Quality Batch Documentation Officer
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#DP69990 Type: Full time
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