Bachelor’s degree or foreign equivalent in Industrial Management, Biotechnology, Pharmaceutical Science, or a related field and 10 years of experience in pharmaceutical development.
Must have at least ten (10) years of experience with: supervising teams of 8+ pharmaceutical professionals and leading Project Management Teams; launching new products in a commercial setting; Manufacturing and Production, technology transfer, and cGMPs, FDA, EU, and ICH guidelines; reviewing and approving Chemistry, Manufacturing & Controls (CMC) content of regulatory submissions; participating in pre-approval inspections by FDA and other regulatory agencies; all phases of chemical and pharmaceutical production operations and lifecycle, including production scheduling, production equipment and validation, and determination of relevant technologies and product types; chemical and pharmaceutical cross-functional operations such as Supply Chain and Engineering, product and tech transfer; business, scientific and personal computer hardware and software applications, including MS Office, including Word, PowerPoint, Excel and SharePoint; and managing diverse project activities with pharmaceutical drug product manufacturing facilities at different geographical locations.
Travel < 5% to meet with colleagues at other affiliated facilities nationally and/or internationally.
This opening is eligible for Actavis Laboratories FL, Inc’s Employee Referral Program incentives.
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