GMP QA Intern — Drug Substance & Product Oversight

Incyte Corporation; Morges; Vor Ort; CHF 22.000 - 33.000; Teilzeit

Zusammenfassung

Incyte Corporation in Switzerland seeks a Master’s student for a six‑month internship in Commercial Manufacturing QA. You will help oversee quality activities for Drug Substance and Drug Products, support APQR preparation, and assist in vendor management and document control.

You will contribute to the QA system and ensure compliance with company policies, with collaboration across regulatory, manufacturing, and supply chain teams.

Qualifikationen

• Master degree in Chemistry, Biology or Pharmacy or equivalent.
• Partial to full time six month internship (80-100%).
• Good organizational and communication skills, diplomacy, and commitment.
• Ability to write technical documents.
• English fluency in writing and B2 speaking; French is an asset.

Aufgaben

• Coordinate collection of CMOs APQR reports and support issuance of APQR reports.
• Support vendor management activities and collection of vendor statements.
• Review and harmonize classification of QA documents in eDMS.
• Support collection of SM vendor batch documentation for batch disposition.
• Support management and monitoring of Supplier Change Notifications (SCN).
• Support management and monitoring of internal and external CAPAs.
• Support management and monitoring of Product Complaints.
• Support internal KPI implementation and monitoring.
• Perform duties in compliance with policies, regulations and safety requirements.
• Collaborate with Supply Chain, Commercial Operations, Regulatory Affairs, and QA functions.
• Contribute to a culture of business integrity and ethics.

Kenntnisse

Organizational skills

Communication skills

Diplomacy

Technical writing

English writing

Ausbildung

Master’s degree in Chemistry/Biology/Pharmacy

Tools

eDMS

Jobbeschreibung

Incyte Corporation in Switzerland seeks a Master’s student for a six‑month internship in Commercial Manufacturing QA. You will help oversee quality activities for Drug Substance and Drug Products, support APQR preparation, and assist in vendor management and document control.

You will contribute to the QA system and ensure compliance with company policies, with collaboration across regulatory, manufacturing, and supply chain teams.