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Thermo Fisher Scientific

Technology Transfer Project Manager

Reposted 20 Days Ago
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In-Office
Mississauga, ON
Senior level
In-Office
Mississauga, ON
Senior level
The Technology Transfer Project Manager manages client-related projects, improves client service, and supports business growth through effective communication and project execution.
The summary above was generated by AI

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Summary:

The Technology Transfer Project Manager (TTPM) is able to fully master technical skills with respect to client and business requirements and identifies solutions aligned with these requirements. Responsible for the effective and efficient management of client-related projects to improve client service in the overall best interest of Thermo Fisher.  Supports projects as it relates to Technical Knowledge, Client Experience and Relationship Management and Growth.  

Responsibilities: 

  • Support the definition of new business opportunities while meeting with the existing/potential clients, together with Business Management, during technical meetings with the scope of acquiring new products or the revision of the progress status/completion of projects.
  • Maintain continuous contact with the clients, focusing on the clients’ requirements and the interests of the company. 
  • Generate documents such as the Transfer Checklist, Gap Analysis encompassing process construction, Technology Transfer Master Plan/Scope, Technology Transfer Report, Project Timeline, and Action Item lists.
  • Identify key collaborators for client requests and lead discussions to provide solutions.
  • Lead, track, follow up and lead project activities to ensure alignment with expectations and agreed-upon timeline.
  • Lead all aspects of planning, execution, and closure of all Engineering/Feasibility/Optimization phase activities.
  • Chair regular meetings and correspondence between internal and client teams.
  • Proactively identify, evaluate, and mitigate risks to project timeline or commercial production.
  • Work closely with the Technical Operations to fully understand scope and requirements for projects triggered by events on existing commercial products.
  • Collaborate with Production during the Pre-Validation/ Validation/Stability phase, including review of process validation documents.
  • Provide support as needed to all company functions throughout the course of the project.
  • Champion a positive and collaborative work environment.
  • Ensure cGMP is applied in work area and follows cGMP in all areas of the business. 

REQUIRED QUALIFICATIONS

Education:  

Bachelor’s degree science, engineering, pharmacy, or business.

Project Management Professional (PMP) certification is an asset

Experience:

Minimum 5 years’ previous experience in Engineering, Productions, Quality, or relevant contract manufacturing environment.

Minimum 3 years project management and/or client service experience.

Equivalency:

Equivalent combinations of education, training, and meaningful work experience may be considered.

Knowledge, Skills, Abilities:

Strong communication (both oral and written).  Strong Project Management skills .  Commercial business orientation and financial knowledge. Strong knowledge and understanding of manufacturing/operational processes.  Excellent knowledge of Good Manufacturing Practices and Food and Drug Administration (FDA) compliance knowledge. Effective leadership skills, and the ability to collaborate and empower cross-functional team members.  Ability to meet timelines and prioritize multiple project results. Well organized with strong attention to detail.  Ability to work both in a team as well as independently. Computer proficiency with Microsoft Office programs. Proficiency with the English Language.

Top Skills

MS Office

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