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Perform accurate Book-in and data entry ICSRs into safety databases within defined timelines. Ensure compliance with regulatory guidelines, SOPs, and company quality standards for PV processes.

Prior pharma or CRO industry experience working on global clinical studies and projects or global process and system initiatives. Prior experience with Data Management.

Preparation & review of New and Existing Products artwork. Responsible to maintained artworks track records in excel.

Aurobindo Pharma Limited is an Indian multinational pharmaceutical manufacturing company headquartered in HITEC City, Hyderabad, India

To perform the role & responsibilities defined as per TMS software. Escalation to Superior for major non- conformities timely.

Assist in the preparation of response packages to Health Canada requests in a timely manner to minimize delays in the submission review process. 

BS degree in Pharmacy or Life Sciences or relevant education. Minimum 1 year of relevant experience in regulatory affairs, quality or product development in the pharmaceutical, medical devices or similar FMCG industries.

Identify and execute appropriate workup and purification technique to produce an intermediary / final compound of desired quality

Candidate should be science Graduate having good communication skills.