Assistant Manager Production | Gufic Group | Navsari

December 8, 2022
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Job Overview

  • Date Posted
    December 8, 2022
  • Location (State / UT)
  • Expiration date
    --
  • Experience
    3 Years, 8 Years
  • Gender
    Any
  • Desired Qualification
    Bachelor Degree, Master’s Degree

Job Description

Roles and Responsibilities

  •  To assess project and resource requirements.
  • To organize relevant training sessions. 
  • To determine the quality control standards. 
  • Responsible for day-to-day production planning and execution as per requirement. 
  • To supervise and evaluate the performance of production personnel. 
  • Organizing workflow to meet specifications and deadlines. 
  • Responsible for staff/ worker distribution, allocation, and arrangement as per production planning. 
  • Responsible for training new joining persons, chemists, workers, operators, and staff for their respective job. 
  • Responsible to review, approving, and implementing departmental SOPs as per current guidelines. 
  • Responsible for monitoring and status of online documentation such as BMRs/ BPRs/ Log books and if any other documents. 
  • Responsible for monitoring production equipment for their performance and zero breakdowns. 
  • Responsible for monitoring of all activities carried out in the production and packaging area. 
  • Responsible for monitoring stage-wise process for product yield. 
  • Responsible for product quality and improvisation of area and equipment. 
  • Responsible for audit preparation, execution, and compliance. 
  • Responsible for monitoring and review of QMS documents, qualification protocols, and other online documents for any implementation of CAPA. 
  • Responsible to update & maintain online departmental documentation. 
  • Responsible to conduct internal audit / self-inspection to ensure compliance with cGMP and other regulatory requirements. 
  • Responsible to inform top management of future requirements of departmental up-gradation necessary for the growth of the organization and to meet regulatory requirements.
  •  Responsible to coordinate with internal as well as external personnel to maintain the cGMP environment. 
  • Any other responsibilities assigned by the HOD.

Desired Candidate Profile

  • Must have work experience in INJECTABLE and Sterile plants.
  • Working experience in handling instruments like Thimonier. Autoclave, PFS, Dual Chamber machine.
  • Should have worked in the Aseptic area of the Injectable plant.
  • Should be Target Oriented.

Qualification: B.Pharma, M.Pharma