Ferentino, Frosinone, Italy
23 hours ago
Technical Transfer Engineering Specialist

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

DESCRIPTION:

Join us as a Technical Transfer Engineer at Thermo Fisher Scientific, where you'll contribute to the implementation and optimization of production lines for the transfer of production processes requested by the client and the management of projects that include revamping existing plants or purchasing new ones, liaising with specialized consulting firms, adhering to budgets, GMPs, quality standards, company SOPs, and client confidentiality requirements.

SPECIFIC TASKS/PRIMARY ACTIVITIES

Contribute to the optimal transfer of the production processes requested by the client to the on-site production facilities and their optimization. This is achieved through analysis of the technical specifications transferred by the Technology Transfer team, the possible definition of processes based on the technical specifications, the study of the client's production process, comparison with company processes, gap analysis between the current situation and the desired situation, and the proposal of changes needed for implementation of the new production processes.

Ensure the correct technical and timely assessments needed to prepare Capital Appropriation Requests for financing the assigned projects, respecting the priorities and needs of the requesting Departments.

Ensure the definition of the basic project, the development of design and technical specifications, URS, in line with the needs of the Management and company quality standards.

Support the Purchasing Office in conducting financial negotiations relating to project supplies, adhering to the budget and assigned timelines.

Ensure that activities are managed in line with project technical specifications, quality standards, company procedures and SOPs, and safety regulations.
Contribute to the preparation of appropriate reporting regarding the progress of industrial engineering projects in terms of time, costs, and order status.

This role offers excellent opportunities for professional growth within an established leader in serving science.

REQUIREMENTS:

Bachelor's Degree required, no prior experience required

Preferred Fields of Study: Chemical/Mechanical Engineering, Biomedical Engineering or related scientific field0–2 years of experience in pharmaceutical manufacturing, engineering, or technical functions within a GMP-regulated environment, preferably sterile.Experience in sterile pharmaceutical manufacturingStrong knowledge of GMP, validation principles including IQ/OQ/PQ protocols and FDA/EMA regulatory requirementsExperience with Sterile environmental, equipment design, revamping of existing onesExpertise in Microsoft Office suiteExcellent written and verbal communication skills in EnglishAbility to work independently and as part of cross-functional teamsStrong problem-solving abilities and analytical mindsetExperience with risk assessment methodologiesKnowledge of data integrity requirements and 21 CFR Part 11 complianceAbility to manage multiple priorities effectivelyTravel between sites may be requiredFlexible schedule may be necessary for time-sensitive validation activities

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