Executive/Senior Executive – Quality Control | Alembic Pharma | Vadodara

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Job Overview

  • Date Posted
    April 29, 2023
  • Location (State / UT)
  • Expiration date
    --
  • Experience
    2 Years, 5 Years
  • Gender
    Any
  • Desired Qualification
    Master’s Degree

Job Description

Roles and Responsibilities

  • Analysis of In-process, Intermediates, Raw material, Packing material, Finished products, Stability study, Hold time study, Process validation, Cleaning samples, Vendor development, and any analysis allocated by the team leader and release with proper documentation.
  • Ensuring analysis is performed in compliance with GLP.
  • Ensuring analysis raw data is documented on-line.
  • Initiation, Completion, and filing of Daily analysis reports.
  • Ensuring any abnormal results, incidents, deviations, and discrepancies are reported immediately to the reporting Section Head.
  • Ensuring all relevant log entries are made for every activity wherever applicable.
  • Supervise compliance to all cGMP, GxP, or any other regulatory requirements including EHS requirements.
  • Report any quality concerns or suggestions for improvements to Department Head.
  • Execute and supervise all tasks and activities as per the applicable SOPs and company policy.
  • To maintain the safety norms while working in the lab. (e.g. Wear goggles, PPE, Disposal of sample/media as per procedure, etc).
  • Ensuring analysis is performed as per valid procedures and by using calibrated instruments / Standards.
  • Ensuring self-discipline with respect to wearing aprons, attendance, and personnel hygiene and interrelations.
  • To perform Labware LIMS-related activities.
  • Any other assignment was given by the Section Head or Department Head.

Desired Candidate Profile

  • Qualification: B.Sc,/M.Sc
  • Experience: 1-5 Years of all cGMP, GxP, or any other regulatory requirements

Interested Candidates can Apply with their most recent CTC Break-up