PI

Apprentice Trainee - Mechanical

Piramal Pharma Limited
Chennai50K-3 LPA Posted 16 Apr 2025
FULL TIME
Qa
Validation
Cgmp

Job Description

Job description

Description:

  1. Strict adherence to cGMP, Statutory norms and safety rules of the factory 
  2. Taking a role of competent person under the Engg. Sr.Manager and reporting back the progress / Issues on daily basis. 
  3. Prepare the list of equipment's and update the same whenever require in line with the QA
  4. Prepare the annual PM, Validation and qualification schedule of equipment's, ensure the effective implementation in line with SOP
  5. Upkeep the plant and equipment's to ensure any time audit readiness.
  6. Engage the team members in a productive manner.
  7. Manage the contract workers effectively and verify their measurements, billings with actual work done.
  8. Access the critical spares for the equipment's and ensure its availability on time.
  9. Collaborate with the cross functional teams to build consensus.
  10. Take a lead to prepare / update the documents for the ISO audits.
  11. Prepare the monthly global engineering reports. Understand the global engineering standards, identify and explore the gaps, ensure the training to all employees in the department for the approved standards. 
  12. Understand the system, Operation and Procedures identify the opportunities in terms of Energy conservation, overcome the repeated jobs, reduce frequent breakdowns in line with the overall operational excellence.

Required Skills

Join WhatsApp Channel