Quality Assurance Compliance Specialist

Job description:

• Responsible for activities related to writing risk assessments, conducting root cause investigations, and managing CAPA (Corrective and Preventive Actions) processes associated with identified risks.
• The role requires the ability to evaluate manufacturing processes, assess materials, and draw meaningful conclusions. Strong critical thinking, independent work capabilities, analytical skills, and self-learning are essential. The position also involves cross-functional interaction with various departments within and outside the organization.

Basic Requirements:

• Master’s degree in Organic Chemistry – an advantage
• Preference for candidates with 3+ years of experience in the pharmaceutical industry
• Advantage for candidates with project and/or team management experience
• In-depth knowledge of pharmaceutical quality systems, especially those related to risk assessments, investigations, and CAPA processes
• Strong communication skills, excellent verbal and written expression, and full proficiency in English