Role DescriptionFrom a QA perspective you are responsible for Equipment, Automation and IS Validation.
Responsibilities- Perform review and approval of equipment and automation validation documentation, ensuring that Corporate, Site and Regulatory requirements are met. - Keeps quality oversight on validation strategy and deliverables for specific projects. - Maintain a close contact and familiarity with Quality systems. - Provide guidance and direction to Quality, Production, Warehouse/Distribution and Supply Chain staff in regards to compliance with quality policies, standards and procedures.
Requirements- Degree in Life Sciences - Relevant experience in GMP environment - Experience in QA and manufacturing/packaging environment - English Language skills
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Daniel Woudenberg.