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 R&D Supervisor (at Polydendri site)

  Position Summary:

The R&D Supervisor is part of the Product Development Department, reporting directly to the R&D Manager. This role is responsible for overseeing the analytical R&D laboratory and ensuring the effective development and evaluation of generic pharmaceutical products.

Main Responsibilities

• Supervise the Analytical R&D Laboratory in the development of generic pharmaceutical products.
• Monitor laboratory equipment and instruments to minimize downtime and reduce maintenance costs.
• Provide technical support, including (but not limited to) drafting and reviewing analytical method validation/verification protocols and reports.
• Evaluate analytical results generated by the laboratory.
• Perform troubleshooting of laboratory equipment and instruments.
• Communicate effectively with clients and internal teams, providing analytical information and data for ongoing projects.
• Draft and organize the daily analytical schedule of the laboratory in collaboration with the R&D Manager.
• Liaise with suppliers and service providers regarding R&D laboratory equipment.
• Oversee the training, development, and performance of R&D laboratory team members.

Candidate Profile & Key Qualifications

Academic Background

• Bachelor’s degree in Life Sciences, preferably in Chemistry

Languages:

• Fluency in English both written and oral

Special Knowledge

• Excellent computer literacy (MS Office)

Qualifications 

• Minimum of four (4) years of professional experience in R&D pharmaceutical analysis.
• Proven experience in analytical method validation and verification.
• Strong multitasking and time-management skills.
• Ability to work effectively under tight deadlines.
• Up-to-date knowledge of EU guidelines on pharmaceutical development requirements.

 Benefits

• Work in a friendly and challenging environment
• Competitive salary
• Private insurance
• Personal development opportunitie