Technical marketing manager állások, munkák egészségügy, gyógyszeripar területen

• Literature reviews as requested by client epidemiologists using the best practice methodologies
• Literature search and preparation of Literature review report for Pharmacoepidemiology
• Perform peer Scientific & Technical Review

• Execution of validation and testing activities according to quality requirements
• Validation and qualification of manufacturing and testing equipment
• Supporting the preparation of validation protocols, reports, and maintenance procedures
• Identifying and documenting potential process or equipment gaps

• Verify that parameters, op. conditions and acceptance criteria are defined (per SOP)
• Collect electronically stored data (e.g., from suppliers)
• Describe project details
• Ensure data integrity and adherence to quality rules are regulations

• Acquiring and maintaining parallel trading licenses (dossier updates and submissions).
• Preparing packaging materials (artwork files, mock-ups, and other graphic materials).
• Preparing and maintaining the item list.

For each assigned therapeutic project (synthetic or biologic molecule) and once agreed with the CMC Project Team actors, the CMC OPCM is the single accountable person for the accuracy of the entered plan and regularly updated in the planning tool (Planisware solution). The CMC OPCM ensures that the...

Once agreed upon with CSO Project Team actors (3-6months ahead of M2), the OPCM CSO is the single accountable person for the accuracy of the entered plan and regular updates in the planning tool (Planisware solution). The OPCM CSO ensures that the clinical operational plan reflects the project...

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...

• Kennenlernen des vollumfänglichen Herstellungsprozesses eines Medikaments – von der Rohstoffverarbeitung bis zur Verpackung
• Arbeiten in einer der modernsten Produktionsanlagen Europas für Arzneimittel
• Begleitung durch erfahrene Teams, die ihr Know-how in der Herstellung fester Arzneiformen weitergeben

Lead and coordinate the Site-Launch activities and associated teams for internal and external sites and development projects...

Algorithm Design & Prototyping: Design, develop, and validate predictive and analytical algorithms for CGM data. Develop robust code using advanced ML and statistical techniques to prove technical feasibility....

• Execute test protocols in laboratory environment. 
• Report test results and nonconformities in a timely manner. Stock management and delivery. 
• Support the follow-up and documentation of stock moves (e.g., inventory check).
• Support the preparation of delivery orders. Laboratory equipment management.

• Oversee work for timely completion of a complaint investigation and response to the various customers
• Communicate with customers regarding complaints, product issues and returned devices

• Lead and support cross-functional projects in regulatory affairs and quality management.
• Identify, interpret, and implement regulatory requirements across global markets, with a strong focus on international registrations outside the U.S. and EU.

EINFÜHRUNG We offer an exceptional opportunity for a professional seeking a challenging and impactful role in a fast-growing healthcare technology company. Our client is at the forefront of medical device innovation, focusing on Continuous Glucose Monitoring (CGM) systems that transform patient...

• Manage and validate embedded computerized systems integrated into industrial equipment.
• Execute validation activities specifically related to embedded systems, in compliance with applicable regulations and internal procedures.

Lead material selection process (evaluation, recommendation, and decision) in the different stages of the innovation process (discovery, development, and post-market)....

• design hard- and software solutions to address intraoperative workflow problems of surgeons
• gather and integrate customer feedback to refine your designs
• build proof-of-concept demonstrators and test your solutions with product management and clinical partners

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

• Ensure economic success of ZEISS Microsurgery Visualization Systems by identifying customer needs, defining product strategy, and creating new business models
• Manage the full product lifecycle, balancing customer needs, technical feasibility, and economic constraints to determine what gets built.

• 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