M.Pharm

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.

Responsible for monitoring of cGMP activities at site and to have the oversight, monitoring and compliance with quality system.

Monitor and route incoming safety information to the appropriate project teams. Record all ICSR documentation and track cases in accordance with sponsor/customer specifications; distribute incoming mail and faxes.

The ideal candidate will have expertise in Pharma Research & Development and proficiency in MS Excel. Experience in PV Case Processing and Pharmacovigilance & Safety Ops is a plus. The role involves a hybrid work model with rotational shifts.

Formulation Analytical Method development using HPLC/GC/IC/Potentiometry, Brazil-Regulatory analytical experience is mandatory

The CTC supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable.The role is critical to meet planned Site Ready dates

Responsible for ensuring operating state of cGMP compliance in Solution/Emulsion preparation, vial/ampoule washing, Depyrogenation, Filling, Capping and Collection operations.

Master / Integrated Masters in Organic / Pharmaceutical / General Chemistry with experience in organic synthesis. CSIR-National Chemical Laboratory, Pune

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