Quality Lead (Pharma Construction)
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
TL;DR
Quality Lead (Pharma Construction): Overseeing site quality for a major pharmaceutical manufacturing facility with an accent on GMP compliance and quality management systems. Focus on implementing validation master plans, directing daily quality activities, and ensuring regulatory alignment during construction and commissioning.
Location: Onsite in Geel, Belgium (Project located in the Netherlands)
Company
is a global project management and engineering firm specializing in the delivery of complex pharmaceutical and high-tech facilities.
What you will do
- Establish and maintain project quality management systems aligned with pharmaceutical industry standards.
- Ensure all construction activities comply with Good Manufacturing Practice (GMP) requirements and regulatory standards.
- Direct daily quality activities across all construction disciplines and contractors.
- Oversee quality documentation, IQ/OQ protocols, and validation master plans.
- Coordinate internal and external quality audits, regulatory inspections, and client assessments.
- Lead investigation and resolution of quality issues and deviations.
Requirements
- Degree in Engineering, Science, Quality Management, or a related discipline.
- Minimum 8+ years in quality management roles on major construction or engineering projects.
- Proven experience in pharma facility construction quality management.
- Deep understanding of GMP and Belgian/EU pharmaceutical regulations.
- Extensive experience with ISO 9001, quality management systems, and validation processes.
- Fluent English is essential.
Nice to have
- Proficiency in Dutch or French.
- Professional quality qualification.
- Experience with cleanroom construction and controlled environment validation.
Culture & Benefits
- Commitment to inclusion and diversity, fostering a culture of mutual respect and belonging.
- Accessible hiring process with reasonable accommodations for candidates with disabilities.
- Opportunity to work on a state-of-the-art pharmaceutical manufacturing facility.
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