Executive

2 - 5 years

3 - 6 Lacs

Posted:8 hours ago| Platform: Naukri logo

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Work Mode

Work from Office

Job Type

Full Time

Job Description

  • Maintain specimen signature logbook and ensure the signature of employees being recorded before starting the work.
  • Prepare training curricula for an employee/ Job Description based on the need in consultation with the Department head and respective reporting manager.
  • Ensure review of training file and LMS report for the completion of trainings, applicable OJT s and certify the trainees post completion of the same.
  • Responsible for updating classroom/ OJT/ awareness training attendances and related data in the LMS.
  • Responsible for archiving of training records of respective departmental employees.
  • Ensures training records of resigned employees are stamped and archived as per the procedure.
  • Creating and uploading SCORM enabled content, learning items, content objects, assessments, tasks, checklists etc. in LMS and assigning/ mapping of cross-functional procedures to users as applicable for all the SOPs/EOPs/IOPs etc.
  • Track and report the due date compliance of assigned trainings for the team/ department in LMS.
  • Responsible for identifying and maintaining the training records of all the approved service providers and contract employees.
  • Involved in the procurement of labels used in GMP facility as per Procedure for Labelling upon user request as per requirement.
  • Involved in the Training certification of Employees as per Training and Certification of Personnel.
  • Involvement in EDMS Activities and Preparation of GMP documents.
  • Issuance, control and Archival of GMP documents such as SOP/EOP/IOP/BMR.
  • Tracking due for review of SOPs and ensuring it s on time review and effectiveness.
  • Ensure preparation of organization charts/ List of employees involved in GMP operations and archiving the same in QA Archival.
  • Ensure timely initiation, Logging and closure of QMS Document Such as Deviation, Change control, CAPA.
  • On-time extensions to be taken before the due date for any QMS documents like Deviation, Change control, CAPA.

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