At Getz Pharma, our mission is to make a global impact by developing and delivering safe, effective, and high-quality medicines that improve the lives of men, women, and children. Be part of a company where your work directly contributes to better health outcomes and a healthier world.

Why Join Getz Pharma as a Quality Assurance Manager?

Be a Key Leader in Quality Excellence

• Lead and mentor a team ensuring compliance with local and international standards (ISO, GMP, FDA), while managing validation, audits, and quality data across multiple sites.
• Work with QA leadership to design, implement, and improve the company’s Quality Management System (QMS).
• Supervise across different sites, provide coaching, conduct performance evaluations, and lead training programs on GMP, GDPMDD, ISO 9001, and RQA standards.

Drive Compliance and Continuous Improvement

• Spearhead quality initiatives and process improvements that directly impact product safety, compliance, and customer satisfaction.
• Handle deviation and change management procedures, lead Environmental Management System (EMS) programs, and spearhead quality improvement initiatives through cross-functional coordination.

Lead Internal and External Audits

• Act as internal auditor and lead audits with clients, third-party service providers, and government agencies (FDA/PDEA). Manage CAPAs, follow up on non-conformities, and ensure timely and effective corrective actions.
• Work closely with cross-functional teams, clients, and regulatory bodies, gaining exposure and leadership in both internal and external audits.

Be a Driving Force Behind Safe and Trusted Healthcare

• Take a leading role in ensuring the integrity, safety, and quality of pharmaceutical distribution and manufacturing that directly impacts the lives of millions across the Philippines.

Qualifications

• Bachelor's Degree in Pharmacy, Medicine, Life Sciences, or any other related field.
• 3–5 years of experience in Quality Assurance and Management Systems.
• Strong background in Regulatory Compliance, Risk Management, and Safety Reporting.
• Familiarity with ISO 9001:2015, GMP, GDPMDD, and FDA regulatory inspections.

Please refer to job description.