Greece Job Openings
Kleva Pharmaceuticals
R&D Senior Analyst
Acharnes
FULL TIME
November 19, 2024
Τοποθεσία Αχαρνές πριν 11 μέρες Ημ. ανάρτησης πριν 11 μέρες Με κάποια εμπειρία Επίπεδο εμπειρίας Με κάποια εμπειρία Πλήρης απασχόληση Τύπος απασχόλησης Πλήρης απασχόληση Φαρμακευτικά / Υγεία Κατηγορία θέσης Φαρμακευτικά / Υγεία
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 (Micro Soft 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
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 (Micro Soft 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
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