Role at a glance
- Job function
-
Manufacturing & Skilled Trades Manufacturing & Production
- Salary
- Not Disclosed
- Location
- Allschwil, Switzerland
- Work arrangement
- On-site
- Employment
- Full-time
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Role Summary
The Operator Secondary prepares, performs, and completes GMP-compliant manufacturing and packaging work, including production of clinical trial samples. The role also involves cleanroom and cold-zone work, documentation, equipment and room cleaning, and coordination with colleagues and supervisors.
What You'll Do
- Prepare, perform, and complete manufacturing and packaging orders, including in-process controls (IPCs).
- Clean equipment and machine parts, as well as production rooms.
- Document completed work in accordance with GMP requirements.
- Follow applicable GMP, hygiene, safety, SOP, and order-instruction requirements when manufacturing and packaging clinical trial samples.
- Communicate progress and difficulties to colleagues and supervisors in a timely and appropriate manner.
- Help identify, communicate, and resolve problems and inefficiencies, and contribute to improvement opportunities.
Generated from the employer's posting. Verify important details before applying.
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Original job description
Content provided by the employer
Original job description
Content provided by the employer
Work Schedule
Rotational shift daysEnvironmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)Job Description
·Effiziente, zeitgerechte und GMP-gerechte Vorbereitung, Durchführung und Abschluss von Herstellungs- und Verpackungsaufträgen inkl. Durchführung von Inprozess-Kontrollen (IPCs)
·Effiziente und GMP-gerechte Durchführung der Reinigung von Ausrüstungs- und Maschinenteilen sowie von den Produktionsräumen
·GMP-gerechtes Dokumentieren der durchgeführten Arbeiten
·Einhaltung der spezifischen Vorschriften bei der Herstellung und Verpackung von klinischen Prüfmustern, insbesondere der GMP-Regeln, Hygiene- und Sicherheitsvorschriften und der jeweils relevanten Standardarbeitsanweisungen (SOPs) und Auftragsinstruktionen
·Sicherstellung der aktiven, zeitnahen und angemessenen Kommunikation von Fortschritten und Schwierigkeiten an den Kollegen und Vorgesetzten
·Aktive Mitarbeit bei der Identifizierung, Kommunikation und Lösung von Problemen und Ineffizienz sowie bei Verbesserungsmöglichkeiten
·Arbeiten in Kühlzonen
About the company
Thermo Fisher Scientific
Large Enterprise
Thermo Fisher Scientific is a global leader in serving science, providing a wide range of analytical instruments, reagents, and software solutions for healthcare, pharmaceuticals, and life sciences research. With a commitment to innovation and quality, the company enables customers to make significant advancements in scientific discovery and healthcare diagnostics. Thermo Fisher operates in more than 50 countries and employs over 80,000 people, fostering a collaborative environment aimed at enhancing global health and safety. Through its broad portfolio of brands and technologies, the company plays a vital role in accelerating life-changing research and improving patient outcomes worldwide.