Role DescriptionAs QA Manager you are responsible for verifying that batches meet the statutory GMP requirements of the countries where the products are headed for (including EU / USA and Brazil) and the applicable customer agreements. The QP will be responsible for certifying the approved batches. You Support the Quality Head in maintaining and improving the quality standards at various sites in Belgium, resulting in compliance with legal and customer requirements. Finally, you advise how GDP and GMP regulations and customer requirements can be translated into processes, procedures and instructions.
Responsibilities- You manage the department in general in terms of organizational, personnel matters, and ensure an effective and efficient department with optimal working conditions; - You undertake selection, performance and assessment interviews, guide and advise employees regarding their development, in collaboration with the staff development plans for them; - You Ensure effective communication within the department through work meetings and other means of communication, so that employees are up to date, informed and involved; - You participate in risk assessments and in the implementation of changes (both operational and systematic); - You act as the back up for the Quality Manager in respect of the responsibility for the Quality Systems.
Requirements- Wide experience in the pharmaceutical sector, which at least several years in a QA role; - People management skills; - Experience in the field of auditing and supervision of inspections; - Ability to translate legislation into practical significance; - Affinity with commercial and business aspects; - Excellent communication skills, able to act diplomatically; - Fluent in French and English.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees Roffelsen.