--- title: Quality Systems & Compliance Specialist at GM Pharma description: Quality Systems & Compliance Specialist Company: GM Pharmaceuticals Location: Tbilisi, Kvemo Ponichala, Georgia Employment Type: Full-time, On-site Working Hours: Monday–Friday, 09:00–18:00 About the --- # Quality Systems & Compliance Specialist **Company:** GM Pharma **Location:** Tbilisi, Georgia **Posted:** 2026-10-20 **Apply by:** 2026-12-04 [Apply / View original posting](https://www.linkedin.com/jobs/view/4478663233) ## Job description Quality Systems & Compliance Specialist Company: GM Pharmaceuticals Location: Tbilisi, Kvemo Ponichala, Georgia Employment Type: Full-time, On-site Working Hours: Monday–Friday, 09:00–18:00 About the Company GM Pharmaceuticals is an international, multinational pharmaceutical corporation with 25 years of experience. Its medicines and food supplements are manufactured at its GMP-certified, high-tech facility in Georgia, as well as at manufacturing facilities in Western Europe, including Germany, Spain, Switzerland, Italy, Sweden, and Portugal. Operating in 8 countries and employing more than 700 highly qualified professionals, GM Pharmaceuticals combines innovation with human potential to improve the lives of over 12 million consumers. What We Offer Stable employment Professional development and career growth opportunities Competitive salary with growth opportunities Health insurance Key Responsibilities Develop and maintain Standard Operating Procedures (SOPs). Participate in planning and implementing quality improvement projects. Contribute to the development and standardization of quality risk analysis methodologies. Organize, manage, and document the transportation of pharmaceutical products within the supply chain. Collect, maintain, and electronically archive transportation-related quality documentation. Prepare and manage quality agreements with transportation companies. Manage the qualification and approval processes for distribution and transportation partners. Monitor and periodically evaluate approved distribution and transportation partners. Coordinate validation and qualification activities and related documentation. Manage validation projects, including planning, scheduling, and coordination. Manage and coordinate change control processes. Ensure timely completion of change-related tasks and evaluate the effectiveness of implemented changes. Review and assess supply chain traceability reports. Requirements University degree in Pharmacy (Master's degree preferred). Previous experience in a GMP-compliant pharmaceutical manufacturing facility or quality management system is preferred. Knowledge of international standards such as EU GMP, EU GDP, WHO, ICH, ISO, and USP is preferred. Knowledge of international and local pharmaceutical manufacturing and distribution regulations, including GMP and GDP. Excellent command of Georgian, Russian, and English. Advanced proficiency in MS Office. Key Competencies Strong sense of responsibility and attention to detail Analytical and logical thinking Excellent verbal and written communication skills Strong documentation and organizational skills Effective time management and prioritization Discipline, punctuality, and results-oriented mindset How to Apply Interested candidates are invited to submit their CV by November 1, 2026 , through the official vacancy application page. GM Pharmaceuticals looks forward to welcoming a new professional to its team! --- 🔔 [Monitor similar jobs on Gurify](https://gurify.com/?utm_source=techgeo&utm_medium=jobboard&utm_campaign=monitor_similar&role=Quality+Systems+%26+Compliance+Specialist) — get alerted when matching roles are posted in Georgia. ```json {"@context":"https://schema.org/","@type":"JobPosting","title":"Quality Systems & Compliance Specialist","description":"

Quality Systems & Compliance Specialist Company: GM Pharmaceuticals Location: Tbilisi, Kvemo Ponichala, Georgia Employment Type: Full-time, On-site Working Hours: Monday–Friday, 09:00–18:00 About the Company GM Pharmaceuticals is an international, multinational pharmaceutical corporation with 25 years of experience. Its medicines and food supplements are manufactured at its GMP-certified, high-tech facility in Georgia, as well as at manufacturing facilities in Western Europe, including Germany, Spain, Switzerland, Italy, Sweden, and Portugal. Operating in 8 countries and employing more than 700 highly qualified professionals, GM Pharmaceuticals combines innovation with human potential to improve the lives of over 12 million consumers. What We Offer Stable employment Professional development and career growth opportunities Competitive salary with growth opportunities Health insurance Key Responsibilities Develop and maintain Standard Operating Procedures (SOPs). Participate in planning and implementing quality improvement projects. Contribute to the development and standardization of quality risk analysis methodologies. Organize, manage, and document the transportation of pharmaceutical products within the supply chain. Collect, maintain, and electronically archive transportation-related quality documentation. Prepare and manage quality agreements with transportation companies. Manage the qualification and approval processes for distribution and transportation partners. Monitor and periodically evaluate approved distribution and transportation partners. Coordinate validation and qualification activities and related documentation. Manage validation projects, including planning, scheduling, and coordination. Manage and coordinate change control processes. Ensure timely completion of change-related tasks and evaluate the effectiveness of implemented changes. Review and assess supply chain traceability reports. Requirements University degree in Pharmacy (Master's degree preferred). Previous experience in a GMP-compliant pharmaceutical manufacturing facility or quality management system is preferred. Knowledge of international standards such as EU GMP, EU GDP, WHO, ICH, ISO, and USP is preferred. Knowledge of international and local pharmaceutical manufacturing and distribution regulations, including GMP and GDP. Excellent command of Georgian, Russian, and English. Advanced proficiency in MS Office. Key Competencies Strong sense of responsibility and attention to detail Analytical and logical thinking Excellent verbal and written communication skills Strong documentation and organizational skills Effective time management and prioritization Discipline, punctuality, and results-oriented mindset How to Apply Interested candidates are invited to submit their CV by November 1, 2026 , through the official vacancy application page. GM Pharmaceuticals looks forward to welcoming a new professional to its team!

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