QA Supervisor

Roles & Responsibilities
• Manage Change Control, Deviation, CAPA, and Complaint modules
• Review and monitor equipment and utility re-qualification programs
• Periodic review of Process Validation Programs and VMP deliverables
• Conduct and coordinate internal, third-party, and regulatory audits
• Plan, conduct, and coordinate GMP and quality training programs
• Manage and review third-party quality systems and compliance
• Prepare, review, and approve SOPs, BMRs, and BPRs
• Review, control, and maintain all technical and quality documentation
• Provide validation support for new plant projects and initiatives
• Support QA management in preparation and response to regulatory audits
• Report GMP and regulatory non-compliances to Head of Quality
• Assist Head of Quality in cGMP implementation and quality problem-solving

Qualification
• Bachelor’s degree in Pharmacy or Science

Experience
• 5–8 years of experience in the pharmaceutical industry

Skills
• Strong knowledge of QMS, cGMP, validation, and regulatory compliance
• Proficient in MS Office, QMS tools, and quality software systems
• Excellent presentation, documentation, and communication skills in English

About the Organization
Globalpharma Co. LLC is a well-established pharmaceutical manufacturer committed to delivering high-quality, compliant healthcare products. The company follows stringent global quality standards and offers professionals a structured environment focused on regulatory excellence and continuous improvement.