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2 дня назад

Manufacturing Process Expert – Drug Product 80-100% (f/m/d)

Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
c1
Страна
Switzerland
Релокация
Switzerland
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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TL;DR
Manufacturing Process Expert – Drug Product 80-100% (f/m/d) (Sterile Manufacturing/GMP): Executing and improving drug product manufacturing processes with an accent on batch execution, troubleshooting, GMP documentation, and cross-functional technical support. Focus on investigating critical deviations, driving process changes and CAPAs, and resolving complex production issues on the shopfloor.

Location: Visp, Switzerland. Onsite manufacturing role with flexible working hours. Relocation assistance is available for eligible candidates and their families.

Company

hirify.global is a global life sciences company developing products and services that support healthcare and pharmaceutical manufacturing.

What you will do

  • Execute Drug Product manufacturing activities according to cGMP guidelines, including batch execution, batch-data evaluation, and process troubleshooting.
  • Provide frontline technical and procedural support to manufacturing, engineering, and QA operations.
  • Ensure batches are manufactured safely, on time, and in compliance with batch instructions and quality requirements.
  • Prepare and review electronic batch records and other GMP production documentation.
  • Drive manufacturing-process optimization projects and act as a Subject Matter Expert for other departments.
  • Own process investigations and critical deviations, and manage process changes, CAPAs, effectiveness checks, and related GMP systems.

Requirements

  • Bachelor’s or master’s degree in Pharmaceutical Technology, Chemistry, Pharmacy, or an equivalent scientific field.
  • 3–5 years of experience in sterile manufacturing operations, preferably in compounding, filtration, steam sterilization, or single-use systems.
  • Experience with GMP requirements, quality procedures, SOP execution, and deviation or investigation management.
  • Fluent English required; German is an advantage.
  • Strong communication, collaboration, structured working habits, and a proactive, solution-oriented approach.
  • Prepared to work flexible hours.

Nice to have

  • Experience in QA operations.
  • German language skills.

Culture & Benefits

  • Inclusive and motivated working environment.
  • Modern production line focused on continuous improvement.
  • Agile career development and a dynamic working culture.
  • Ethical workplace with a focus on people and the environment.
  • Performance-based compensation programs and role- and location-dependent benefits.

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