Software developer m f d állások, munkák egészségügy, gyógyszeripar területen

Új szilárd gyógyszerkészítmények, kísérleti tervek elkészítése, kísérletek elvégzése, kiértékelése. Valamint a forgalomban lévő készítmények piacon tartásával kapcsolatos technológiai feladatok elvégzése....

• In vitro farmakológiai, sejtbiológiai kísérletek elvégzése
• Műszeres mérések kivitelezése, laborműszerek, elsősorban automatizált patch clamp műszer kezelése, vezérlése
• A kísérletes munka dokumentálása

Design and execute strategic, customer-centric initiatives, including high-profile Investigator Meetings and site engagement activities, to align with our global development goals....

• Product Management for electric-acoustic solutions and related objective measures
• End-to-end product lifestyle management: from requirements gathering and development support to launch activities and in-life management
• Delivery of presentations and training for employees, professionals, and recipients

• Market development in alignment with the Commercial Operations team
• Developing and conducting product trainings (online and classroom)
• Participation in product launch activities
• Answering questions from the local sales and service organizations
• Support on customer visits, exhibitions and congresses

• Conduct studies on extractables and leachables from medical devices, including evaluation, interpretation, and documentation of results
• Identify and characterize potential extractables and leachables using internal and external databases

• Leading a high-performing team of analysts and the Country CFC Insights Lead
• Developing and implementing performance measurement, forecasting models, and omnichannel strategies
• Collaborating closely with Finance, Digital, CMO, and other cross-functional teams

• Planning and initiation of business cases, definition of the project scope, objectives and deliverables. This includes gathering requirements, assessing feasibility and developing a project plan that aligns with organizational goals
• Monitoring of timelines and budget

• Ramp up the practice together with the German holding company
• Comprehensive patient care including anamnesis, diagnostics and surgical planning
• Independent performance of liposuctions and surgical reconstructions after thorough training in our surgical home base Munich (Germany)

Point of contact for Regulatory Affairs colleagues with focus on Latin America regarding product registrations, including guidance on responding to deficiency letters and regulatory authority inquiries...

PHARMACOEPIDEMIOLOGIST (M/F/D)- RWD/ EPIDEMIOLOGICAL/ PHARMACOEPIDEMIOLOGIC/ CLINICAL TRAILS/ BIOMARKER/ INSURANCE CLAIMS/ EHR/ MEDICAL/ MEDDRA/ SNOMED/ ICD 10/ CPT/ HCPCS/ R/ PYTHON/ SQL/ DATA VISUALIZATIONS/ R SHINY/ R MARKDOWM/ STATISTICAL ANALYSIS/ ENGLISH PROJECT: For our customer a big...

Provide strategic statistical consultation and hands-on implementation of advanced methodologies to optimize clinical trial designs and data analytics;...

as part of DFG sponsored project beginning in January 2026 limited for three years. The Title of the project is: EFFECTS OF LACTOBACILLUS REUTERI DSM 17938 ON THE ACUTE PSYCHOLOGICAL, ENDOCRINE AND IMMUNOLOGICAL STRESS RESPONSE IN HEALTHY CITY DWELLERS. Both preclinical and clinical data support...

• 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

• Ensuring process adherence for the pre-market procedures
• Completeness of design history files and regulatory submissions
• Regulatory and process conformance for development and maintenance projects as a member of cross-functional teams

Serve as the medical device subject matter expert to both internal and external customers for product development, risk assessment, training, implementation, literature reviews, complaints, safety signals, field action, voice of the customer, and voice of the business....

Lakók mentális gondozása képesség, készségfejlesztés szabadidő szervezés életviteli segítségnyújtás...

• Develop and validate LC-MS methods for the quantification of impurities in complex samples
• Optimize and troubleshoot analytical methods to ensure accuracy, precision and robustness 
• Collaborate closely with cross-functional teams to drive project success

• 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

• Drive regulatory strategy for new product launches, ensuring proactive and effective planning aligned with global requirements
• Lead a team of regulatory experts in External Devices & Software within Regulatory Affairs