Role DescriptionAs QA/QP specialist you will be responsible for the daily oversight and guidance to the colleagues of the Production site to in regards with Quality Policies and Procedures. This role is for the period of one year, with the possibility of prospects for a permanent role.
Responsibilities- Disposition batches labeled and packaged - Handle Non Conformances and CAPA’s mainly as initiator or QA-contact. Lead and assist in various investigations as needed - Own, review and approve SOP’s - Handle change control records mainly as assessor or as QA contact - Partner with Production staff in performing risk analysis and the establishment of quality limits and requirements - Perform GMP compliance checks in production - Assist in development and delivery of GMP training activities for QA- and production staff
Requirements- MSc. Industrial Pharmacy ; QP qualified (Belgian regulations) - Years of experience in (bio)pharmaceutical production environment - 10+ years of related professional experience Relevant experience in dealing with Non Conformances and Change Control records - Sound knowledge of Good Manufacturing Practice and Good Distribution Practice - Customer oriented and service minded - Good problem solving skills
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Laura Hoekstra.