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jobs:Production Head in Faridabad

jobs:Production Head in Faridabad

Position Title Production Head in Faridabad
Categories Manufacturing/Production/Quality, Pharma/Biotech/Clinical Research
Salary 20 – 35% Hike on CTC
Job New New
Position Summery Designation : Production Head Qualification: Pharma Graduate Experience : 2 to 8 Yrs Salary : 20- 35% Hike on CTC Industry : Pharmaceuticals Manufacturer Location : Faridabad
Start Date 2016-05-13
Location Faridabad
Job Information
Designation : Production Head
Qualification: Pharma Graduate
Experience : 2 to 8 Yrs
Salary : 20- 35% Hike on CTC
Industry : Pharmaceuticals Manufacturer
Location : Faridabad

Job Role & Responsibilities

  • Responsible for preparing Production plans as per monthly plans and implementing on shop floor.
  • Responsible for planning and controlling Manpower for production activity
  • Responsible for job allocation for Executives and Supervisors section wise for executing and Overseeing the production process
  • Responsible for ensuring coordination of Production with Warehouse, Quality Control, Quality Assurance for daily follow ups for material, analysis and documentation respectively
  • Responsible for indent of change parts for the Production equipment and advising Engineering department for procuring spares time to time.
  • To ensure that the products are produced and stored according to the appropriate documentation in order to obtain the required data.
  • To approve the instructions relating to Production operations including the in-process controls and to ensure their strict implementation.
  • To ensure that the Production records (Documentation) are evaluated and signed by a designated person before they are made available to the QA department.
  • To check the maintenance of the department, premises and equipment.
  • To ensure the appropriate process validations and calibrations of control equipment are performed and recorded and the reports made available.
  • To ensure compliance to all regulatory requirements and statutory requirements
  • To participate in internal or external audits as subject matter expert for assigned area
  • To ensure that the required initial and continuing training of Production personnel is carried out and adapted according to need.
  • To ensure the implementation of cGMP, WHO-GMP, ISO Guidelines
  • To ensure the plant’s safety standards are in followed
  • To support safety incident investigation, root cause analysis, and implementation of corrective/preventive actions and continuous improvement initiatives
  • To respond to detailed inquiries and present information to senior management
  • To identify errors or faults in the process and recommend/implement solutions.
  • May perform other duties as assigned

Requirements:

  • Experience in of dosage forms manufacturing / packaging & the processes associated with it (Tablets, capsules in Beta, non-beta sections and other dosage forms)
  • Operational Knowledge of Production Machinery(Manufacturing/ Packaging)
  • Exposure to Regulatory requirements, cGMP Requirements, WHO-GMP, ISO 9001:2008 implementation, MHRA
  • Computer proficiency
  • Manpower Management
  • Good communication and presentation skills

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