Sun Pharma Hiring For Quality Control ( Injectable ) Post


Sun Pharma an international,specialty pharmaceutical company headquartered in India with a global manufacturing network across 25 countries. We manufacture and market a large basket of pharmaceutical formulations as branded generics & generics in India, US and across the world.

Job Title : Quality Control ( Injectable )

Experience : 3 – 8 Years

Location : Vadodara/Baroda

Job Description

Quality Control Documentation (Injectable ) – B.Pharma / M.Pharma / M.Sc with 3 to 4 year of experience in QC Preparing & Review of specification, Analytical test procedure & template / Handling of change control & impact evaluation / Handling of Pharmacopoeia changes ./ Documentation control , issuance , retention & procedure/CAPA Assessment . Injectable Regulatory approved formulation plant.

Quality Control Analyst ( Injectable ) – B.Pharma / M.Pharma / M.Sc with 3 to 8 year of experience in QC having experience in / Anaysis of tablet ,capsules ,injectable. Having experience on analytical activity in reputed pharmaceuticals industries having the approval of MHRA, USFDA. JD as follow.

1. In process samples ,Finished product, stability sample analysis on various instrument like HPLC , UPLC , UV ,Spectrophotometer , Dissolution apparatus , KF etc
2. Analysis of tablet capsules, injectable, nasal spreay product.

. To do analysis , accurately & precisely as per approved test procedures & document the analysis as per GMP/GLP norms
4. Calibration of instruments
5. To support / give inputs in LAB activity.
6. Having knowledge of current FDA Guideline.

Quality Control Reviewer (Injectable) B.Pharma / M.Pharma / M.Sc with 3 to 8 year of experience in QC injectable facility having experience in

  • Review of electronic & hard analytical data of raw material / finish product / stability
  • Review & participate in lab investigation (OOS / OOT / Lab events)
  • Review of Audit trail
  • Online review of laboratory compliance
  • Preparation and review of Risk assessment
  • Preparation & review of analytical review data of Finish product / stability.
  • Knowledge of current FDA Guideline

You may give reference of your friends / Ex-Colleagues, in case they meet the requirement mentioned above.


Apply Online Here


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