Trainee - Quality Control

Piramal Pharma Ltd

Thane

On-site

INR 180,000 - 240,000

Full time

9 days ago

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Job summary

Piramal Pharma Ltd in Navi Mumbai invites applications for a QC – Trainee to join our Quality Control team. The role focuses on developing and executing QC schedules aligned with global demand and available capacity.

You will perform sampling and analysis of Raw Material, Packing Material, Inprocess & Intermediate Samples, and assist in the operation and calibration of QC instruments (KF, UV, HPLC, GC, pH meters, etc.).

Qualifications

  • Degree in chemistry or related field (Masters/ Bachelor's).
  • Full-time position.

Responsibilities

  • Sampling and analysis of Raw Material, Packing Material, Inprocess & Intermediate Samples.
  • Operation and calibration of QC instruments including KF, UV, HPLC, GC, pH meter, and others.
  • Sampling and analysis of water samples.
  • Maintain documentation as per cGMP requirements.
  • Assume reporting authority in the absence of supervisor.

Skills

Sampling
Analysis
Instrument calibration
Documentation

Education

Bachelor's degree in Chemistry
Master's degree in Chemistry

Tools

KF
HPLC
GC
UV spectrophotometer
pH meter
Coulometer
Oxygen gas analyzer
Melting point apparatus

Job description

Job Description

Trainee - Quality Control Business: PPL Department: Quality Control Location: Navi Mumbai Travel: Low Job Overview We are looking for a QC – Trainee to join our team. The role will be responsible for developing and executing Quality control schedules in alignment with global demand and available capacity.


Key Responsibilities


  • Sampling and analysis of Raw Material, Packing Material, Inprocess & Intermediate Samples

  • Operation and calibration of QC Instruments like KF. Melting Point. Potentiometer, Coulometer, Conductivity meter, Refractive Index, UV. GC, HPLC, Boiling Point, pH meter, TOC, Analytical balance, Auto Polarimeter. Oxygen Gas analyzer, Gastec Pump and Oxygen meter etc.

  • Sampling and analysis of water.

  • To maintain the documentation as per the cGMP requirement.

  • To handle the responsibilities of reporting authority in his/her absence.


Masters/bachelor’s degree in chemistry or a related field. Full time

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