What are the responsibilities and job description for the Principle Quality Assurance Compliance Specialist position at piramalpharma?
Be the First to Apply Division Piramal Critical Care 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. For more details, please visit https://www.piramalcriticalcare.com/global/ Job Title Principle Quality Assurance Compliance Specialist Job Description 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. Essential Duties and 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 May require up to 25% travel. Introduce yourself to our recruiters and we'll get in touch if there's a role that seems like a good match. Piramal Pharma Limited, offers a portfolio of differentiated products and services through its 17 global development and manufacturing facilities and a global distribution network in over 100 countries. PPL includes Piramal Pharma Solutions (PPS), an integrated Contract Development and Manufacturing Organization; Piramal Critical Care (PCC), a Complex Hospital Generics business; and the India Consumer Healthcare business, selling over-the- counter products. In addition, one of PPL’s associate companies, AbbVie Therapeutics India Private Limited is a JV with AbbVie Inc. and has emerged as one of the market leaders in the ophthalmology therapy area. Further, PPL has a minority investment in Yapan Bio Private Limited. In October 2020, PPL received a 20% strategic growth investment from the Carlyle Group. PPL provides equal employment opportunities to all employees and applicants for employment. It prohibits discrimination and harassment based on race, color, age, sex, religion, national origin or ethnicity, disability status, genetics, protected veteran status, sexual orientation, gender identity, or expression, or any other characteristic protected by applicable law. Our employment decisions are based on merit considering qualifications, skills, performance, and achievements. Equal employment opportunity applies to all terms and conditions of employment, including recruitment, selection, training, social programs, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions.