Torrent Pharmaceuticals Walk-in Interview 2024.Torrent Pharmaceuticals Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue.
Role & responsibilities
Perform IPQA activities at shop floor in each and every stage of Semi Solid manufacturing and packing.
IPQA overview for clean room area behaviour activity.
To Performed the AQL for the visual inspection of the product.
Review of batch processing records. (BPCR & BPR).
Review of all documents relating to the Warehouse, manufacturing, Packaging prior to batch release.
Review of documents of respective areas and logbooks for adequacy and completeness.
IPQA of Dispensing, Manufacturing, Packaging and Dispatch activities.
Review and Control of electronic batch record (BPR/BPCR) issuance in Records.
To performed sampling of the incoming material (RM/PM/SPM) In process/ Finished product/Validation sample.
To Prepared CPV as per the schedule.
Responsible for regulatory audits with exposure equivalent to regulatory audit.
Desired Candidate Profile
Candidate should have relevant experience in the pharmaceutical Industry, preferably in Semi Solid Formulations and have regulatory exposure to USFDA/ MHRA/EU/TGA etc.
Should have excellent verbal & written communication skills.
Ability to work in dynamic environment.
Should be assertive, proactive, and self-driven.
Interested candidates can reach out at Aishwaryatomar@torrentpharma.com
Role & responsibilities
Experienced QMS candidate (min. 5-7 Years) required for investigation of OOS/ OOT and Lab incident/Deviation.
Technical sound on HPLC/Non-CDS TECHNIQUE.
Good writing skill.
Interested candidates can reach out at aishwaryatomar@torrentpharma.com
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