RAFARM is a leading Greek pharmaceutical company specializing in the development and production of sterile generics and exporting to more than 60 countries worldwide. The company’s growth journey is shaped by strong global strategic partnerships and ambitious development initiatives, marked by significant milestones — including recent investments that strengthen the introduction of innovation and the development of high value-added medicines, driving continued progress. In parallel, RAFARM maintains a strong commercial presence in the Greek market, serving as a representative for products from international pharmaceutical companies and ensuring patients’ access to high-quality treatments. RAFARM is driven by a team of more than 750 people who cultivate an inclusive environment that enables collaboration, performance, and continuous advancement.
About the role
We are looking for a motivated and detail-oriented Qualified Person to support our Quality Assurance team.
The role main accountabilities will be the following:
- Be responsible for the certification of batches for release in accordance with GMP and company procedures.
- Oversee the quality assurance processes and ensure compliance with regulatory standards of pharmaceutical manufacturing.
- Review and approve batch records, validation documentation, deviations, complaints and change control processes.
- Responsible for final approval of new materials suppliers
- Responsible for identifying the need for new written procedures or for revising existing ones related to all stages of the drug release process.
- Collaborate closely with cross-functional teams to resolve quality-related issues and prevent recurrence.
- Stay updated with industry trends, regulatory updates, and emerging quality management practices.
Requirements
- University degree in Pharmacy, Chemistry, Chemical Engineering or Biology
- Registered Qualified Person status in accordance with EOF regulations would be considered an asset.
- Minimum 5-6 years of experience in Quality Assurance or Quality Control within the pharmaceutical industry.
- Extensive knowledge of GMP, pharmaceutical regulations, and quality systems.
- Excellent managerial and communication skills; ability to effectively collaborate with internal and external stakeholders.
- Detail-oriented with a commitment to maintaining high-quality standards.
- Proficiency in Greek and English language, both written and spoken.
- Experience with regulatory inspections and maintaining compliance with health authority requirements.
Benefits
- Competitive Compensation
- Private Health Insurance
- Career Development Opportunities
- Work-Life Balance
- Company Transportation
- Innovative Work Environment
- Community Engagement
- Recognition and Rewards
Why Join Us At RAFARM, you'll be part of a passionate team dedicated to making a positive impact on global health. You’ll grow your career in a dynamic and innovative environment where your contributions matter.
How to Apply
If you think that the above position suits you, then we are waiting for your application!! Submit your resume here.
After the collection and evaluation of all CV's, we will contact only those candidates who meet the requirements of the position to be filled in order to set an appointment for an interview. All applications are considered strictly confidential.