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Deputy Manager - Quality Assurance Operations

Centrient Pharmaceuticals NetherlandsWorkableTaunsa, Punjab, India
Posted 9 OctFound 22 OctSeen 17 minutes ago

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The Posting

  • The Role is responsible for reviewing the Batch Production Record, Issuance and Reviewing the Product Labels.

Release of finished products, Verification activities of finished goods at the sites.

Key Individual Accountabilities:

  • Handing & tracking of QMS related activities CAPA, Deviations, Customer Complaints. OOS/OOT, Investigations.
  • Ensure timely review of Batch Production record, Review & approval of investigation, verification of CAPAs, review of QC test results, batch disposition quarantine, rejections approval.
  • Release/Rejection of finished products as per approved specifications.
  • Calibration & Maintenance QA oversight.
  • To perform cleaning verification during product change over and dispatch verification of finished as per established procedures.
  • Verification of reprocessing activities in the site.
  • Handling of Sale Returns.
  • Complying to the laid down norms of Safety Health & Enviroment.
  • Any job assigned time to time by superior based upon training on the procedure.

Requirements

Required Competencies:

  • Working with People
  • Relating & New working
  • Adhering to principles & Values
  • Adapting & responding to changes
  • Coping with Pressure & Setbacks
  • Achieving Personal work Goals & Objectives.
  • Have the Exposure of Audits.

Education: M.Sc. in Chemistry/ M.Pharma

Experience: 10 to 15 years. (Candidate should have API Experience)

Reporting: Manager - QA Operations

Facts

Source
Workable
External id
32CF7803AA
Location
Taunsa, India
Remote
Not stated
Employment
Full time
Posted
9 Oct 2026
First seen
22 Oct 2026, 11:19
Last seen
2 Nov 2026, 21:28
Status
Not yet added
Posting id
bf7be31f-c951-5409-987d-f05845302c56