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About Catalent San Diego:
Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.Title: Director Product Development
About Catalent San Diego: Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. The Catalent San Diego site is a premier pharmaceutical chemistry development and manufacturing organization supporting the pharmaceutical and biotechnology industries. We focus on bringing client drug compounds from discovery to the clinic with services that include analytical development, pre-formulation testing, formulation development, GMP (Good Manufacturing Practices) manufacturing and stability storage and testing for Preclinical through Phase 2 programs. At Catalent San Diego, we recruit and develop exceptional individuals with a passion for science and determination to excel. We offer a technically challenging and stimulating environment and the opportunity to learn from the best. For over 25 years, the San Diego site has prioritized employee engagement, good science, and creating customer loyalty, resulting in the opportunity for both growth and stability for our team members while we make a real impact for the patients we support. Summary: Catalent Pharma Solutions is seeking a dynamic leader to join us as Director, Product Development. The Director, Product Development (PD) is responsible for providing operational, scientific and technical leadership for all product development activities, which includes customer-focused programs and programs based with other Catalent operations. This also includes strategically planning future site capabilities and on-boarding of new development and manufacturing technologies. As a leader, the Director, Product Development will enhance and grow the technical and intellectual capabilities of the site while leading a client-centric team capable of solving diverse problem statements for small molecule and peptide therapeutics. The Director will lead the PD team and work in tandem with Project Management, Analytical Development, Engineering, and Manufacturing teams to assure delivery according to agreements with the clients. You will also offer support to sales (BD) and marketing and emphasize the leadership of development programs with a clear awareness of the site’s Quality & Safety culture. The candidate should have extensive industry and management experience, as well as in-depth knowledge of formulation of preclinical and Phase I/II oral and/or parenteral formulations and supporting analytical techniques (such as HPLC and physical characterization). Understanding and application of bioavailability enhancing formulation technologies required. Experience with bioavailability enhancing techniques for oral small molecules is important. Current understanding of cGMP regulations is a must. The candidate must be a self-starter, have excellent written and oral communication skills, problem solving and organizational skills. All duties will be performed in compliance with company standard operating procedures (SOPs) and GMP regulations, as appropriate. The Role:OverviewCommunity Health Center (CHC) is hiring!Medical Assistant SupervisorAt the Community Health Center (CHC), we're not just providing healthcarewere transforming lives. Were a vibrant and inclusive organization dedicated to offering top-notch preventive, primary...
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