Incyte Internship 2026 in Switzerland | Apply Now For GMP Quality Assurance Role
Gain practical experience in the quality systems supporting commercial pharmaceutical manufacturing. This Incyte Internship offers current MSc students a six-month opportunity to contribute to quality documentation, supplier oversight and compliance activities within the Commercial Manufacturing QA team in Morges.
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Position: GMP Quality Assurance, Intern
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Location: Morges, Switzerland
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Team: Commercial Manufacturing Quality Assurance
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Job ID: 6839
About The Company
Incyte is a global biopharmaceutical company focused on hematology and oncology, alongside inflammation and autoimmunity.
The company is an equal opportunity employer and recruits only through its official careers website. It never asks applicants for money.
Incyte Internship: Role Overview
The Commercial Manufacturing QA team oversees the quality of commercial manufacturing for drug substances, drug products, and primary and secondary packaged products.
The intern will support the maintenance and compliance of Incyte’s Quality Management System, collaborating with colleagues across manufacturing QA, Supply Chain, Commercial Operations and Regulatory Affairs.
Key Responsibilities
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Coordinate the collection of contract manufacturing organisations’ Annual Product Quality Review (APQR) reports and support preparation of Incyte APQR reports.
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Support vendor management through Veeva Organizations updates and vendor statements.
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Review and harmonise QA document classifications in the electronic document management system.
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Help collect small-molecule vendor batch documentation for Incyte batch disposition.
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Support the management and monitoring of Supplier Change Notifications, internal and external CAPAs, and product complaints.
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Assist with implementing and monitoring internal quality KPIs.
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Follow company policies, regulatory requirements and safety procedures.
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Contribute to a culture of business integrity and ethical conduct.
Qualifications and Availability
For this Incyte Internship, applicants must be currently pursuing an MSc in Chemistry, Biology, Pharmacy or an equivalent discipline and be available for a six-month internship at 80–100% workload.
The role also requires:
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Good organisational and communication skills.
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Diplomacy, commitment and effective collaboration.
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Ability to write technical documents.
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Fluent written English and B2-level spoken English, the company’s working language.
French language skills are an advantage.
Cross-Functional Experience
The internship involves cooperation with:
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Supply Chain.
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Commercial Operations.
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Regulatory Affairs.
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Small Molecule Clinical Manufacturing QA.
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Biologics Manufacturing QA.
This provides exposure to how quality documentation, supplier information and compliance activities connect across pharmaceutical operations.
For MSc students interested in pharmaceutical quality assurance, this Incyte Internship offers an opportunity to develop documentation and coordination skills while learning how commercial manufacturing quality systems operate across teams and external partners.
Questions and comments