Key Responsibilities: • Provide strategic guidance on regulatory requirements and submissions, first in Switzerland, but later also in the EU • Actively manage relationships with
January 22, 2025
Key Responsibilities: • Provide strategic guidance on regulatory requirements and submissions, first in Switzerland, but later also in the EU • Actively manage relationships with
Senior Scientist Process and Formulation Development for Oral Solid Dosage Forms
Key responsibilities: Lead and coordinate pre-formulation, formulation and process development tasks and represent pharmaceutical development in the project team Accountable for managing all pharmaceutical development
Account Manager Formulated Chemistry Switzerland
Key responsibilities: Sell and support the use of cleaning agents, disinfectants and biological & chemical indicators to prove these processes are in tight control. Sell
Principal Scientist in Pharmaceutical Development – Oral Solid Dosage Forms
Key responsibilities: Lead and coordinate pre-formulation, formulation and process development tasks and represent pharmaceutical development in the project team Accountable for managing all pharmaceutical development
Key responsibilities: Lead and coordinate pre-formulation, formulation and process development tasks and represent pharmaceutical development in the project team Accountable for managing all pharmaceutical development
Global Project Leader Oncology
Key responsibilities: Guide innovation, provide drug development expertise and strategic leadership to the Programs and project teams, comprising all pre-clinical, clinical, technical, regulatory, operational and
Recruitment Manager Digital Healthcare
Key responsibilities: Following clearly defined briefs from our clients, your focus is to drive diligent filtering of applications, reviewing CVs, vetting candidates, interviewing and evaluating
Lead the development and implementation of the site R&D strategy including alignment with the site objectives and Global R&D.
Responsibility for leading the development, scale-up, registration/validation of drug substance, particle engineering and drug development programs for the site.
Fellow Scientist – Bioavailability
Actively contributes to the development and implementation of company’s strategy for the area and the standardization of best practices. Supervise projects within the area, proving technical expertise and best practices to the area TMs and ensuring the right networks are developed, internally and externally…
Fellow Scientist – Continuous tableting
As Subject matter expert, you will be responsible for the technical strategic programme in the field of continuous tableting. Responsible for portfolio of projects within the programme, from ideation to launch including prioritisation, governance, resourcing and overall budget management
The Execruit team brings an unparalleled expertise and passion to address your talent recruitment, leadership assessment and development, career development, outplacement and e-learning requirements.