Quality Assurance Specialist

This role is responsible for supporting and monitoring quality systems related to clinical supply chain operations, including documentation control, process compliance, and continuous improvement activities. The specialist will conduct internal quality reviews, assist in preparing for audits, support corrective and preventive actions (CAPA), and help ensure adherence to relevant standards and regulatory requirements. Day-to-day responsibilities include reviewing standard operating procedures (SOPs), verifying that operational processes meet quality and GMP expectations, coordinating with cross-functional teams to resolve quality issues, and preparing accurate reports and records.
Qualifications
Candidates should possess skills in Quality Assurance and Quality Management, including implementation and maintenance of quality systems and SOPs.
Candidates should possess skills in Quality Control, including inspection, testing, and verification of processes and documentation.
Candidates should possess skills in Quality Auditing, including participation in internal and external audits and support for CAPA activities.
Relevant experience in pharmaceutical, biotechnology, medical devices, or clinical research environments is beneficial.
Strong attention to detail, analytical thinking, and ability to interpret and apply regulatory and quality standards are required.
Effective written and verbal communication skills, and the ability to collaborate with cross-functional, global teams are important.

Work arrangement
No