Delorbis Pharmaceuticals Ltd invites applications for the position of Quality Batch Documentation Officer based at our premises in Nicosia, CYPRUS.

Main Responsibilities

• Coordinates with Production Department and the Quality Control Department.

• Reviews batch documentation in line with internal batch release procedures.

• Review Production Departments' master documentation.

• Participates in the deviation procedures.

• Maintains the QBD databases.

• Handles and completes the documentation for the supply chain products.

• Manages the Certificate of Analysis (COA) and the Certificate of Compliance/Conformance (COC) templates; prepares and issues the COAs and COCs at the time of batch release.

• Contributes to organize and to evaluate the batch release process.

Experience and Skills:

• A university degree in Pharmacy, Chemistry, Biology, or another relevant scientific degree.

• Able to meet strict deadlines.

• Excellent organizational skills.

• A good command of English, both oral and written; a good knowledge of Greek is an advantage.

• Computer literate with a good knowledge of the most common Microsoft applications

• Previous working experience in the pharmaceutical industry will also be regarded as an advantage.

Please mention the relevant code: QBD-004 for this position and send us your CV by 27th of July 2024 at: hr@delorbispharma.eu

All applications will be treated as strictly confidential.

DELORBIS PHARMACEUTICALS LTD

17 Athinon Street, Ergates Industrial Area

2643 Ergates, P.O. Box 28629,

2081 Lefkosia, Cyprus. Europe.

www.delorbispharma.eu