QA Release Supervisor II / III
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
First Shift
Supervisor II, QA :
The Supervisor II, Quality Assurance is responsible for supervising or overseeing a group of employees or a Quality Assurance system, program, project, etc. Participates in employee relations matters and is responsible for performance management in area of responsibility. May occasionally represent quality in meetings. Specific duties will depend on the assignment and may include review of manufacturing or testing records, preparation or review of failure investigations, sampling / testing / data analysis, auditing, data analysis for stability, etc. (i.e. Documentation review, product investigations, product release, internal and external audit support, materials clearance, etc.). The incumbent is an established and technically competent professional who develops and implements solutions to a variety of quality related objectives. He / she may participate on teams or projects of varying scope and is often called upon by peers for his / her expertise or guidance. Demonstrates consistent application of technical knowledge and expertise, executes assignments of medium complexity, developing solutions for defined problems. The employee is responsible for training other employees.
Primary responsibilities for Supervisor II, QA role :
Additional Responsibilities :
Supervisor III, QA :
Responsible for supervising or overseeing a group of employees or a Quality Assurance system, program, project, etc. Participates in employee relations matters and is responsible for performance management in area of responsibility. May facilitate technical and non-technical training. Responsibilities may also include advanced roles (such as author, reviewer, approver, administrator or coordinator) in all quality systems such as Change Control, Discrepancy Management, Quarantine, Batch Release, SAP, SAP Quality Module, Documentation, and Annual Product Reviews as well as provide Quality input for Validation projects, capital engineering projects, clinical studies, stability studies, etps, and Regulatory submissions. Responsible for representing Quality meetings. The employee may be responsible for training or supervising other employees and is a fully qualified professional who requires minimal supervision.
Primary responsibilities for Supervisor III, QA role :
Knowledge, Skills, Abilities for all levels :
Excellent communication skills (written and verbal) with familiarity of domestic (i.e. Food and Drug Administration) and applicable foreign regulatory agency requirements / guidelines.
Education / Experience requirements :
QA Release Supervisor II : BS / BA degree preferably in a STEM (Science, Technology, Engineering, and Mathematics) discipline with minimum of 5 years relevant experience, or equivalent combination of education and experience.
QA Release Supervisor III : BS / BA degree preferably in STEM (Science, Technology, Engineering, and Mathematics) discipline with a minimum of 6 years relevant experience, or equivalent combination of education and experience.
Qa Supervisor • Clayton, NC, US