About the role
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 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 sophisticated analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global organization of more than 100,000 colleagues delivers an outstanding 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, Patheon and PPD.
Monza site is an outstanding pharmaceutical contract manufacturing and development facility, specialized in aseptic injectable drugs, with a growing focus on biologics. Joining more than 1800 colleagues on site, the selected candidate will experience an excellent, international, and fast-growing environment. With revenues exceeding $24 billion and the largest investment in R&D in the industry, we give our people the resources and chances to create meaningful contributions to the world.
Overview: The Technology Transfer Project I will lead and manage the introduction of new pharmaceutical products in commercial manufacturing. TTPM I operates under close supervision, focusing on managing dedicated project streams and ensuring project requirements are documented and risks communicated effectively.
Responsibilities:
* Ensure that client’s project requirements are accurately received and processed by internal functions. * Define and supervise project scope, timing, progress and risks. * Manage Tech Transfer interdisciplinary groups, ensuring effective task assignment and coordination. * Coordinate the start, progress tracking, and completion of projects by staying in regular communication with team members to address and solve issues. * Lead changes and improvements strategy for assigned project, focusing on cost savings and adherence to cGMP and company procedures. * Contribute to team capability development, including materials management.
* Required Skills: * Master’s degree (pharmacy, chemistry, biology, biotechnology or similar). * 0-2 years of experience within a GMP manufacturing facility or related internship experience. * Basic understanding of technical issues and requirements for new product introduction. * Knowledge of aseptic product manufacture is preferred. * Basic planning and organizing skills, including risk management and technical writing skills. * Strong interpersonal skills to build and manage relationships with clients and team members. * Ability to support and assist cross-functional teams. * Good communication skills, both written and oral.