INTERNSHIP DETAILS

LEAP Long Term Intern — Raw Materials Laboratory (11 months)

CompanySanofi
LocationLüleburgaz
Work ModeOn Site
PostedApril 14, 2026
Internship Information
Core Responsibilities
The intern will perform quality control analyses of raw materials and products while maintaining accurate documentation in the LIMS system. They will also support stability testing, equipment maintenance, and investigations into out-of-specification or out-of-trend results.
Internship Type
full time
Company Size
157
Visa Sponsorship
No
Language
English
Working Hours
40 hours
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About The Company
Headquartered in Paris, France, it is the fifth largest pharmaceutical company in the world [3] and is dedicated to the research, development, production and marketing of pharmaceutical products in seven main areas: cardiovascular disease, thrombosis, oncology, diabetes, central nervous system, internal medicine and vaccines.
About the Role

Location: Lüleburgaz ,Turkey

Job Type: Intern

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About the Job

Our Team

The Raw Materials Laboratory at Sanofi's Lüleburgaz Plant plays a critical role in ensuring the quality and safety of pharmaceutical products. Our team is responsible for the analysis and quality control of raw materials, finished products, and validation samples — all in line with the highest industry standards. We are a collaborative, detail-oriented team committed to scientific excellence and patient safety.

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Main Responsibilities

• Perform and report quality control analyses of raw materials and products in accordance with established standards; enter results into the LIMS system and ensure timely approval

• Conduct stability analyses of licensed product samples in line with shelf-life specifications

• Analyze customer complaint samples, process validation samples, equipment cleaning validation samples, and bulk holding time study samples

• Support OOS (Out of Specification) and OOT (Out of Trend) investigations and report findings to the senior specialist

• Follow up on required maintenance and service operations for laboratory equipment

• Perform and record daily checks for laboratory equipment

• Maintain proper archiving of all raw data, quality control reports, and validation documentation

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About You

Education: Currently enrolled in the 3rd year of an undergraduate program or the 1st year of a graduate program in Chemistry or Chemical Engineering

Technical Skills:

• Familiarity with HPLC and dissolution equipment

• Knowledge of chromatographic analysis and Data Integrity principles

• Proficiency in MS Office programs

• Knowledge of recording, documentation, and reporting practices

Soft Skills: Responsible, team-oriented, result-focused, with strong communication skills

Languages:  Fluent in English (written and spoken)

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Pursue Progress, Discover Extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

#LI-EUR

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

Key Skills
Quality controlHPLCDissolution equipmentChromatographic analysisData integrityLIMSStability analysisDocumentationReportingMS OfficeLaboratory equipment maintenanceChemical analysisValidationOOS investigationOOT investigation
Categories
Science & ResearchHealthcareManufacturingEngineering