Senior python developer állások Svájcban (minőségbiztosítás)

EINFÜHRUNG We offer an exceptional opportunity for a professional seeking a challenging role in a renowned, fast-growing pharmaceutical company. Our client operates at the forefront of drug safety and pharmacovigilance, delivering high-quality scientific insights to support patient-focused risk...

SENIOR DATA SCIENTIST - LITERATURE (M/F/D)-INFORMATION SCIENCE/ PHARMACEUTICAL/ RESEARCH/ DEVELOPMENT/ PHARMACOVIGILANCE/ MEDICAL/ DRUG/ BIOMEDICAL/ SYNTHESIZE SCIENTIFIC DATA/ COMPETITOR INFORMATION ACCESS PLATFORM/ DIALOG/ ENGLISH PROJECT: For our pharmaceutical customer based in Basel, we are...

• Management of deviations, change requests as well as corrective actions and preventive actions
• Review of equipment qualifications, batch documentation, and product release preparations for clinical studies

TECHNICAL R&D ASSOCIATE SCIENTIST (M/F/D)- ANALYTICAL INSTRUMENTATION/ HPLC/ MS/ LC-MS/ OLIGONUCLEOTIDES/ ENGLISH PROJECT: For our pharmaceutical customer based in Basel, we are looking for a Technical R&D Associate Scientist (m/f/d) BACKGROUND: Behind each product in clinical trials or sold by...

• Start Date:or
• Latest Possible Start:
• Duration: 6 months initially; extension possible (e.g., additional 6 months)
• Location: Basel
• Workload: 100%
• Home Office: Yes
• Travel: Not expected
• Team Size: PCS safety team approx. 6; cross-functional project teamsmembers
• Hiring Manager: Simone Melega

Training Schedule Coordination: Collaborate with the Program Lead to define and maintain the annual training schedule....

• Responsible for processing incoming complaints in accordance with applicable process specifications
• Independent processing and assessment of complex or critical complaint cases with potentially high risk to patient safety or regulatory compliance

• Design, develop, and optimize coagulation diagnostic assays and reagents
• Lead feasibility studies, verification, and validation activities in compliance with ISOand IVDR requirements
• Document all activities according to quality system procedures and design control standards

• Developing and maintaining sterility assurance and contamination control strategies for aseptic processing
• Leading risk assessments for aseptic process, single use systems and critical interventions, and ensuring compliance with authorities relevant Guidance such as Annex 1