Job Description

Job Description

  • Review analytical data for Raw Materials (RM), Packaging Materials (PM), in-process samples, Finished Products (FP), stability samples, working standards, reference standards, and other test samples.
  • Review and approve Certificates of Analysis (COAs) for RM, PM, in-process samples, FP, stability working standards, reference standards, and other test samples. samples.
  • Review SOPs, STPs, specifications, and other laboratory documents.
  • Verify the accuracy of data entered in LIMS and manual documentation systems.
  • Review protocols and reports related to analytical method transfer, validation, verification, and waiver activities. Review analytical raw data associated with method transfer, validation, and verification studies.
  • Review and approve daily verification, calibration, and qualification records of laboratory instruments and equipment.
  • Review and approve Computer System Validation (CSV) documents.
  • Review instrument logbooks, calibration records, and third-party calibration reports.
  • Review and approve the audit trail reports for Empower and non-CDS systems.
  • Review stability schedules, stability protocols and stability reports.
  • Ensure data integrity and compliance with ALCOA principles and documentation practices. Verify analytical records for compliance with GLP and cGMP requirements.
  • Review investigations related raw data and report i.e. OOS, OOAL/OOT, deviations, incidents, and change controls.
  • Review vendor qualification reports and related documentation.
  • Review reduced testing reports and related documentation.
  • Review analytical data and COAs received from contract testing laboratories.
  • Review and approve preparation records of reagents, mobile phases, diluents, impurity solutions, and other laboratory solutions.
  • Review analytical raw data for analyst qualification and approved.
  • Verify compliance of laboratory activities through documentation review.

Additional Responsibilities

QUALIFICATIONS

Education

  • B. Pharm B. Pharm - Required
  • M. Pharm M. Pharm - Preferred

Experience:

  • 5 years or more in 5 - 8 Years

Specialized Knowledge: Licenses:


Job Details

Role Level: Not Applicable Work Type: Full-Time
Country: India City: Ahmedabad ,Gujarat
Company Website: http://www.amneal.com Job Function: Quality Assurance & Control
Company Industry/
Sector:
Pharmaceutical Manufacturing

What We Offer


About the Company

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