Role DescriptionAs the Quality Assurance Manager you will be responsible for maintaining the high quality standards at external manufacturing sites, which have to meet the GMP standards. You will be responsible for the compliance of the SOP and regulatory. Within this function you will be the POC for various team members and responsible for their results. You will be the designated person to make sure that the performance of the team live up to the standards and regulations and make adjustments where necessary.
Responsibilities- Managing and coaching of the manufacturing site - Setting up and monitoring of the KPI's - Ensuring the quality of audits and batch reviews - Managing the quality of the end products according to the GMP standards - Managing the manufacturing activities according the SOP - Conducting risks assessments and managing complications - Responsible for the product acquisitions - Review of quality documents
Requirements- A Life Sciences BSc. - At least 7 years of experience within the pharmaceutical industry, preferably in the QA - At least 4 years of experience as a manager or team leader - Knowledge of the current GMP standards - Capable of risk assessment and compliance management - Fluent English communication - Assertive and result-oriented institution
Other informationIf you meet the above requirements and are motivated to work in a dedicated team with a challenging function, please let us know!
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Ria Bos.