Aanchal Sharma

Qa/ra Supervisor at Lief Labs

Aanchal Sharma is a seasoned professional with extensive experience in regulatory affairs and quality assurance, currently serving as a QA/RA Supervisor and Regulatory Affairs Coordinator Lead at Lief Labs since July 2020. Sharma has demonstrated leadership in managing regulatory teams, overseeing third-party certifications, audits, and company licensing, while ensuring compliance with cGMP and GDP guidelines. Proficient in 21 CFR parts 111 and 109, Sharma conducts label reviews and supplement facts panel evaluations. Previous roles include Regulatory Affairs Specialist, where compliance with 21 CFR Part 111 and exporting regulations was emphasized, and QA Specialist at Centene Corporation. Aanchal also holds a Bachelor's degree in Liberal Arts and Sciences/Liberal Studies from California State University, Northridge.

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Lief Labs

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Lief Labs is a premier formulation and product development innovator and manufacturer of dietary supplements. Our in-house Product Development and R&D Team creates the best tasting and most cutting edge formulations for your dietary supplement needs. Lief also houses a state of the art, full-service **cGMP** manufacturing facility, which offers custom solutions for a multitude of dietary supplement categories. At Lief we have the industry knowledge and vision that allows us to stay ahead of trends and recognize opportunities for collaborations with entrepreneurial firms to help them build premier brands that stay relevant well beyond product expiration dates. Lief‘s turnkey solutions provide the ability to streamline operations which integrates with our customers to engage in a seamless partnership that helps brands with scalability, regulations and sustainable growth. With over 15+ years of experience in supplement manufacturing, we offer a wide range of categories that can meet or exceed the national brand standards.


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11-50

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