7 дней назад
Senior Scientist QC (GMP)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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.
Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →
Похожие вакансии
7 дней назад
Quality Assurance Manager (Pharmaceutical)
105 000 - 135 000$
7 дней назад
Senior Specialist External Quality (Pharmaceutical Quality)
6 дней назад
Sr Mgr Product Quality Integrator (Biotherapeutics)
7 дней назад
Microbiologist III - 2nd Shift (Pharmaceutical Microbiology)
44 - 48$
6 дней назад
EMEA Senior Director Medical Affairs (MedTech)
5 дней назад
Associate Director Radiopharmaceutical Clinical Applications – East Central (AL, AR, IN, KY, MS, NC, TN, VA, WV) (Radiopharmaceuticals)
163 000 - 245 000$