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Senior Executive

Cadila Pharmaceuticals·Mumbai

Pay not stated5–8 yrsFull-time
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About the role

Responsible for planning, supervising, and executing quality-control activities for raw materials, intermediates, finished APIs, in-process samples, and stability samples. The role ensures laboratory activities comply with cGMP, GLP, SOPs, data-integrity requirements, and applicable regulatory standards.

What you'll do

  • Plan and supervise routine QC testing of raw materials, intermediates, APIs, solvents, and finished products
  • Titration and wet-chemistry methods
  • Other applicable analytical techniques
  • Review analytical data, calculations, chromatograms, spectra, and laboratory records
  • Ensure testing is performed according to approved specifications, STPs, analytical methods, and SOPs

What you need

  • 5–8 yrs of experience
  • GMP
  • GLP
  • HPLC
  • Documentation
  • Calibration
  • Chemistry
  • M.Sc or B.Pharm or M.Pharm

Good to have

  • Root cause analysis
  • SOP writing
  • Preventive maintenance

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Can I apply
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Pay
Pay not stated
Source
From the company's careers page · today
How to apply
On 8080-Johnson & Johnson Private Limited Legal Entity's site: account needed, ~10–15 min
Early: posted 14 h ago on their own site