Jodas is a Global, specialty, innovation driven, emerging, generic bio- pharmaceutical company, that is asserting itself among the worlds foremost pharmaceutical companies.
AstraZeneca contributes meaningfully to the UK beyond the provision of our medicines and the benefits they provide to the health of the nation. We commissioned a report in 2009 to measure our significant investment to the UK economy, which includes investment in jobs and wealth creation. Oxera, an independent economic consultancy provided the analysis for this report.
Post : International Associate Regulatory Affairs Director I
Candidate must have hands on experience in Sterile, Parenteral, Aseptic, Filling, Sealing, Filtration, Production QMS, Batch Manufacturing, Autoclave, Terminal Sterilization, Packing Line
Awareness of global pharmaceutical legislation specifically linked to regulatory CMC aspects in the ICH countries. Excellent written and spoken communication skills in English
Method transfer of Pharmaceuticals Products and Materials. Analysis of In-process, Finished products and Stability study samples.
Sampling and testing of Raw Materials, Packaging Materials and Water samples.
You will be responsible for executing or assigning the execution of batch records and log books, filling in various applicable formats, including line clearance and sampling formats, along with batch records review sheets.
Candidate should be proficient in GLP. HPLC. GC. Instrumentation, Chemical Analysis, Raw Material Analysis, FG Analysis, UV, FTIR, In-Process Sample Analysis, and Stability Sample Analysis.
Good analytical hand, well experienced in wet chemical analysis. Hands on experience of GC, HPLC, UV preferred. Aware of Good Manufacturing and Good Laboratory practices. Well versed with documentations related to a pharma laboratory.