Quality Control Associate

Verdure Sciences
Noblesville, IN

Role at a Glance

Employment Type: Full-time | Department: Quality | Reports to: Director of Quality


Experience Level: 1–3 years hands-on QC experience in a manufacturing environment ( preferably nutraceutical, food, animal health or pharmaceutical).


Work Location: Onsite – Noblesville, IN; Travel: 0-10%.


About Verdure Sciences

For nearly three decades, Verdure Sciences has been pioneering botanical ingredient excellence. From our sustainable sourcing partnerships to our branded ingredients like Longvida® Curcumin and Pomella® Pomegranate, our partners—global consumer brands—trust our commitment to botanical integrity and quality.


You will be a key member of our Quality team ensuring that every batch meets specifications, regulatory requirements, and customer standards. The focus is practical, day-to-day QC execution: coordinating testing with contract labs, reviewing data for release, and maintaining right-first-time documentation under cGMP.


We are specifically prioritizing candidates with hands-on QC experience in manufacturing environments.


Key Responsibilities

• Prepare samples and coordinate testing with qualified third‑party labs aligned to customer specifications and QC test plans.


• Review physical, chemical, and microbiological data; resolve discrepancies and confirm compliance to specifications for batch release.


• Generate Certificates of Analysis (CoA), verify labels, and execute batch release documentation with right‑first‑time accuracy and communicate with suppliers.


• Manage traceability, retains, and stability program records (sampling plans, storage, pulls, and data trending).


• Support in‑house testing routines as needed.


• Maintain document control: specifications, test methods, SOPs, and change control records.


• Participate in quality events: nonconformances, investigations, CAPA/VCAR creation, and effectiveness checks.


• Partner cross‑functionally (Supply Chain, R&D, Sales/Account teams) to resolve issues and meet customer quality expectations.


• Assist with internal/external audits (e.g., NSF, USP, Organic, Non‑GMO) and vendor/contract lab qualifications.


• Stay up to date with industry regulations and best practices related to botanical ingredients and dietary supplements.


What You’ll Bring (Required)


• Bachelor’s degree in a scientific discipline (Chemistry, Biology, Food Science or similar).


• 1-3 years of paid, hands‑on QC experience in dietary supplement, food, animal health or pharmaceutical manufacturing.


• Working knowledge of cGMP (e.g., FDA 21 CFR 111) and quality systems (deviations, CAPA, change control, data integrity).


• Experience reviewing third‑party lab reports and in‑house data; confident interpreting common analytical and microbiological methods.


• Proficiency creating CoAs and maintaining controlled documents; strong attention to detail and organization.


• Fluency with Microsoft Office and Adobe.


• Clear, professional communication skills and a collaborative approach with vendors and internal teams.


Preferred experience:

• Direct experience with dietary supplement/botanical regulations and audits (NSF, USP, Organic, Non‑GMO).


• Qualifying and managing third‑party labs; vendor performance monitoring.


• Statistics/data trending for QC (e.g., control charts, out‑of‑trend checks).


• Electronic quality/document systems and CRM systems (TrackWise, Veeva, SharePoint, Hubspot).


Work Environment & Schedule

Onsite at our Noblesville, IN office/lab | Monday–Friday, 8:30 a.m.–5:30 p.m.


Our Hiring Approach

Verdure Sciences is an Equal Opportunity Employer. We consider all qualified applicants without regard to protected characteristics and provide reasonable accommodation as required by law.


If you bring experience from botanical extracts, herbal ingredients, or plant-based nutraceuticals and have a discovery mindset for innovative quality solutions, we'd love to connect. This is your opportunity to make a meaningful impact in an industry where quality genuinely matters.

Work authorization: Applicants must be currently authorized to work in the United States on a full‑time basis.


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