What are the responsibilities and job description for the Project Manager - cGMP Compliant Development position at CAMRIS?
CAMRIS International, LLC is a dynamic medical research and development firm that achieves innovative solutions to health and development challenges through high-quality, cost-effective programs and research management services. We combine our proven systems with today's most effective, evidence-based best practices.
We are seeking a talented Project Manager to support the development and manufacturing of pharmaceutical products at our Pilot Bioproduction Facility (PBF). As a Project Manager, you will be responsible for managing development and manufacturing program schedules, assembling performance reports, and delivering high-quality results.
The ideal candidate will have a strong background in project management, including experience with MS Project and resource planning, and a minimum of 12 years of biologics development or manufacturing industry experience. You will lead the PMO team and strategically deploy resources to manage and deliver over 20 successful process development and manufacturing projects.
You will also develop Gantts, including workforce resource assignments for each program, evaluate schedule constraints, risk, and feasibility of performing projects, and direct leadership and interface with PBF clients as required to optimize PBF productivity and quality of services.
