QA Assistant Manager

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

Qualification
• Bachelor’s degree in Pharmacy or Science

Experience
• Minimum 5 years of experience in the pharmaceutical industry

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

About the Organization
Globalpharma Co. LLC is a leading pharmaceutical manufacturer committed to global quality standards, regulatory compliance, and continuous improvement. The organization provides a professional environment that supports learning, innovation, and long-term career growth.