Technical Transfer Engineering Specialist
Thermo Fisher Scientific
Technical Transfer Engineering Specialist
Job Description
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob 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 field
- 0–2 years of experience in pharmaceutical manufacturing, engineering, or technical functions within a GMP-regulated environment, preferably sterile.
- Experience in sterile pharmaceutical manufacturing
- Strong knowledge of GMP, validation principles including IQ/OQ/PQ protocols and FDA/EMA regulatory requirements
- Experience with Sterile environmental, equipment design, revamping of existing ones
- Expertise in Microsoft Office suite
- Excellent written and verbal communication skills in English
- Ability to work independently and as part of cross-functional teams
- Strong problem-solving abilities and analytical mindset
- Experience with risk assessment methodologies
- Knowledge of data integrity requirements and 21 CFR Part 11 compliance
- Ability to manage multiple priorities effectively
- Travel between sites may be required
- Flexible schedule may be necessary for time-sensitive validation activities
Locations
- Ferentino, Frosinone, Italy
Salary
75,000 - 130,000 USD / yearly
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- GMP complianceintermediate
- Technical specifications analysisintermediate
- Gap analysisintermediate
- Project managementintermediate
- URS developmentintermediate
- Budget adherenceintermediate
Required Qualifications
- Bachelor's Degree required (experience)
- Preferred: Chemical/Mechanical Engineering, Biomedical Engineering or related (experience)
- 0-2 years experience in GMP pharma manufacturing/engineering (experience)
Responsibilities
- Transfer and optimize production processes
- Analyze technical specifications
- Prepare Capital Appropriation Requests
- Define project specs and URS
- Support purchasing negotiations
- Manage projects per SOPs and safety regs
- Prepare project reporting
Answer 10 quick questions to check your fit for Technical Transfer Engineering Specialist @ Thermo Fisher Scientific.
Related Books and Jobs
Technical Transfer Engineering Specialist
Thermo Fisher Scientific
Technical Transfer Engineering Specialist
Job Description
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob 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 field
- 0–2 years of experience in pharmaceutical manufacturing, engineering, or technical functions within a GMP-regulated environment, preferably sterile.
- Experience in sterile pharmaceutical manufacturing
- Strong knowledge of GMP, validation principles including IQ/OQ/PQ protocols and FDA/EMA regulatory requirements
- Experience with Sterile environmental, equipment design, revamping of existing ones
- Expertise in Microsoft Office suite
- Excellent written and verbal communication skills in English
- Ability to work independently and as part of cross-functional teams
- Strong problem-solving abilities and analytical mindset
- Experience with risk assessment methodologies
- Knowledge of data integrity requirements and 21 CFR Part 11 compliance
- Ability to manage multiple priorities effectively
- Travel between sites may be required
- Flexible schedule may be necessary for time-sensitive validation activities
Locations
- Ferentino, Frosinone, Italy
Salary
75,000 - 130,000 USD / yearly
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- GMP complianceintermediate
- Technical specifications analysisintermediate
- Gap analysisintermediate
- Project managementintermediate
- URS developmentintermediate
- Budget adherenceintermediate
Required Qualifications
- Bachelor's Degree required (experience)
- Preferred: Chemical/Mechanical Engineering, Biomedical Engineering or related (experience)
- 0-2 years experience in GMP pharma manufacturing/engineering (experience)
Responsibilities
- Transfer and optimize production processes
- Analyze technical specifications
- Prepare Capital Appropriation Requests
- Define project specs and URS
- Support purchasing negotiations
- Manage projects per SOPs and safety regs
- Prepare project reporting
Answer 10 quick questions to check your fit for Technical Transfer Engineering Specialist @ Thermo Fisher Scientific.
Related Books and Jobs