--- title: Quality Systems & Compliance Specialist at GM Pharma description: Location: Tbilisi, Kvemo Ponichala Working Schedule: Monday–Friday, 09:00–18:00 Company: GM Pharmaceuticals GM Pharmaceuticals is an international, multinational pharmaceutical corporation with 25 yea --- # Quality Systems & Compliance Specialist **Company:** GM Pharma **Location:** Georgia **Posted:** 2026-09-08 **Apply by:** 2026-10-23 [Apply / View original posting](https://www.linkedin.com/jobs/view/4462265890) ## Job description Location: Tbilisi, Kvemo Ponichala Working Schedule: Monday–Friday, 09:00–18:00 Company: GM Pharmaceuticals GM Pharmaceuticals is an international, multinational pharmaceutical corporation with 25 years of experience . Our medicines and food supplements are manufactured at our high-tech, GMP-certified manufacturing facility in Georgia, as well as at manufacturing sites across Western Europe, including Germany, Spain, Switzerland, Italy, Sweden, and Portugal . Operating across 8 countries with more than 700 highly qualified professionals , GM Pharmaceuticals is a company where innovation meets human potential to improve the lives of more than 12 million people . We are currently looking for a Quality Systems & Compliance Specialist to join our team in Tbilisi. What We Offer Stable employment in an international pharmaceutical company; Professional and career development opportunities; Competitive and growing compensation; Health insurance. Key Responsibilities Develop and maintain Standard Operating Procedures (SOPs) and other quality-related documentation; Participate in the planning and implementation of quality improvement projects, as required; Contribute to the development and standardization of Quality Risk Management (QRM) methodologies and their application to ongoing processes; Coordinate, manage, and document the transportation of medicinal products throughout the supply chain in accordance with applicable quality requirements; Collect, review, and maintain transportation-related quality documentation; Prepare and coordinate Quality Agreements with transportation service providers; Manage the qualification and approval process for distribution and transportation service providers and analyze qualification results; Conduct ongoing monitoring and periodic quality evaluations of approved distributors and transportation service providers; Coordinate documentation and processes related to validation and qualification activities within the company; Manage validation projects, including defining timelines, coordinating activities, and monitoring implementation; Ensure timely completion of actions resulting from approved changes; Review and evaluate supply chain traceability reports ; Manage and coordinate the Change Control process; Evaluate the effectiveness of implemented changes and ensure appropriate documentation and records are maintained. Qualifications & Expercience University degree in Pharmacy ; a Master's degree is preferred; Experience in a GMP-compliant pharmaceutical manufacturing environment or Quality Management System (QMS) role is preferred; Knowledge of international pharmaceutical standards and guidelines, such as EU GMP, EU GDP, WHO, ICH, ISO, and USP , is an advantage; Knowledge of international and local regulatory requirements related to pharmaceutical manufacturing and distribution, particularly Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP) ; Proficiency in Georgian, English, and Russian ; Advanced proficiency in MS Office . Key Competencies High level of responsibility and accountability; Strong logical and analytical thinking; Strong written and verbal communication skills; Ability to accurately document processes and completed activities; Effective time management and prioritization skills; Strong attention to detail; Discipline and punctuality; Goal-oriented and results-driven approach. 🚀Join GM Pharmaceuticals If you are interested in developing your career in Pharmaceutical Quality Systems and Compliance and working in an international GMP-regulated environment, we invite you to apply and become part of the GM Pharmaceuticals 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":"

Location: Tbilisi, Kvemo Ponichala Working Schedule: Monday–Friday, 09:00–18:00 Company: GM Pharmaceuticals GM Pharmaceuticals is an international, multinational pharmaceutical corporation with 25 years of experience . Our medicines and food supplements are manufactured at our high-tech, GMP-certified manufacturing facility in Georgia, as well as at manufacturing sites across Western Europe, including Germany, Spain, Switzerland, Italy, Sweden, and Portugal . Operating across 8 countries with more than 700 highly qualified professionals , GM Pharmaceuticals is a company where innovation meets human potential to improve the lives of more than 12 million people . We are currently looking for a Quality Systems & Compliance Specialist to join our team in Tbilisi. What We Offer Stable employment in an international pharmaceutical company; Professional and career development opportunities; Competitive and growing compensation; Health insurance. Key Responsibilities Develop and maintain Standard Operating Procedures (SOPs) and other quality-related documentation; Participate in the planning and implementation of quality improvement projects, as required; Contribute to the development and standardization of Quality Risk Management (QRM) methodologies and their application to ongoing processes; Coordinate, manage, and document the transportation of medicinal products throughout the supply chain in accordance with applicable quality requirements; Collect, review, and maintain transportation-related quality documentation; Prepare and coordinate Quality Agreements with transportation service providers; Manage the qualification and approval process for distribution and transportation service providers and analyze qualification results; Conduct ongoing monitoring and periodic quality evaluations of approved distributors and transportation service providers; Coordinate documentation and processes related to validation and qualification activities within the company; Manage validation projects, including defining timelines, coordinating activities, and monitoring implementation; Ensure timely completion of actions resulting from approved changes; Review and evaluate supply chain traceability reports ; Manage and coordinate the Change Control process; Evaluate the effectiveness of implemented changes and ensure appropriate documentation and records are maintained. Qualifications & Expercience University degree in Pharmacy ; a Master's degree is preferred; Experience in a GMP-compliant pharmaceutical manufacturing environment or Quality Management System (QMS) role is preferred; Knowledge of international pharmaceutical standards and guidelines, such as EU GMP, EU GDP, WHO, ICH, ISO, and USP , is an advantage; Knowledge of international and local regulatory requirements related to pharmaceutical manufacturing and distribution, particularly Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP) ; Proficiency in Georgian, English, and Russian ; Advanced proficiency in MS Office . Key Competencies High level of responsibility and accountability; Strong logical and analytical thinking; Strong written and verbal communication skills; Ability to accurately document processes and completed activities; Effective time management and prioritization skills; Strong attention to detail; Discipline and punctuality; Goal-oriented and results-driven approach. 🚀Join GM Pharmaceuticals If you are interested in developing your career in Pharmaceutical Quality Systems and Compliance and working in an international GMP-regulated environment, we invite you to apply and become part of the GM Pharmaceuticals team.

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