Production Head | Indoco Remedies | Panaji, Goa

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Job Overview

  • Date Posted
  • Location (State / UT)
  • Expiration date
  • Experience
    18 Years, 20 Years
  • Gender
  • Desired Qualification
    Bachelor Degree, Master’s Degree
  • Salary in (₹)
    19,00,000 - 25,00,000

Job Description

  • Maintain discipline, honesty, and dignity so as to maintain harmony and a good working atmosphere at the workplace. Respect all colleagues.
  • Monitoring & Controlling Production activity on a daily/weekly/monthly basis including dispensing, manufacturing and packing.
  • Ensure availability of necessary change parts, Tooling, replacement of damaged tools & updating affected documents, etc.
  • Handling and Controlling necessary manpower required for the shift to meet daily production targets.
  • Ensure that room conditions like temperature; Relative humidity, pressure differential, etc are monitored for all core and noncore areas.
  • Ensure that all SOPs are followed
  • Ensure that all production accessories, and equipment are properly maintained and cleaned and appropriate status labels are displayed
  • Coordinate with other cross-functional departments like QA, QC, Engineering, and Warehouse Purchase for timely availability of material, equipment, documentation & analytical data.
  • Ensure preventive maintenance is done as per predefined schedules.
  • Ensure calibration status of all the equipment and instruments used in the production area.
  • Ensure online completion of Batch and other in-process documents related to manufacturing and packing activity.
  • Impart periodic training for the subordinates.
  • Ensure that all safety precautions are followed during manufacturing and packing activity.
  • Ensure qualification of new equipment is performed before its release for use.
  • Ensure process, cleaning validations are performed as per VMP.
  • To authorize the RM and PM dispensing work orders, BMRs, BPRs & Departmental SOPs
  • Participation in management reviews of process performance, product quality, and quality management system and advocating the continual improvement
  • To review and assess change controls, deviation & noncompliance’s; if any.
  • To investigate deviations along with the QA head
  • To investigate OOS/OOT for production-related discrepancies, if any.
  • To review and investigate the market complaints.
  • To ensure implementation of data integrity principles.
  • To review the departmental equipment/ Instruments qualification/ requalification documents.
  • To review user requirement specification documents & the departmental equipment.
  • To review risk assessment Protocol documents.
  • To authorize the documents in absence of the site Head.
  • To manage employees working in the department and understand skills and plan improvement in individual functions.
  • To understand the importance of data integrity & its principles & ensure that the same is strictly followed.
  • To ensure that all personnel works proactively to achieve the required goods.
  • To execute planned product at the site as per laid down requirements in batch records.
  • To develop review skills about department functions.
  • To ensure that the handling of solvent is done properly.
  • Co-Ordination with Packaging and Purchase for development of packing materials.

Qualification: B.Pharma, M.Pharma