Production Executive | Abbott | Baddi

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Job Overview

  • Date Posted
    June 1, 2023
  • Location (State / UT)
  • Expiration date
    --
  • Experience
    6 Years, 7 Years
  • Gender
    Any
  • Desired Qualification
    Bachelor Degree, Master’s Degree

Job Description

The following will be the responsibilities of the position holder:

  • Ensure Compliance with laid standards of the current Good Manufacturing Practices.
  • Coordination for installation and qualification of production equipment and compliance to specifications and validated methods.
  • Coordination with supply chain management for monthly planning and materials.
  • Review of standard operating procedure, master documents of production, batch documents, etc,
  • Implementation of Quality Management System as per cGMP and international requirement at all levels of Manufacturing.
  • Training and evaluation of the Technicians and Executives for their qualifications of specific tasks to operate specific equipment.
  • Investigation in case of any process deviation, non-compliance, market complaints, product failure, product recall, and out-of-specification.
  • Ensure that the production records are evaluated and signed by authorized personnel before they are sent to the quality assurance department.
  • Monitoring and control of manpower utilization, yield, waste data, and budget.
  • Organizing the job responsibilities of the technicians as per the daily plan.
  • To exercise effective control over the process variable affecting the quality of the product.
  • To ensure maintenance of production Area and equipment in the state of cleanliness as per the SOPs at all points of time.
  • Compliance with master documents.
  • Continuous monitoring and improving the production output on a daily basis.

In the absence of the position holder, the subordinate Executive / Manager working in the section or authorized designee (as applicable) shall be responsible for day-to-day work.

Experience & Qualifications:

Experience Required:
  • B.Pharm / M.Pharm with 6-7 years of experience in the core Production area.
  • Should have exposure to regulatory audits such as MHRA, USFDA, etc.