Role DescriptionAs QA specialist (with emphasis on validation), you will be the bridge between quality and engineering to ensure new equipment is introduced within manufacturing conforming quality guidelines.
Responsibilities+ Agree on the validation strategy and provide guidance regarding design, characterization and validation for equipment and in collaboration with other departments. + Assure agreed validation strategy is properly documented and aligned with procedural and regulatory requirements by reviewing and approving validation documentation. + Provide support to Plant QA regarding equipment or information system related production issues.
Requirements+ Master degree related to the pharmaceutical industry + More than 5 years of experience in a GMP environment + Relevant experience with equipment and automation validation + Fluent in English
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Suleyman Ekiz.