Founded in 1969, Pharmathen has grown into a leading developer and manufacturer of specialized pharmaceutical products and one of the largest vertically integrated companies in advanced drug delivery technologies. With a strong international presence, we remain committed to improving people’s lives through innovation and access to affordable, high-quality medicines. Today, our products reach patients in more than 90 countries worldwide, supporting better health outcomes every day. Pharmathen employs more than 1,600 people from over 27 different nationalities, reflecting a diverse and international workforce. Our achievements are driven by strong scientific expertise, high ethical standards, and the dedication of our people, who share a commitment to improving patient lives. Pharmathen offers a great opportunity for career development and is seeking to recruit an External Supply Quality Senior Officer to join our Corporate Quality Management team at our Marousi premises. The ideal candidate will be responsible for ensuring compliance with cGMP requirements and ISO standards. More particularly:What you’ll do: Ensure the compliance of the Quality Management System’s Requirements according to cGMPs and International Standard ISO 9001Participate in the company’s Supplier and service provider qualification program. Support the processes for selecting, qualifying, disqualifying and periodically evaluating Suppliers and Service Providers of PHARMATHEN, ensuring compliance with applicable regulations and cGxP requirementsHandle and monitor supplier and service provider’s complaintsHandle and oversee suppliers and service providers' notificationsCompilation, issuance and maintenance of External Supply Quality audit planSchedule of suppliers and service providers audits, support the External Supply Quality Audit Team and participate in suppliers and service providers auditsFollow up external Suppliers CAPA plans and their closuresEscalate External suppliers audit refusals to External Supply Quality upper managementIssuance of Third-party audit report reviewIssue and maintain the List of Qualified External Supply Quality AuditorsMonitor Supplier Quality related KPIsIssue and follow up the Suppliers and Service Providers Quality and Technical AgreementsCoordinate, conduct and maintain the risk assessment of excipients used in medicinal products, as per EU Guideline for excipients (2015/C 95/02)Coordinate, conduct and maintain the external supplier risk assessmentParticipate in the main department’s processes including “Change Control”, “Deviation Investigation Reports”, “Corrective Preventive Actions”, “Risk Management”Responsible for development and review of departmental SOPs, TDRs, protocols and any other relevant controlled quality documents related to the assigned dutiesActively participate in Customers’ Audits and Competent Authorities’ InspectionRequirementsMinimum Qualifications: BSc / MSc in Chemical Engineering, Chemistry, Biology, Pharmaceutical Sciences or other relevant sectorsMinimum Experience:3-5 years of experience in Quality Management / Assurance within the pharmaceutical industry will be considered an assetJob-Specific Skills:Excellent communication in English language (writing & speaking)Computer literacyAbility to prioritize tasks and meet deadlinesExceptional communication skillsStrong project management skillsAutonomous, rigorous with critical thinkingBenefitsWhat you will gain:Involvement in a high-caliber, team-oriented and dynamic atmosphereExposure to challenging business issues and practicesGreat opportunity to leverage and develop your business/ scientific knowledge and skills Join our team and experience the unique Pharmathen’s culture that gives you the opportunity to innovate, to make decisions, to achieve your own potential and to chart your own career.Pharmathen is an equal opportunity employer. We welcome applications regardless of gender, race, age, religion, sexual orientation, and national origin.
Founded in 1969, Pharmathen has grown into a leading developer and manufacturer of specialized pharmaceutical products and one of the largest vertically integrated companies in advanced drug delivery technologies. With a strong international presence, we remain committed to improving people’s lives through innovation and access to affordable, high-quality medicines. Today, our products reach patients in more than 90 countries worldwide, supporting better health outcomes every day.
Pharmathen employs more than 1,600 people from over 27 different nationalities, reflecting a diverse and international workforce. Our achievements are driven by strong scientific expertise, high ethical standards, and the dedication of our people, who share a commitment to improving patient lives.
Pharmathen offers a great opportunity for career development and is seeking to recruit an External Supply Quality Senior Officer to join our Corporate Quality Management team at our Marousi premises.
The ideal candidate will be responsible for ensuring compliance with cGMP requirements and ISO standards.
More particularly:
What you’ll do:
- Ensure the compliance of the Quality Management System’s Requirements according to cGMPs and International Standard ISO 9001
- Participate in the company’s Supplier and service provider qualification program. Support the processes for selecting, qualifying, disqualifying and periodically evaluating Suppliers and Service Providers of PHARMATHEN, ensuring compliance with applicable regulations and cGxP requirements
- Handle and monitor supplier and service provider’s complaints
- Handle and oversee suppliers and service providers' notifications
- Compilation, issuance and maintenance of External Supply Quality audit plan
- Schedule of suppliers and service providers audits, support the External Supply Quality Audit Team and participate in suppliers and service providers audits
- Follow up external Suppliers CAPA plans and their closures
- Escalate External suppliers audit refusals to External Supply Quality upper management
- Issuance of Third-party audit report review
- Issue and maintain the List of Qualified External Supply Quality Auditors
- Monitor Supplier Quality related KPIs
- Issue and follow up the Suppliers and Service Providers Quality and Technical Agreements
- Coordinate, conduct and maintain the risk assessment of excipients used in medicinal products, as per EU Guideline for excipients (2015/C 95/02)
- Coordinate, conduct and maintain the external supplier risk assessment
- Participate in the main department’s processes including “Change Control”, “Deviation Investigation Reports”, “Corrective Preventive Actions”, “Risk Management”
- Responsible for development and review of departmental SOPs, TDRs, protocols and any other relevant controlled quality documents related to the assigned duties
- Actively participate in Customers’ Audits and Competent Authorities’ Inspection
Requirements
Minimum Qualifications:
- BSc / MSc in Chemical Engineering, Chemistry, Biology, Pharmaceutical Sciences or other relevant sectors
Minimum Experience:
- 3-5 years of experience in Quality Management / Assurance within the pharmaceutical industry will be considered an asset
Job-Specific Skills:
- Excellent communication in English language (writing & speaking)
- Computer literacy
- Ability to prioritize tasks and meet deadlines
- Exceptional communication skills
- Strong project management skills
- Autonomous, rigorous with critical thinking
Benefits
What you will gain:
- Involvement in a high-caliber, team-oriented and dynamic atmosphere
- Exposure to challenging business issues and practices
- Great opportunity to leverage and develop your business/ scientific knowledge and skills
Join our team and experience the unique Pharmathen’s culture that gives you the opportunity to innovate, to make decisions, to achieve your own potential and to chart your own career.
Pharmathen is an equal opportunity employer. We welcome applications regardless of gender, race, age, religion, sexual orientation, and national origin.
