Project management support állások, munkák egészségügy, gyógyszeripar területen

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...

• Lead our M&S operations & teams located in both Budapest & Barcelona Hubs
• Work in collaboration with M&S Global leadership, functions for Quality, Quality Control, Supply Chain, MSAT, HSE, Engineering, GDPU etc., subject matter experts and other hub location teams.

• Support the SolidarMed Programme Team with project management backstopping, as well as cross cutting coordination, events management, and stakeholder management
• Screen for calls for funding options, analyse eligibility, coordinate and actively support the development of new proposals/submissions

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

End-to-End Project Management: Lead CMC development programs from initiation to execution, maintaining operational and financial control through detailed plans, timelines, budgets, milestones, dashboards, and forecasts....

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

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...

• 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 complex, data-driven engagements with international healthcare stakeholders
• Design and own project frameworks, KPI models, scoring methodologies, and implementation roadmaps in close collaboration with the Analysis and Data Science teams

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

Collaborating across Kerry's global and cross-functional network to anticipate market trends, understand customer needs, and drive innovative biotechnology solutions that deliver exceptional taste, nutrition, and functionality to the food & beverage industry....

POSITION DESCRIPTION We are seeking an experienced and motivated professional to join our software quality assurance team. In this key role, you will help ensure compliance with IVDR, FDA 21 CFR Part 820, and cybersecurity requirements for medical device software. - Partner with development teams...

• Develop and implement global regulatory pathways for product authorizations
• Oversee preparation and submission of regulatory documents to authorities

Framework and Content: Develop and maintain global sales capability frameworks, designing high-impact training content (in partnership with external vendors when necessary) focused on product knowledge, clinical confidence, and compliant HCP engagement in the aesthetic space....

Scientific & Strategic Leadership: Drive the overall scientific strategy & implementation, support study protocol development, ensure GCP and research quality, and serve as scientific spokesperson to authorities and partners. You will oversee planning and control of finances, timelines,...

• Regulatory assessment of raw materials, recipes and nutrient profiles
• Creation and updating of regulatory documentation (e.g. list of ingredients, nutrition information, raw material information)
• Review and approval of labels and communication materials in accordance with EU food law

• Lead and manage client relationships for pharma and biotech accounts, ensuring satisfaction and longterm partnerships
• Serve as product owner or strategic advisor on key market access projects (AMNOG, EU HTA, pricing, reimbursement)

Development of product strategies for existing and new portfolios, including market research to identify innovation opportunities in lens technology and design, as well as defining product specifications and managing the product lifecycle...