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Sr Intern, Quality Control
Thermo Fisher Scientific —Ferentino, Lazio
- Tempo pieno
- Microsoft Office
- Laurea magistrale
- Laurea triennale
6 giorni

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Sr Intern, Quality Control

Thermo Fisher Scientific -
Ferentino, Lazio

Candidati adesso

Dettagli della posizione

Tempo pieno
6 giorni fa

Qualifiche

Biologia
Microsoft Office
Laurea magistrale
Laurea triennale

Descrizione completa della posizione

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

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.

Our internship program offers hands-on experience in a pharmaceutical environment, allowing you to apply your academic knowledge to real-world microbiological and quality challenges. You will be part of a team supporting activities that ensure products meet the highest standards of microbiological quality and patient safety.

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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Sr Intern, Quality Control

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