Job Summary: Oversees the Manufacturing group, which includes Process Development, Technical Transfer, and Operations. Responsible for the operation of a state of the art Cell Therapy facility. Works closely with the groups’ Associate Directors and Area Management to ensure day-to-day MFG operations are performed within Minaris Advanced Therapies Quality standards. Maintains rigorous quality mindset and advocates strict adherence to compliance practices within the department and the facility. Possesses rigorous scientific skills in the specific science area and a strong working knowledge of the technical and current Good Manufacturing Practice (cGMP) compliance requirements for manufacture of biologics. Specific responsibilities include specifying equipment, identification and development of Standard Operating Procedures (SOPs) and Master Batch Records, commissioning and validation as well as staffing and training of the Manufacturing group to be competent in current Good Manufacturing Practices (cGMP). Interacts with Engineering, Maintenance, Validation, Quality Assurance, Facilities, Quality Control, Materials Management groups, and material/equipment vendors and commercial partners.
Essential Job Functions:
Experience / Education
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Physical Requirements:
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability
This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job-related duties as requested by Management.
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