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 an R&D Senior Analyst

The R&D Senior Analyst resides to the Product Development Department and her/his main responsibilities involve in brief, but not limited to the following:

         Responsibilities

• Execution of analytical method development.
• Execution of analytical method validation/verification.
• Drafting of analytical method validation protocol and report.
• Monitoring of the equipment and instruments of the R&D laboratory in order to minimize down time and lower maintenance costs.
• Providing technical support including but not limited to analytical method validation/verification protocol and report drafting, evaluation of the analytical results provided by the laboratory.
• Troubleshooting of equipment and instruments of the laboratory.
• Communicating with providers of equipment required in the R&D laboratory.
• Training, development and performance retention of the members of the R&D laboratory

         Requirements

• Bachelor’s degree in Sciences, preferably in Chemistry.
• Professional experience of at least four (4) years in the field of pharmaceutical analysis.
• Experience in analytical method development, validation and verification.
• Fluency in English both written and oral
• Excellent computer literacy (MicroSoft Office)
• Be multitasking
• Cope with deadlines
• Candidates should be up-to-date with the EU guidelines on pharmaceutical development requirements.

   

  Benefits

• friendly and challenging environment
• Competitive salary
• Private insurance
• Personal development opportunities