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Quality Manager V

4 months ago

Framingham, United States PSG Global Solutions Careers Full time

Apply now and our proprietary system will quickly have you in front of a live recruiter. The Opportunity Description We're looking for a Quality Manager V, working in Pharmaceuticals and Medical Products industry in 31 New York Avenue, Framingham, Massachusetts, 01701, United States. Participate in project teams involved in site biotech facilities, processes and equipment for the manufacture of Drug Substance and/or Drug Product Vaccines.Review and approve validation related studies for assigned areas. These assigned areas would include validation lifecycle activities such as Validation Planning, Biotech ProcessValidation, Equipment and Facility Qualification and Validation Risk Management.Signatory responsibilities for validation/qualification documents within assigned areas. Our ClientOur client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models. Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations. Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.Experience Required for Your Success5+ years experience in a GMP regulated environment working on validation projects associated with biotech processes and equipment.Working knowledge of cGMPs and regulatory requirements.Experience with validation of biotech manufacturing processes (i.e. viral antigen or formulation production) and knowledge of current FDA regulations and industry guidance related to validation processes.Knowledge of vaccines/biologics products and associated technologies.The ability to work on cross functional project teams.Meet/exceed project timelines/deliverables.Experience with Quality Systems including: SAP, Quality eDoc, LabWare, TrackWise and MS Office.What Do You Think?Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible?