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 Sr. Process Engineer - (Job Number: 0806415)

Details
Country: USA
Location: Florida-Gainesville/Jacksonville/Ocala US-FL-Gainesville/Jacksonville
Total applied: 3
Sr. Process Engineer - (Job Number: 0806415)

US-FL-Gainesville/Jacksonville/Ocala Status: Full Time, Employee Job Category: Biotech/R&D/Science Reference Code: 705676 Sr. Process Engineer - (Job Number: 0806415) DescriptionVISTAKON , a division of Johnson & Johnson Vision Care, is a worldwide company with operations in the United States, Japan, Latin America, Asia-Pacific and Europe/Middle East/Africa regions. Research, innovation and new-product development are the focus of our organization. Since we introduced soft disposable contact lenses in 1988, no other manufacturer has matched the aggressive expansion of our wide-ranging ACUVUE family of products. Our associates around the world are committed to expanding the ACUVUE brand, and fortifying our position as the worldwide leader in vision care. The Sr. Process Engineer designs, performs and manages all phases of process development with an emphasis on sterile and aseptic technologies. Considered a subject matter expert, the Sr. Process Engineer performs background research, including, but not limited to, excipient and ingredient selection and evaluation, small-scale experiments, process scale-up, and evaluation of stability data. The position tests innovative technologies that can be used to develop new products, and manages internal/external projects both independently and within a team environment. The Sr. Process Engineer creates product development timelines, budgets and other project management tools; as well as communicates development activities, findings and recommendations to management. The position will mentor junior scientists/engineers in development of technologies to be used for new products. The Sr. Process Engineer supports the Technology Transfer of sterile products to commercial facilities, and will coordinate or manage capital purchases and validation activities as required. Manage pre-commercial contractors, and supervise the manufacture of clinical and regulatory batches. Generate documentation in support of FDA submissions. Evaluate complex technical issues to introduce new products, equipment or processes. Present data and conclusions using appropriate statistical analysis. Initiate and write technical reports with minimal supervision. Analyze data from various sources; draw conclusions and recommends scientific solutions. A minimum of 5 years of experience with BS degree in Pharmacy, Pharmaceutical Science, Chemistry, Chemical Engineering or equivalent discipline or a minimum of 3 years of experience with Masters degree in Pharmacy, Pharmaceutical Science, Chemistry, Chemical Engineering or equivalent discipline or a minimum of 1 years of experience with PhD in Pharmacy, Pharmaceutical Science, Chemistry, Chemical Engineering or equivalent discipline is required. Experience with sterilization, sterile products/processes or aseptic techniques are required. Experience in device or pharmaceutical development required. Experience in research and development is preferred. Experience working in GXP environments is preferred. Strong communication, interpersonal and organizational skills are required. Generally works out details within broad guidelines and exercises considerable initiative and judgment. Effective in oral and written communications at all levels and cross functionally. Executes tasks to completion within deadlines. Works independently with minimal supervision once assignments or responsibilities are outlined and delegated. Works effectively in a multi-task environment with competing priorities. Displays a strong sense of ownership for work. Motivated self-starter with a "can-do" attitude. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of companies, bid on this position today! Apply Now

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