Aurore Life Sciences is a pure-play API manufacturer, the company is on a mission to become the most preferred partner for pharmaceuticals. Established in 2017, We are a pure-play Active Pharmaceutical Ingredient (API) company keen on delivering superior products in a regulatory compliant environment.
Date and Time:
- Date: 18th September – 20th September, 2024
- Time: 9.30 AM – 2.30 PM
- Venue: Aurore Pharmaceuticals Pvt. Ltd, Plot No 34, 36, 38, 39, 40, 49, 50 and 51, Phase IV, IDA, Jeedimetla, Quthubullapur mandal Mechal District,Telangana-500055
Regulatory Affairs @ Jeedimetla
- Designation: Executive
- Department: Regulatory Affairs
- Experience: 2-5 yrs
- No. Openings: 03
Job description:
- Compilation of USDMFs as per GDUFA requirements in eCTD format.
- Compilation of Annual reports and Amendments to USFDA
- Preparation of Responses comments received from regulatory authority.
- Coordinating with cross functional teams for collection and interpretation of data required for DMF submissions.
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Date and Time:
- Date: 19th September – 20th September , 2024
- Time: 9.30 AM – 3.00 PM
- Venue: Aurore Life sciences private limited , Survey No 180/2, 180/3, Kazipally village, Jinnaram Mandal, Sangareddy District, Telangana-502319
roduction @ Kazipally
- Department: Production
- Designation: Chemist
- Experience: 1-5 yrs
- No. Openings: 10
Job description:
- xecution of the Batch production records like MBPRs, Cleaning BPRs etc Indent and receipt of raw materials and general items Plan the Batch movement as per schedule and maintain the records as per standard operating procedures. Follow the validations as per protocols (Process /Cleaning) Ensuring the raw materials and intermediates storage and handling as per defined procedure/ Instruction.
QA @ Kazipally
- Designation: chemist
- Department: Quality assurance
- Experience: 2-5 yrs
- No. Openings: 10
Job description:
- Issuance, Receipt and review of BPRs, Cleaning records, Forms, Records. Preparation, review, issue and archival of SOPs. Production activity monitoring and reporting. Verification of Calibration records of weighing balances. Preparation and review for Annual Product Review/Product Quality review. Document issuance, retrieval and archival of MBPR, analytical reports, formats etc
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