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    • Remove Selection Biotechnologie/ Pharma/ Medizinaltechnik
      • Remove Selection Adjoint e du responsable du c for 100
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                  Adjoint e du responsable du c for 100-Jobs als Freie Mitarbeit, Dienstvertrag, Projekt-Stelle in der Branche Biotechnologie, Pharma, Medizinaltechnik

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                  MBA - Basel, Basel Stadt(Seit 4 Tagen)
                  For our Global Pharmaceutical Client we are recruiting for a Clinical Documentation Compliance Manager who will oversee the adherence and compliance of TMF data according to Global Clinical Regulations. This position sits within the Clinical Document Governance and Management team and reports to the TMF Operational Excellent Head. Responsibilities: Responsible for monitoring of TMF process complia...
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                  MBA - Zug, Aargau(Seit 27 Tagen)
                  We have an urgent project for a quality consultant to support deployment and implementation of projects defined under implementation of the new regulation for the medical devices. Major Responsibilities: Collaborate with Regulatory department in order to collect the data from the dossiers in regards of the medical devices (for combination products) Collaborate with internal stakeholders (Source QA...
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                  MBA - Solothurn, Solothurn(Seit 3 Tagen)
                  Specialist Associate Supplier Quality Engineer is needed to support remediation project with regards to new MDR regulations. Requirements: Management supplier's related Non-Conformities (NC's).Ensuring timeline of NC closure and adequacy of corrective action as well as audit proof documentation Management of supplier's related Corrective and Preventive Actions (CAPA's) Management of supplier's cha...
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                  MBA - Solothurn, Solothurn(Seit 3 Tagen)
                  We are searching for a quality engineer to join a remediation project to support compliance with EU MDR requirements. Your role will involve collaboration with suppliers to obtain details for manufacturing process information, production risk, management processes. RESPONSIBILITIES: performing and supporting tasks related to the technical file remediation products to meet EU MDR requirements. meet...
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                  MBA - solothurn, Solothurn(Seit 6 Tagen)
                  We have a new opportunity for a regulatory affairs expert with prior experience in medical devices to support the team in creation and maintenance of Technical Documentation for CE marked products (implants and instruments) according to with MDR compliance framework. Tasks: Support preparation of technical documentation and develop dossier documentation for submission to and review by Notified Bod...
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                  MBA - solothurn, Solothurn(Seit 6 Tagen)
                  Global medical devices company is looking for an experienced Quality Project Manager to support MDR compliance execution work by acting as project manager for external supplier relations who has oversight on ongoing MDR compliance projects and drives completion of MDR. Tasks: - Support execution of project plan for MDR compliance business for 2019 - Lead and track completion of MDR drawing updates...
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