Job Description

Followings will be the responsibilities of the position holder :

  • To Prepare, Review and approval of Process Validation, hold time and cleaning validation Protocol and Reports for oral dosage facility.
  • To perform Technology Transfer Data Package review.
  • To assess and the New Products Internalization / Externalization activities.
  • To Prepare and review of SOPs in Darius.
  • Review of Change controls related to new products, Product transfers and changes in process.
  • To execute assigned tasks in SolTRAQs related to Change control and Exception etc. for ODF.
  • To carry out self-inspection as per assigned schedule.
  • To ensure self-training in ISOtrain within stipulated time and impart training to subordinates/cross functional team as per schedule.
  • To ensure compliance of current Good Manufacturing Practices in the Oral dosage facility & to follow GDP with data-integrity compliance.

In absence of the position holder, Manager working in section or the authorized designee shall be responsible for day to day working.


Job Details

Role Level: Mid-Level Work Type: Full-Time
Country: India City: Baddi ,Himachal Pradesh
Company Website: https://www.abbott.com Job Function: Quality Assurance & Control
Company Industry/
Sector:
Hospitals and Health Care

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