Manager/ Sr. Manager - Quality(Document, Data Review & Creation- LIMS)

• Preparation of Master Build in LIMS.
• Oversee track-wise operations for QMS activities.
• Preparation and review of Method Validation, Method Transfer, Method Verification, and Equivalency documents.
• Preparation and review of Test Methods, STPs, and Specifications.
• Operational knowledge of eDMS and ensure application compliance.
• Monitor compendial changes and prepare evaluation reports (including specifications and methods) for affected site products and materials.
• Review analytical data, raw data, chromatography, and LIMS for RM/PM/FP.
• Prepare and review new SOPs.
• Ensure timely completion of documentation.
• Maintain data integrity while preparing, uploading, or reviewing documents.
• Collaborate effectively across Piramal Plants.
• Provide support to any PPL site as required, with role assignments based on evolving needs and timelines.
• Perform activities across US, Canada, and EU time zones; available to travel for up to 3 months to PPL sites (India and overseas) as needed.
• Perform additional tasks as assigned by the Leadership team based on requirements

Experience:

• Hands-on experience in Laboratory software's, testing, applications and systems (Chromatography By HPLC and GC, UV, IR, Dissolution, Malvern, KF auto titrator, etc).
• Must have worked in LIMS for Data entry / master build, and data review.

Shift : As per US, Canada and EU time zone.