Vikrant Singh Parmar

About Vikrant Singh Parmar

As a Global Quality leader, I specialize in fortifying the bridge between complex manufacturing and uncompromising regulatory standards. My focus is on transforming Quality from a reactive function into a proactive competitive advantage. With 20 years of hands-on experience in the Quality domain, specifically in Parenteral and Oral dosage forms, I have honed a profound understanding of critical quality investigations Quality remediation, encompasses expertise in Lab and Manufacturing investigations, Data Integrity Assurance, Quality Management System, Quality System Remediation, Document Management, Quality Operations, Validation/Qualification, Audit and Compliance, Quality Lab Assurance, IT Compliance, and Training.Management of Global Critical Quality Investigations, encompassing the evaluation of FAR or HA notifications, I am an experienced professional characterized by a robust work ethic and unwavering self-accountability.My leadership capabilities have been demonstrated through proven success in providing guidance, training, and mentorship to teams. This has resulted in improved communication, enhanced collaboration, and the strategic addressing of compliance gaps and elimination of non-compliances. I excel in managing potential data integrity breaches, ensuring the alignment of IT processes with compliance standards, and developing comprehensive training programs.In summary, I bring a wealth of experience and subject matter expertise to the table, coupled with a track record of successful leadership. My goal is to foster a culture of compliance, continuous improvement and achievement of both business and quality objectivesI am driven by results and thrive in dynamic environments, showcasing strategic leadership and a wealth of comprehensive quality management experience acquired through a blend of functional expertise, specialized training, and exposure to diverse challenges and developmental opportunities. My management style prioritizes employee empowerment and effective interpersonal communication.My proficiency extends to a profound understanding of regulatory requirements and international standards, such as CFR Title 21 Parts 11, 210, 211; EudraLex Vol. 4; WHO; GAMP; PDA; ICH; and PMDA. This knowledge underscores my commitment to ensuring compliance and upholding the highest quality standards within the pharmaceutical industry. Gained valuable work experience with NSF, Lachman,PwC, and PQE Consultants for Quality system remediation.This dedication cornerstone of our team\'s success in advancing Global Quality domain

Experience

1. General Manager-global Quality

   Viatris

   Mar 2026 — Present · Hyderabad, IN

   General Manager - Global Quality @ Viatris ​Leading the charge in Global Quality Strengthening and Data Integrity across a diverse portfolio of Sterile and Non-Sterile products. My mission is to move the needle from compliance to Quality Excellence through:​ Investigation Excellence – Deep-dive RCA and sustainable CAPAs. Remediation Leadership – Rapid, thorough response to complex quality challenges. Proactive Quality Management – Building resilient systems that anticipate risk. Strategic CQN Investigation – Safeguarding patient safety and brand reputation.​#Sterile #NonSterile #DataIntegrity #Remediation #GlobalCompliance #QualityExcellence #Viatris #PharmaceuticalLeadership

Education

• B.U.Jhansi

  Master of Science, Organic Chemistry

  2003 — 2005

Skills

• Quality Control
• Gmp
• Quality System
• Quality Assurance
• Validation
• Capa
• Technology Transfer
• Anda
• Regulatory Submissions
• Pharmaceutics
• Computer System Compliance
• Audit Committee
• Glp
• Regulatory Requirements
• Pharma Compliance
• Training
• Testing
• Regulatory Affairs
• Pharmaceutical Industry
• Sop
• Fda
• Laboratory
• Troubleshooting
• Standard Operating Procedure (Sop)