3-4

Candidates having previous exposure in EU dossier authoring, product life cycle management, variation and Health Canada filings are preferable.

B.Pharma / M.Pharma; Executive / Sr. Executive for Regulated market (Canada, Australia, Europe)

B.Pharm, M.Pharm, Pharm.D or BDS.; Working knowledge of literature case processing, drug safety regulations and adverse event reporting

Autoclave, Compounding, Vial Filling & Sealing, Vial Washing, Packing, Component Preparation, Capping Operators, LYO. Having Injectable Experience in Production QMS, Deviation ; OOS, OOT and OOL Investigations, QRM Preparation, BMR and BPR Preparation, Audit and Compliance. 

All granulation equipment, compression machine and Auto Coater. Scada PLC Operated Machine RMG, FBP, bag dumping station, preferably have worked with IGL, should have handled all documents in granulation and compression.

Executed end-to-end project management for new product development from project initiation through to filing of the dossier, liaising with cross functional teams to respond to deficiencies and receipt of approval from the regulatory agency.

Experience in routine Analysis, Analytical Method Development as well as Characterization for different products of Orals, Injectables, Peptides, other dosage form and Active Pharmaceutical Ingredients

Established in 2016, ANNORA Pharma is committed to provide medicines with highest quality, safety and efficacy that meets the needs of the customers with applicable statutory and regulatory requirements.

Coordinate for timely vendor payments. Ensure compliance with procurement policies and procedures. Assist in contract negotiations and maintain vendor relationships.