Technology Transfer Project Manager - Jobs in Whitby, ON

Job Description

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $25 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or increasing productivity in their laboratories, we are here to support them.How will you make an impactManagement of technology transfer projects and associated activities of pharmaceutical products with their production specifics from internal (PDS) and from external clients to a Patheon commercial facility. The transfer takes place through a feasibility analysis carried out with the support of the subject matter expert; the coordination of the transfer procedures; the assistance to the effective start up of the production; all in respect of the client requirements, cGMP, Patheon’s interests and the company quality standards.What will you doManagement of projects triggered by events on existing commercial products requiring technology transfer management leadership.Chair regular meetings and correspondence between internal and client teamsLead, track, follow up and monitor project activities to ensure alignment with expectations and agreed-upon timeline.Maintain document/information repositoryWork closely with PDS formulator to follow and understand early stage product development for PDS-to-Commercial product transfersWork closely with Process Engineer to fully understand scope and requirements for projects triggered by events on existing commercial productsHelp support the Generate key documentation with input from SME (including Technology Transfer Checklist, Gap Analysis that includes process design, Technology Transfer Master Plan/Scope, Technology Transfer Report, Project timeline and Action Item lists)Oversees planning and support SME for the execution and closure of all Engineering/Feasibility/Optimization phase activitiesProvide support (where needed) to Validation and Production during the Validation/Stability phase, including review and approval of process validation documentsHow will you get thereEducation/Experience:Bachelor’s Degree in a scientific/pharmaceutical area or in engineering. Master’s Degree or equivalent in one of these areas is preferred3-5 years of previous experience in project management. PMP certification considered an assetKnowledge, Skills, Abilities:Excellent Client service/ Project Management experienceExcellent written and oral communication skillsProficient in the English languageAdvanced Negotiation & Communication skillsCommercial business orientation / financial acumenStrong technical skills in pharmaceutical techniques and pharmaceutical production would be an asset.Strong analytical abilities with detail orientationStrong Ability to work and to guide a team as well as independentlyOur global team of more than 75,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services and Patheon. For more information, please visit www.thermofisher.com