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Sr Project Manager
| Details |
Country: USA
Location: CA Oakland/East Bay
Total applied: 6
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Sr Project Manager
This opening is located in Alameda, CA
Celera has a successful molecular diagnostics business and powerful genomic and proteomic discovery platforms that have identified and validated new drug targets and biomarkers that will advance the practice of Targeted Medicine. Celera develops and sells a growing number of molecular diagnostic products through a profit-sharing strategic alliance with Abbott Laboratories. In addition, the company is developing new molecular diagnostics and pharmacogenomic tests outside of its alliance with Abbott, and is creating additional value through collaborations based on its genomic discoveries, including new druggable targets, new indications for existing drugs, and pharmacogenomic markers for predicting therapy response. Celera is also using its high-throughput proteomics discovery platform to identify and validate novel targets in cancer. Therapeutic antibodies against these targets are being advanced through strategic partnerships.
Primary responsibility for development, implementation, and support of Design Control Requirements for new product development in support of product development objectives of the Division. Directs the work of project teams who are assigned to specific projects, and coordinates our efforts with that of our strategic partners as needed. Leads multifunctional project teams during the feasibility, development, transfer to manufacturing, launch and regulatory submission phases of our Product Development Process. Plans and manages new product development projects. Develops schedules, monitors progress, and manages resources applied to projects. Reports project status to project team and management. Responsible for training company staff in our Product Development and Design Control processes. Requires B.S. degree in science, or business, or equivalent work experience.
Requires five years experience in project management of projects requiring multifunctional teams and complex project planning, and requires two or more years managing multi-functional project teams developing new diagnostic products requiring meeting FDA standards for Design Control. Must have sound knowledge of the new product development process, from proof of feasibility through development and transfer to manufacturing, ending with assembly of regulatory submissions and launch and initial commercialization of the new products. GMP/QSR experience required. Celera is an Equal Opportunity Employer.
Celera is an Equal Opportunity Employer
Submit Your Resume Online Now
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