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7 дней назад

Senior Scientist QC (GMP)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Switzerland
Релокация
Switzerland
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Senior Scientist QC (GMP): Strengthening GMP compliance and quality improvement across Quality Control organizations with an accent on laboratory processes, data integrity, regulatory requirements, and inspection readiness. Focus on leading deviation investigations, identifying root causes, developing CAPAs, and coordinating cross-functional improvement projects.

Location: Visp, Switzerland; onsite. Relocation assistance is available for eligible candidates and their families.

Company

hirify.global manufactures medicines and supports the development of life science therapies.

What you will do

  • Assess QC processes against GMP requirements, identify compliance risks, and implement lasting improvements.
  • Translate regulatory requirements into practical guidance on laboratory processes, data integrity, and documentation.
  • Support inspection readiness and regulatory inspections, advising QC teams on compliance questions.
  • Lead deviation investigations, identify root causes, and develop corrective and preventive actions.
  • Review and approve compliance documentation and quality records.
  • Lead cross-functional improvement projects with QC, Quality Assurance, Manufacturing, and Technical Operations, using quality metrics and trends.

Requirements

  • Master’s or doctoral degree in life sciences, chemistry, pharmacy, biotechnology, or a related field; alternatively, a bachelor’s degree with extensive relevant experience.
  • At least two to three years of experience in a GMP-regulated pharmaceutical or biotechnology environment.
  • Practical knowledge of Swissmedic, FDA, and EU GMP requirements, EMA expectations, ICH guidelines, and the US and European Pharmacopoeias.
  • Experience working with regulatory authorities, supporting inspections, and leading deviation investigations and CAPAs.
  • Experience identifying compliance gaps, applying quality risk management, and leading cross-functional improvement projects.
  • Clear communication skills in English are required. Strong technical writing, analytical, communication, and collaboration skills are expected.

Nice to have

  • German language skills.

Culture & Benefits

  • Opportunities for career development and leadership of meaningful quality improvements.
  • Inclusive and ethical workplace where employee ideas are valued.
  • Competitive salary and performance-oriented compensation programs.
  • Lifestyle, family, and leisure benefits.
  • Collaborative environment guided by accountability, excellence, passion, and integrity.

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