Associate Director QC – Neuchâtel, Switzerland

BioTalent is currently supporting a leading global pharmaceutical organisation that are seeking a highly motivated and experienced Quality Control Associate Director. You will play a pivotal role in in the direct management of individual contributors, supervisors and managers.

Key Responsibilities:

• Responsible for ensuring efficient QC GMP practices.
• Accountable for all QC activities to be delivered on time to clients. This will include Raw Material testing, validation of new methods and LIMS.
• Involvement in NPI with accountability for building good relationships with clients with QC interests.
• Work closely with EHS to promote safe practices and behaviours.

Requirements:

• Extensive experience in the pharmaceutical industry, ideally in solid dosage forms.
• Extensive experience in QC and people management.
• Strong knowledge of GMP and presenting regulatory audits.
• Fluent French & English

This is an excellent opportunity to get involved in a global leader whilst working at the forefront of science with a strong culture of collaboration.