workday
Posted 8 weeks ago
Executive-QA
Job description
Be the First to Apply Division Piramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia. This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide. For more details, please visit : www.piramalpharmasolutions.com Job Title Executive-QA Job Description Responsible for managing QA documentation, ensuring GMP compliance, and supporting quality systems through effective handling of SOPs, BMR/BECR review, validation and qualification activities. Oversees document control, vendor qualification, calibration and maintenance coordination, and ensures timely closure of deviations, change controls, and CAPAs while maintaining data integrity and audit readiness across all QA operations. Issuance, archival and retrieval of documents. Issuance of Control coples to respective dept. Destruction of the GMP documents once the retention term has passed and controlled coples of the obsolete GMP documents. Tracking of all QA documents. 5. Maintaining backup of QA softcoples. Maintaining SOP/s with proper indexing. Preparation and review of SOPs Management of QA Stationary (Controlled Coples and logbooks) Dispatch and line clearance activity. Review of BMR/BECR Perform Qualification for new Equipments/Existing Equipments Ensure & Co-ordination of area validations. Reviewing of calibration /PM Schedules. Preparation of VMP &validation Documents Handling of Vendor Qualification Activities. Any other work assigned by HOD/Second line. Involving in handling Deviations, Change Control and related CAPAS. To ensure data integrity compliances while performing activities 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.