Associate Technology Transfer Project Manager

Thermo Fisher Scientific Ferentino, Lazio

About the Job

Associate Technology Transfer Project Manager

When you’re part of Thermo Fisher Scientific, you’ll do challenging work, and be part of a team that values performance, quality and innovation. As part of a successful, growing global organization you will be encouraged to perform at your best. With revenues of more than $24 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world.

Location/Division Specific Information

The pharmaceutical manufacturing plant in Ferentino (80km from Rome), with more than 850 employees, is specialized in commercial contract manufacturing of injectable drugs, both liquid and lyophilized formulations, with an increasing focus on biologics.

How will you make an impact?

You will be part of a dynamic and result-driven environment and, as an Associate Technology Transfer Project Manager, you will be instrumental in ensuring clients satisfaction and business growth. The Associate Technology Transfer Project Manager is part of the Business Management Department and coordinates and manages the technology transfer process and scale up of new pharmaceutical products introduced in our commercial manufacturing departments.

What will you do?

  • Support and may coordinate the control of the project progress including maintaining continuous contact with the clients, identification and troubleshooting of the technical problems supported by the specialists, and by providing production and QC assistance in the project introduction initial phases, i.e., analytical transfer, installation feasibility studies, trials, batch validation
  • Generate key documentation including the, Technology Transfer Master Plan/Scope, Process Gap Analysis between receiving site and transferring site, Technology Transfer Report, Project Timeline and Action Item lists
  • Oversee planning, execution and closure of all Engineering/Feasibility/Development phase activities.
  • Hold regular meetings and correspondence between internal and client teams
  • Provide support as needed to Validation and Production during the Validation/Stability phase, including review and approval of process validation documents.

How will you get here?

  • Scientific/pharmaceutical degree (FCT, Pharmacy, Chemistry, Biotecnology)
  • Experience in Pharma industry, preferably in Sterile Manufacturing.
  • Experience on writing or reviewing of Risk Assessments /FMEA/HACCP documents in support to the Process validation.
  • Experience as a Validation Specialist is an added value
  • Familiar with Process Validation general principles and practices

reported in the Guidance of Industry.

Knowledge, Skills, Abilities

  • Capacity to manage the technical relations with the clients
  • Negotiation skills
  • Communication skills
  • Commercial orientation
  • Ability to manage the projects
  • Attention to costs and timings
  • Fluent in Italian and English

At Thermo Fisher Scientific, each one of our 70,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner and safer