Global Process Validation Engineer – Decontamination & GMP

SKAN AG

Allschwil

Vor Ort

CHF 110.000 - 140.000

Vollzeit

Vor 3 Tagen
Sei unter den ersten Bewerbenden
Bewerbungsgenerator

Eine komplette Bewerbung in einer Minute — maßgeschneiderter Lebenslauf und Anschreiben, versandbereit.

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Benefits dieser Stelle

Open corporate culture
Freedom for ideas
Short decision paths
Job-oriented training
Open communication policy
5 weeks holidays

Zusammenfassung

SKAN AG in Allschwil, Switzerland seeks a Process Validation Engineer (PVE) for the PVM department. The role involves developing and validating decontamination processes (H2O2 and E-Beam) for pharmaceutical isolators and requires up to 50% international travel to customers.

You work in a diverse team, creating test protocols, reports and training customers. Travel across borders is expected and the position offers a competitive benefits package.

Qualifikationen

  • University degree in life sciences, engineering, or technology.
  • Experience with sterilisation technologies and/or isolator decontamination (H2O2 and/or e-beam) is welcome.
  • Experience in cleanroom qualification in medical device/pharma.
  • Experience in process validation (IQ/OQ/PQ) is an advantage.
  • Very good knowledge of English; other languages a plus.

Aufgaben

  • Develop, validate and implement decontamination processes.
  • Create test protocols and test reports.
  • Enable customer-oriented decontamination processes with maximum safety and efficiency.
  • Process optimisation and requalification; customer-oriented troubleshooting and consulting.
  • Carry out internal and external training for customers.
  • Support cross-functional improvements and updates to SOPs and workflows.

Kenntnisse

English proficiency
Sterilisation technologies
Isolator decontamination
Process validation (IQ/OQ/PQ)

Ausbildung

Bachelor’s or Master’s degree (life sciences / engineering / technology)

Jobbeschreibung

SKAN AG in Allschwil, Switzerland seeks a Process Validation Engineer (PVE) for the PVM department. The role involves developing and validating decontamination processes (H2O2 and E-Beam) for pharmaceutical isolators and requires up to 50% international travel to customers.

You work in a diverse team, creating test protocols, reports and training customers. Travel across borders is expected and the position offers a competitive benefits package.

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