Principle Quality Assurance Compliance Specialist
About The Position
Piramal Critical Care (PCC), a business unit of Piramal Pharma, is the fourth-largest producer of inhaled anesthetics and a global player in hospital generics. We are motivated by our vision of commitment to delivering critical care solutions for patients and healthcare providers across the globe while achieving sustainable and profitable growth for all the stakeholders. PCC maintains a wide presence across the US, Europe, and more than 100 countries across the globe. Its rich product portfolio includes Inhalation Anesthetics such as Sevoflurane, Isoflurane and Halothane as well as Intrathecal Baclofen therapy, for spasticity management. PCC has a strong manufacturing and process development experience with wholly-owned, state-of-the-art manufacturing facilities in the United States and India, inspected periodically by the US FDA and the UK MHRA and other regulators. The strategic locations of our facilities help us supply high-quality products around the world, timely at optimal costs. Provides continuous oversight of all daily Quality activities to assure compliance with internal procedures and regulatory requirements. Provide proper control, review, and management of site documentation to ensure GMP and regulatory compliance.
Responsibilities
- Responsible for the review, approval, and disposition of finished product for the site and final CoA signature
- Facilitates client project management as required ensuring “quality on time and in full”
- Coordinates the investigation and closure of non-conformances ensuring appropriate corrective and preventive actions (CAPA) and change controls are initiated and deviations are closed
- Leads or participates in focused deviation cross-functional investigations, improvement projects
- Reviews and approves laboratory investigations in a timely manner and ensures appropriate root cause is identified
- Provides assistance to other QA associates and assist with department trainings
- Provides support to QA management during regulatory audits
- Reviews BOMs, inspection plans, pallet patterns, calibration records and SOPs
- Performs internal audits and assist in writing reports for audits
- Maintains and revises procedures related to the quality assurance activities.
- Supports Annual Product Review (APR) reports by collecting batch record data, creating and maintaining data bases
- Maintain the vendor complaint process
- Maintain, monitor and provide trend analysis of DIs, LIs, CAPAs, customer complaints and change controls
- Performs special projects and/or assignments as indicated by Quality Management
- Oversee and review of Obsolete material destruction
- Perform Quality inspections on packaging line as needed
- Maintain supplier approval program
- Support/Maintain site Document Control System
- Review, approve and close out Document Change Requests
- Tracking of changes using DCC spreadsheet and supporting actions through closure
- Maintain original documentation archive and Archival of documents offsite
- Printing of new and revised documents, Issuance of forms, logbooks
- Review documentation submitted for routing in eDMS for proper formatting and accuracy.
- Load documents into an electronic Documentation Management System (eDMS)
- Route documents for approval in the eDMS
- Recall documentation for audits in a timely manner
- Performs external audits and assist in writing reports for audits
- Responsible for maintenance and revision procedures related to document control
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
