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ScieGen Pharmaceuticals Hiring For Quality Control

Published on

Quality Control

ScieGen Pharmaceuticals India Pvt. Ltd.

B.Pharm, M.Pharm, B.Sc., M.Sc

Jadcherla, Telangana

2–8 Years

Verified Job

Email Application

ScieGen Pharmaceuticals India Pvt. Ltd. is hiring experienced professionals for Quality Control Executive / Senior Executive positions at its facility in Jadcherla, Telangana. Candidates with 2 to 8 years of experience and qualifications in B.Sc., M.Sc., B.Pharm, or M.Pharm can apply.

The recruitment is for Quality Control professionals with hands-on experience in analytical instruments, laboratory testing, calibration, analytical method validation, documentation, and quality management systems.

Job Details

ParticularsDetails
CompanyScieGen Pharmaceuticals India Pvt. Ltd.
DepartmentQuality Control
PositionsExecutive / Senior Executive
Experience2–8 Years
QualificationsB.Sc., M.Sc., B.Pharm, M.Pharm, or equivalent
Job LocationJadcherla, Telangana
Application ModeEmail

Positions

  • Quality Control – Executive
  • Quality Control – Senior Executive

Job Responsibilities

Selected candidates will be responsible for:

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  1. Following Good Laboratory Practices (GLP), including ALCOA++, and maintaining laboratory upkeep.
  2. Operating analytical instruments such as HPLC, GC, Dissolution, IR, UV, Polarimeter, PSD, pH meter, and analytical balances.
  3. Performing routine chemical and instrument-based analytical testing of RM, PM, IP, FP, and ST samples.
  4. Executing routine calibrations, AMV, AMT, and MT activities.
  5. Reviewing analytical data and audit trails.
  6. Managing laboratory procurement activities and maintaining stock records.
  7. Preparing and reviewing protocols, reports, raw data, COAs, SOPs, specifications, test procedures, records of analysis, and logbooks.
  8. Initiating, investigating, and reviewing QMS activities and reporting them in real time.
  9. Sending samples to external laboratories and maintaining the relevant records.
  10. Working in shifts and maintaining flexibility as required.

Eligibility and Qualifications

Candidates must meet the following requirements:

  • B.Sc., M.Sc., B.Pharm, M.Pharm, or equivalent qualification.
  • 2 to 8 years of relevant experience.
  • Hands-on experience in analytical instruments and laboratory testing.
  • Knowledge of GLP and ALCOA++ practices.
  • Flexibility to work in shifts.

Required Technical Skills

Candidates should have practical knowledge or experience in:

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  • Analytical Instruments: HPLC, GC, Dissolution, IR, UV, Polarimeter, Particle Size Distribution (PSD), pH meter, and analytical balance.
  • Laboratory Testing: Routine chemical and instrument-based analytical testing for RM, PM, IP, FP, and ST.
  • Quality Control Activities: Routine calibration, AMV, AMT, and MT.
  • Documentation: COA, SOP, specifications, test procedures, protocols, reports, raw data, and logbooks.
  • Compliance: GLP, ALCOA++, QMS, and audit trail review.
  • Laboratory Management: Procurement, stock maintenance, and external laboratory sample coordination.

How to Apply

Eligible candidates can submit their updated resume and portfolio to the following email addresses:

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