About the Position
Pharma Technical Development Europe Biologics (PTDE) brings innovative therapies from the clinical phase to market launch. Our focus is on developing safe and effective medicines using cutting‑edge technologies in manufacturing, clinical supply, formulation, packaging, and analytics.
The Drug Product Clinical Supply Center (PTDE‑C) in Basel produces and fills sterile dosage forms for clinical studies (Phase I–III) in state‑of‑the‑art facilities.
As an Intern you support the Manufacturing Compounding & Visual Inspection chapter in preparing solutions before filling and in visually inspecting vials and syringes. You also gain exposure to related areas such as filling, end‑to‑end manufacturing support, science & technology, and quality assurance.
Responsibilities
Assist colleagues in solution preparation and visual inspection.
Identify, evaluate, and drive improvements within Operational Excellence (Lean & Six Sigma), cGMP (planned events / changes).
Technically evaluate and implement new equipment.
Support team culture (New Ways of Working).
Create and optimize cGMP documents, e.g., work instructions and operating procedures in the applicable quality system (Veeva).
Ensure quality requirements according to cGMP.
Generate process / throughput / product tracking to enable data‑driven decisions.
Assist with self‑inspections, audits, Gemba walks.
Qualifications
Enrolled at a university or college, or have a degree not older than 12 months, preferably in Life Sciences, Pharmacy, or Engineering.
First experience in technical development / manufacturing and/or control of parenteral drug products.
Experience in the pharmaceutical industry (cGMP) or another regulated environment.
Strong teamwork and excellent communication skills in German and English; proactive in approaching colleagues.
Excellent documentation skills.
Proficient with IT systems (e.g., Google Workspace, Google Sheets, MS Office, Smartsheet, Tableau, Minitab).
Engaged, motivated, and highly willing to work independently.
Additional Information
The internship starts as soon as possible. Duration is 9–12 months.
Required application materials: current enrollment confirmation, motivation letter, and CV.
Non‑EU / EFTA citizens must provide a university confirmation that the internship is a mandatory part of the training. Please mention desired start date and duration in your motivation letter.
Roche is an Equal Opportunity Employer.
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