testing to ensure product conformity and meet operational standards.Record and reconcile product stock figures, addressing issues proactively with relevant departments.Maintain and update EPA waste license records, promptly reporting any non-conformities.Follow health and safety policies, conducting risk
For our client Merck in Aubonne, we are looking for a QA Specialist for QC (m/f/d) for a period of 12 months.Your role: To ensure the quality oversight and compliance of QC activities and the data integrity of QC analytical data in timely manner. QA Oversight on QC analytical data:To perform the QA review on QC analytical data, on QC documentation. Manage QC deviation, CCP and CAPA as QA.Compliance of QC activities:QA support for QC activities including ne
For our client Merck in Aubonne, we are looking for a QA Specialist for QC (m/f/d) for a period of 12 months.Your role: To ensure the quality oversight and compliance of QC activities and the data integrity of QC analytical data in timely manner. QA Oversight on QC analytical data:To perform the QA review on QC analytical data, on QC documentation. Manage QC deviation, CCP and CAPA as QA.Compliance of QC activities:QA support for QC activities including ne