Validation and Quality background is needed, they need to have both. Sterilization validation would be a plus. Equipment validation is important. Lab equipment qualifications. Must work independently. Might be final approver for documents. Excel knowledge a plus. Reviewing and approving documents a major plus. Must be able to work with others as well. Fully onsite. Bachelor’s Degree/Undergraduate Degree in engineering or technical discipline. Master Degree preferred. Experience in pharmaceutical/biopharmaceutical industry or related industry/manufacturing environment. Ability to work on strict deadlines. Background in life science. Ability to interface with cross-functional teams. Detail oriented. Strong working knowledge of Quality System Regulations. Experience leading CAPA (Corrective and Preventive Action) activities. Ability to handle multiple projects concurrently. Well-developed communication skills, both verbal and written.. Years of Experience: 6 – 9 Years
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