21 set - Ferentino
Thermo Fisher Scientific
**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office
- When_ _you’re_ _part of the team at_ _Thermo_ _Fisher Scientific,_ _you’ll_ _do important work._ _You’ll_ _have the opportunity to grow and learn in a culture that empowers your development. We have built an inclusive, global environment that values diverse talent and fosters innovation._- Customers throughout the globe rely on our extensive range of products and services—from next-generation instruments to everyday lab essentials to life-saving medicine. If you_ _desire_ _joining_ _a world-class team,_ _Thermo_ _Fisher Scientific can provide you with the opportunity to work in quality assurance and regulatory affairs to produce products that enable our customers to make the world healthier,_ _cleaner_ _and safer._ **Summary of Internship** This internship is designed for students in biology, microbiology, biotechnology, pharmacy or related life sciences who are interested in gaining practical experience in a pharmaceutical microbiology and quality environment. You will gain exposure to how microbiological testing, contamination control, and regulatory requirements are applied in industry, and how these contribute to the release of safe and compliant products.
**- Internship Opportunities - Key Learning Areas** Pharmaceutical Microbiology Fundamentals
- Understand how bioburden, sterility, and endotoxins impact product quality
- Gain exposure to routine microbiological testing performed in pharmaceutical laboratories
- Learn the principles of aseptic techniques and contamination control Environmental Monitoring & Cleanroom Practices
- Get familiar with cleanroom classifications and behaviors
- Support activities related to environmental monitoring (air, surfaces, personnel)
- Understand how EM data is used to ensure control of manufacturing areas Sterility Assurance & Filtration
- Learn the basics of sterile filtration and aseptic processing
- Understand how microbiological risks are controlled during production
- Gain insight into validation concepts related to sterility assurance Microbiology & Quality Documentation (GMP)
- Support the review and organization of documentation related to: - microbiological testing (bioburden, EM, endotoxins, sterility)
- deviations and investigations
- Learn how GMP documentation is structured and maintained Introduction to Regulatory Expectations
- Understand how microbiological data supports regulatory submissions
- Gain basic knowledge of FDA/EMA expectations on microbiological quality
- Contribute to documentation used for regulatory compliance
**- Essential Functions**
- Support routine activities related to microbiological quality and contamination control
- Assist in reviewing data from bioburden, endotoxin and environmental monitoring tests
- Collaborate with Quality Control Microbiology, QA and Production teams
- Contribute to GMP documentation,
including data entry, review and organization
- Support investigations of microbiological deviations (with supervision)
- Participate in maintaining compliance with aseptic practices and cleanroom procedures
- Learn how to interpret microbiological results in a pharmaceutical context
- Perform tasks aligned with your academic background and training level
**- Qualifications**
- Student currently enrolled in a Bachelor’s or Master’s degree in Biology, Microbiology, Biotechnology, Pharmacy or similar
- Basic understanding of: - Microbiology (microorganisms, growth, contamination)
- Laboratory practices (e.g. sterile technique)
- Laboratory experience (university labs, thesis, internships) is preferred
- Interest in working in a pharmaceutical or biotech environment
- Strong attention to detail and willingness to follow procedures
- Good organizational and teamwork skills
- Willingness to learn and grow in a structured, regulated environment
**- Thermo**Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate**on the basis of**race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status,**disability**or any other legally protected status.** **This position is a curricular internship within the**Chloropyll**Program’s 2025. It offers a unique opportunity to gain valuable experience and enhance your skills in a dynamic and innovative environment.** **To apply, please**submit**your CV in English. Join us in shaping the future and advancing your career through this exceptional internship program.
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