Key responsibilities: Audit & CAPA process owner On behalf of the Head of Quality, act as business owner for “Audit & CAPA System”: single point
August 9, 2023
INSIGHTS
Consultant Clinical Scientist Oncology (6-months full time role)
Drive development of protocols/protocol amendments for clinical studies. Prepare and/or provide input to clinical study related and other regulatory documents (e.g. CSRs, IBs, PIS/ICFs, SAPs, Data Management Plans, Safety Management Plan, Medical Monitoring Plan, SRC Charter, IND, briefing books)
July 25, 2023
Senior Clinical Development Director Oncology ( Early Development)
Provides the strategic direction and clinical development plans (definition and updates). Is a permanent member of Core team, leader of the clinical sub-team and depending on the program, may also be a member of study team…
July 18, 2023
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…
July 11, 2023
Quality Management Systems (QMS) Team Lead, (Associate) Director
Act as a strategic driver to build and implement a sustainable transversal QMS Procedural Document (ProcDoc) / Training Framework driving the day-to-day GxP development activities
Evaluate operations from a strategic level to ensure that the QMS consistently meet quality and regulatory requirements from a Procedural Document and Training perspective
June 6, 2023
Act as a strategic driver to evaluate, optimize and implement the pro-active, fit-for-purpose and risk-based Clinical Quality Strategy ensuring compliance during the day-to-day clinical drug development activities. Drive the quality culture and create quality awareness throughout the clinical development organization
June 6, 2023
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
May 23, 2023
As Subject matter expert, you will be responsible for the technical strategic programme in the field of Inhalation. Responsible for portfolio of projects within the programme, from ideation to launch including prioritisation, governance, resourcing and overall budget management
May 23, 2023
Fellow Scientist – Nutraceuticals
– Actively contributes to the development and implementation of compnay’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
May 7, 2023
Fellow Scientist – Sustainability
– 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
May 7, 2023
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Contact information
- Martinsgasse 20, CH-4051 Basel, Switzerland
- (+41) 78 889 3675
- signe.reidla@execruits.com