20.09.24 | Vollzeit | Corsier-sur-Vevey | Randstad Schweiz AGAnd/or approve qualification/validation documents, risk assessment, SOPs and take quality decisions according to company standards The activities of the QA Expert cover all qualification/validation phases from Basic Design until 1st use of equipment/raw material.10. You ensure GMP compliance during all phases
Später ansehen19.09.24 | Vollzeit | Corsier-sur-Vevey | Randstad Schweiz AGAnd reporting, to ensure the delivery of our specialty innovator Biotech pipeline to patients. Your Rôle - Contribute to the startup of high-tech analytical laboratories in the BDC by supporting procedure/document writing and analytical equipment for at least one of the following areas (e.g., for liquid
Später ansehen19.09.24 | Vollzeit | Vaud | Randstad Schweiz AGThe analytical CMC sections of regulatory submissions from source documents, ensuring cGMP compliance and data integrity in alignment with the company's quality standards. Collaborate with CROs and CMOs to ensure the analytical life cycle management and secure supply of licensed products, meeting the approved
Später ansehen17.09.24 | Vollzeit | Aubonne | Randstad Schweiz AGTo ensure appropriate documentation and data management using corresponding IT system, including QMS softwares (TrackWise, ManGo), ERP (SAP), Discoverant… - Assure the timely delivery of required documents (plans, protocols and reports…) as defined in the project plan - Ensure that all process support
Später ansehen09.09.24 | Vollzeit | Corsier-sur-Vevey | Randstad Schweiz AGAnd documentation of project activities as required. Your Profile - Strong knowledge in biotechnological processes, detailed manufacturing operations (including automated & execution systems, engineering designs, P&ID, etc.), and new technologies. - Pragmatic, solution-oriented, and resilient with the ability
Später ansehen30.08.24 | Vollzeit | Montreux | Randstad Schweiz AGKey responsibilities will include - Providing patient care in accordance with established protocols and procedures. - Communicating effectively with patients, families, and healthcare teams. - Documenting patient care services accurately and timely. - Adhering to the highest standards of medical
Später ansehen26.08.24 | Vollzeit | Corsier-sur-Vevey | Randstad Schweiz AGSampling, aliquoting, utility sampling, HVAC, Gases, corrections of working papers, ) - Perform support activities (autoclave and part washer) - Carrying out the documentation related to your function (e.g. writing working instructions) - Supporting compliance activities (batch review, deviations
Später ansehen23.08.24 | Vollzeit | Corsier-sur-Vevey | Randstad Schweiz AGPractices, registration product files and site quality standards. - To ensure that the documentation linked to the validation is done according to defined planning to support the establishment of the APR for the commercial and clinical molecule. - To highlight the potential project's issue from a pro-active
Später ansehen07.08.24 | Vollzeit | Aubonne | Randstad Schweiz AGAnd documentation skills · Excellent communication and interpersonal abilities for collaborating with cross-functional teams · Familiarity with software development life cycles and quality assurance practices · SAP S/4 HANA (or different version) experience needed Preferred Qualifications · Experience
Später ansehen15.07.24 | Vollzeit | Aubonne | Randstad Schweiz AGAnalytical 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 new guidelines, new pharmacopeias versions. Support the implementation of all QC projects. To perform Quality
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