Location: Breda
Duration: 1 year (extension may be possible)
Language: English/Dutch is a plus
Industry: Biotechnology
Start date: 02/01/2023

The company
Our client is an innovative leader on the field of pharmaceutical biotechnology. Over the past 40 years, they have been pioneers in developing revolutionary medicine to help ill people around the world.

About the role
As a Quality Assurance Specialist you will act as first point of contact for quality related matters and support the production staff in regards to compliance with Standard Operations Procedures and GMP.

Responsibilities
-Review SOP's, Work Instructions and deviations records
-Review and approve batch production record data
-Assist in ABR projects
-Own and maintain performance boards
-Perform GMP compliance checks in production

Requirements
-MBO or Bachelor's degree in Life Sciences or related
-minimum 2 years of working experience as a QA or manufacturing or medical devices industry
-GMP, GDP or GCP knowledge

Additional information
-Ability to work in shifts (2 morning & 1 night shift)

Ready for the next step in your career? Do not hesitate to apply