Assistant Manager, Quality Control

Par Pharmaceuticals

Par Pharmaceuticals

Quality Assurance
Indore, Madhya Pradesh, India
Posted on Dec 17, 2024

Job Description Summary

The incumbent is required to perform analytical document review in QC.

Job Description

  • To review analytical data of Water Samples Report, Raw Materials, Packing Materials, Stability, Finished Products, In process, Hold Time Studies, Cleaning Samples, Qualifications, Analytical method validation and method transfer samples Report etc. as per the specifications/STP/Protocol etc.
  • To prepare / review of documents (SOP, Protocol, Format, STP, Specification, GTP, work sheet, COA) in VEEVA software as whenever required.
  • To review the daily as well as schedule calibration data.
  • To review the Standard Consumption and HPLC/GC Columns usage etc. in Star LIMS.
  • Responsible to initiate the incident, deviation, investigations, OOS/ OOT etc. and provide support for timely closure of events.
  • Responsible for review of electronic data and sign off activities in software on timely manner wherever applicable.
  • To review logbooks and related documents in laboratory w.r.t the entries made during the material/product analysis.

Commitment to Diversity, Equity, and Inclusion:

At Endo, our diversity unites and empowers us as One Team, and we are committed to cultivating, and valuing, each person’s unique perspective. We actively promote a culture of inclusion that draws strength from our broad spectrums of diversity, including race, ethnicity, religion, gender identity or expression, national origin, color, sexual orientation, disability status, age, and all our other unique characteristics, qualifications, demonstrated skills, achievements, and contributions, backgrounds, experiences, cultures, styles, and talents.