HomeProductionQuality Control Technician III (MPharma/M.Sc) | Teva Pharmaceuticals | Goa

Quality Control Technician III (MPharma/M.Sc) | Teva Pharmaceuticals | Goa


Teva is a global pharmaceutical leader and the world’s largest generic medicines producer committed to improving health and increasing access to quality Health solutions worldwide.

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Our employees are at the core of our success, with colleagues in over 80 countries delivering the world’s largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we’ve built a promising pipeline centered around our core therapeutic areas. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development, and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

Position: Quality Control Technician  III

Location: Goa, India

Job Description:

  • Analysis, review, and reporting of data, and disposal of stability samples
  • Preparation and standardization of volumetric solutions, reagents and related documentation as in the prevailing Standard Operating Procedures(SOP)
  • Ensure that the currently approved procedures, test methods, stability protocols, and specifications are followed
  • Ensure all instruments are calibrated prior operating
  • Ensure assigned and regular training are taken, completed and training records are maintained

  • Check, review and maintain the logbooks, stability history/trend related to analysis, Certificates of analysis, specifications, test procedures, validation reports
  • Updating Status labels
  • Report to the Superior about the results obtained in routine analysis and assist in performing investigation
  • Ensure correctness of the raw data generated and submitted for review
  • Maintain cleanliness and sanitation in the laboratory
  • Ensure proper and complete documentation in analytical documents, raw data book/ Test Data Sheets, logbooks, chromatograms, instrument prints in compliance to applicable SOP
  • Ensure compliance with the requirements of site procedures on Data integrity in GxP data handling
  • Assist analysts in troubleshooting of instrumental problems
  • Ensure instrument/equipment is within calibration due date prior using of instrument

Qualification: M.Sc/M.Pharma

Experience: 2-4 Years

Salary: Negotiable

Contact Details:

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