Quality Assurance Engineer - Pharmaceutical Projects

About the role

A Quality Engineer is sought to support leading pharmaceutical projects in a dynamic, highly regulated environment. The role contributes to quality assurance and compliance across the pharmaceutical product lifecycle, ensuring adherence to GMP standards and regulatory requirements while working with cross-functional international teams.

Key responsibilities

• Support and maintain Quality Management System (QMS) processes in line with GMP and regulatory requirements.
• Manage and contribute to deviation investigations, CAPA implementation, change controls and risk assessments.
• Take part in internal and external audits, inspections and supplier qualification activities.
• Review and approve quality documentation such as SOPs, protocols, reports and quality records.
• Ensure compliance with pharmaceutical regulations, company procedures and industry best practices.
• Collaborate with Manufacturing, Engineering, Validation, Regulatory Affairs and other stakeholders on quality initiatives.

Required profile

• Bachelor's or Master's degree in Life Sciences, Pharmacy, Chemistry, Biotechnology, Engineering or a related field.
• At least 5 years of experience in a Quality role within the pharmaceutical, biotechnology or life sciences industry.
• Professional proficiency in English.

Required skills

• Strong knowledge of GMP regulations and quality systems.
• Experience with deviations, CAPA, change control, risk management and audit processes.
• Familiarity with international regulatory requirements and quality standards.