Quality Assurance Professional

About the role

We are looking for a Quality Assurance Professional to support our global pharmaceutical operations. The role involves ensuring that all quality documentation, processes and inspections meet regulatory and internal standards.

Key responsibilities

• Prepare, review, issue, distribute and archive quality documents such as SOPs, forms, specifications and work instructions.
• Maintain document‑control systems and guarantee that only current, approved documents are in use.
• Support review of Batch Manufacturing Records, Batch Packaging Records and related compliance documentation.
• Assist in QMS administration, including deviations, CAPAs, change controls, customer complaints and non‑conformance records.
• Track quality events, conduct routine GMP inspections of manufacturing, packaging, warehouse and laboratory areas, and report findings to the QA Supervisor.
• Coordinate GMP and quality‑related training records, monitor employee training compliance and aid onboarding of new staff.
• Support internal, supplier and regulatory audits, prepare audit documentation and follow corrective‑action plans.
• Assist with equipment qualification, process, cleaning and computerized system validation documentation and maintain validation files.
• Participate in continuous‑improvement projects and collaborate with Manufacturing, QC, Warehouse, Procurement and Operations teams.

Required profile

• Bachelor’s degree in Pharmacy, Chemistry, Biology, Chemical Engineering, Biochemistry or a related field.
• Preferably 2 + years of experience in a quality‑assurance environment.
• Excellent written and verbal communication skills.
• Fluent in English.

Required skills

• Good knowledge of GMP principles.
• Experience with QMS processes (deviations, CAPA, change control).
• Familiarity with audit procedures and validation documentation.

What we offer

• Opportunities for personal and professional growth in a dynamic, open environment.
• Commitment to diversity and an inclusive workplace.
• Access to global resources and cross‑functional collaboration.