↳Bachelor’s degree in Life Sciences, Pharmacy, Regulatory Affairs or a related field.
↳At least five years of experience in the pharmaceutical or biotechnology industry, particularly within GMP quality systems or manufacturing.
↳Strong knowledge of international GMP requirements, including FDA, EMA, ICH and PIC/S standards.
↳Proven experience in quality-system design, implementation, governance and compliance.
↳Experience with eQMS platforms, quality metrics, KPIs and Quality Management Reviews.
↳Strong project-management, problem-solving and root-cause-analysis skills.
↳Excellent communication and facilitation skills, with the ability to influence multicultural teams in a matrix organisation.
↳Proactive, pragmatic and solution-oriented working style.
↳Fluent English.
