Zydus Chemistry QC Job Opening - Apply Online

" data-end="1060">Zydus Chemistry QC Job Opening – Apply Online

Zydus Group is inviting applications for the position of ZTMP QC – HPLC or GC at its API manufacturing facility in Ankleshwar, Gujarat. This opportunity is ideal for candidates with a Master’s degree in Chemistry and experience in HPLC/GC analytical techniques. Whether you’re looking to start your career in quality control or already have Zydus experience, this role offers growth, hands-on training, and the chance to work in a world-class pharmaceutical environment.

About Zydus Group:

Zydus Group is a leading Indian pharmaceutical company with a strong global presence. It is renowned for its innovation, quality manufacturing, and affordable healthcare solutions. With facilities that comply with international regulatory standards, Zydus offers excellent career opportunities for professionals across R&D, manufacturing, quality control, and more. The Ankleshwar facility plays a critical role in API production, and is known for its adherence to quality and operational excellence.

Job Details

Division: ANKLESHWAR QC -U1

Job Title: ZTMP QC – HPLC or GC

Location: Manufacturing – API|API Mfg. Ank., Ankleshwar, Gujarat, India

Employee Type: P-P7-Probationer-HO Staff

Experience range (Years): 0

Qualification:

    • MSc Chemistry – 3-6 Yrs Experience.
    • Experience with GC / HPLC Preferred

Experience in Zydus: Min. 12 months

Job Responsibilities

  • Handling of HPLC system / GC
  • Up-keep of all Instrument Usage Log, Inward Register, Training Records etc.
  • Usage of SOPs, Specifications, and STP for In-process, Intermediate, Finish Product, Recovered Solvents, and Cleaning Sample.
  • Handling of LIMS for Receiving of sample along with Intimation Slip for Inprocess, Intermediate, Finish Product, Recovered Solvents, Cleaning Sample and outside sample etc. and testing as per their Specification and STP.
  • To follow the GMP, Safety norms, and adhere to the company’s policy.
  • Attend training classes, i.e., internal and external programs, as per schedule. Usage of SOPs, Specifications, and STP for In-process, Intermediate, Finish Product, Recovered Solvents, and Cleaning Sample.
  • Receiving of sample along with Intimation Slip for In-process, Intermediate, Finish Product, Recovered Solvents, Cleaning Sample, and outside sample, etc., and testing as per their Specification and STP.
  • After analyzing and writing analytical data, hand over the raw data to a senior person for review.
  • Timely reporting of results and investigation of any deviation, OOS, or incident. Maintain housekeeping and GLP in the working area.
  • Additional Job activities endorsed by the Superior.

APPLY ONLINE HERE

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