Project Manager - Cell Production
DEPARTMENT / DIVISION
Executive Management / Project Management
Reporting to the Project Director, you will be responsible for the pharmaceutical development of products at the clinical studies stage and the clinical production of these products, in keeping with good manufacturing practises for medications (GMP production, clinical research and certification). You will implement cell and tissue culture and production units.
You will coordinate and take part in the efforts associated with the preparation of various documents: production, control, documents required for regulatory submissions, financial analyses and feasibility studies. You will identify the critical milestones and possible bottlenecks in the development and implementation of production units, provide progress reports and consolidate contingency plans.
As the project manager, you will work closely with the R&D, business development, regulatory compliance, and legal departments as well as with business partners.
You have a university degree in science (pharmaceuticals, chemistry, biology or biochemistry) combined with academic training in administration. You have at least five years of pertinent experience in product development in the pharmaceutical, blood, tissue, organs and stem cell industry. You are creative and skilled at dealing with uncertainty in a changing and innovative context. You have excellent skills for developing interpersonal relations and are autonomous, flexible and focused on results. You master both official languages, both written and oral. Although this position is based at the Montréal facility, you must be available to travel Québec on a frequent basis.
Héma-Québec is committed to the equal access employment program and invites women, Aboriginal people, members of visible and ethnic minorities and persons with disabilities to apply.