KLEVA Pharmaceuticals S.A. is a privately owned pharmaceutical and fully integrated company that has been in operation in Greece for over 50 years. Kleva develops and manufactures generic products and focuses on Pharmaceuticals (Rx & OTC).
Our two manufacturing facilities in the North of Athens, Greece, are equipped with high technology machinery and have the manufacturing potential for a wide range of pharmaceutical forms.
Our mission is to offer a flexible, fully scalable, qualitative, and cost-effective product development in a wide range of dosage forms. We register and export our products to a number of regulated and non-regulated markets around the world.
To realize our ambitious goals, KLEVA needs people who are innovators, believe in the values of respect and cooperation and are ready to commit to a company that wants to penetrate new markets, leverage international business development opportunities, and enter contract manufacturing deals.
How you will support our mission
We are looking for Technology Transfer Project Manager
DUTIES AND RESPONSIBILITIES:
The Technology Transfer Project Manager responsibilities are:
- Project Management & Control
- Project Execution: Ensuring projects meet both regulatory standards and customer specifications.
- Progress Management: Tracking, coordinating, and controlling project timelines and progress.
- Financial Control: Managing and controlling the project budget.
- Documentation: Generating and maintaining essential project documentation (e.g., TT Plan, Gap Analyses, Risk Management, timelines, protocols, and reports).
- Client & Stakeholder Communication
- Client Updates: Communicating regularly with clients on project progress.
- Internal Coordination: Organizing regular meetings between the customer and the internal project team.
- Regulatory & Quality Compliance
- Protocol & Report Generation: Issuing and preparing key quality documents like Stability Protocols, Analytical Method Transfer (AMT) Protocols & Reports.
- Dossier Support: Collecting/preparing documentation for the client's product dossier submission and drafting responses to regulatory authority questions in collaboration with management.
PROFILE / SKILLS:
Academic Background
- Bachelor’s degree in Pharmacy, Chemistry, Biology, Chemical Engineering or other related field.
Languages:
- Fluency in English both written and oral
Special Knowledge
- Excellent computer literacy (MS Office)
Qualifications
- Previous professional experience of at least 1-2 years in Project Management or a related field in the pharmaceutical industry is preferred, but not mandatory.
- Knowledge of GMP regulations and ICH guidelines is an advantage.
- Strong attention to detail, organizational skills and team working skills.
Benefits
- Work in a friendly and challenging environment
- Competitive salary
- Private insurance
- Personal development opportunities