🚀 Join the Quality Assurance Team at Piramal Pharma Solutions! 🌟
Are you detail-oriented, passionate about quality systems, and ready to make an impact in the pharmaceutical world? 💊 Join Piramal Pharma Solutions and contribute to the development of safe, effective, and high-quality products delivered across the globe.
If you hold a B.Pharm or M.Pharm degree and are looking to elevate your career in Quality Assurance, this is your moment!
🧬 Who We Are
With over 30 years of innovation and excellence, the Piramal Group has grown into a global force in healthcare, known for ethical practices and sustainable development.
Piramal Pharma Solutions (PPS) is a globally integrated Contract Development and Manufacturing Organization (CDMO), serving clients from early-stage drug discovery to commercial production. With facilities in North America, Europe, and Asia, we provide:
Comprehensive pharmaceutical development & manufacturing solutions
Specialized services in biologics, sterile manufacturing, and high-potency compounds
Expertise in small molecules, peptides, antibody-drug conjugates, and more
🔍 Position: Quality Assurance Associate
📝 Key Responsibilities
Develop and maintain the Validation Master Plan (VMP)
Prepare validation protocols and reports for processes, computer systems, and cleaning procedures
Create qualification and requalification documents for equipment, utilities, and facilities
Draft and review protocols for area validations
Conduct and review quality risk assessments
Evaluate calibration records from both internal and external sources
Oversee the Batch Manufacturing & Packaging Records lifecycle – creation to archival
Manage batch record storage, retrieval, and secure disposal
Compile Annual Product Quality Reviews (APQR)
Ensure line clearance for manufacturing, packaging, and dispensing operations
Supervise sampling of bulk and finished goods
Review production documents and verify final product readiness
Monitor deviations and implement Corrective and Preventive Actions (CAPA)
Handle Change Controls, incidents, and support resolution and implementation
Maintain and update QA Standard Operating Procedures (SOPs) using DCS (ENSUR 4.2)
Provide and coordinate employee training as per the training calendar
Support self-inspection programs and monitor compliance
Collaborate on regulatory documentation for dietary supplements (e.g., 21 CFR Part 111 for US markets)
Uphold data integrity, sanitation standards, and EHS guidelines
Coordinate with other departments to support internal and external audits and inspections
🎓 Qualifications
Degree in Pharmacy (B.Pharm or M.Pharm)
Prior experience in pharmaceutical QA is advantageous
Strong understanding of GMP, regulatory compliance, and documentation practices
💼 Why Piramal?
🌐 Global Exposure: Be part of a leading CDMO serving customers worldwide
🤝 Inclusive Culture: We’re proud to be an Equal Opportunity Employer
🚀 Career Growth: Work with cross-functional teams and access continuous learning
🛡️ Ethical Work Environment: Our values are rooted in integrity, excellence, and responsibility
🌍 About the Team
At Piramal Pharma Solutions, we believe in collaboration, innovation, and quality without compromise. We partner with both global innovators and generic players, offering customized solutions for every stage of the pharmaceutical lifecycle—from discovery to commercial production.
📢 Ready to Make an Impact?
This is your chance to join a company where your work truly matters. If you're passionate about quality and want to contribute to global health and safety, apply now and take the next big step in your career with Piramal Pharma Solutions! 💼💡
Apply Link :- https://hcwf.fa.ap1.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1005/job/7876?utm_medium=jobshare
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