Global GMP Quality System Manager- (Contractor)

Global QMS Governance | GMP Compliance | Continuous Improvement|6-Months
We are seeking an experienced Global Senior GMP Quality Systems Manager for a six-month contractor assignment within an international biopharmaceutical environment. The role will focus on strengthening and continuously improving a global Quality Management System.
Key Responsibilities
Develop, implement and maintain an agile, compliant global GMP Quality Management System.
Lead the harmonisation and continuous improvement of quality processes across manufacturing and supply-chain operations.
Monitor GMP performance indicators, identify trends and drive corrective and preventive improvements.
Support global inspection readiness and provide GMP expertise during audits and regulatory inspections.
Assess new and changing regulations and translate them into effective processes and procedures.
Develop and maintain GMP training programmes.
Support and enhance electronic Quality Management Systems (eQMS).
Collaborate with global Quality, Operations, Regulatory Affairs, Supply Chain, Validation, IT and external manufacturing partners.
Promote a strong quality culture across an international, cross-functional organisation.
Your Profile
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.
This is an opportunity to take on a highly visible global assignment and make a meaningful contribution to regulatory compliance, operational excellence and continuous quality improvement.