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Natasha Rivas brings over seventeen years of experience in the pharmaceutical and medical device industry, previously holding roles in quality control, quality assurance and regulatory affairs at Abbott, Hospira and Vetter Pharma Fertigung. While at Vetter, Natasha lead teams that focused on ensuring the release of safe and effective product, as well as ensuring timely and transparent communications to meet the needs of her many pharmaceutical customers. Her current responsibilities include providing quality control and quality assurance oversight for SCA’s Windsor, CT facility. Natasha holds a Bachelor of Science in Molecular Biology, is a Certified Quality Auditor through ASQ and is an active member of PDA.

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