About the Role
Support quality systems and documentation to help ensure products and processes meet applicable standards and internal requirements.
Key Responsibilities
- Review batch records, standard operating procedures and quality documents.
- Support deviations, change controls, CAPA and internal quality reviews.
- Coordinate with production and quality-control teams for timely compliance.
- Maintain accurate records and assist during audits.
What We Are Looking For
- B.Pharm, M.Pharm or an equivalent relevant qualification.
- Working knowledge of GMP documentation and pharmaceutical quality systems.
- Strong attention to detail and clear written communication.
- Relevant pharmaceutical quality-assurance experience is preferred.
Equal Opportunity
Iatric Pharmaceuticals considers applicants based on skills, experience and suitability for the role. Please submit accurate information and your latest resume.