We are a fast-growing dietary supplement manufacturer operating in compliance with 21 CFR Part 111, seeking a hands-on QA/QC professional who is motivated by building, strengthening, and refining quality systems—not simply maintaining the status quo.

This role combines daily QA/QC execution (including raw materials & product receiving, in-process and final reviews for materials / documentation, material quarnatines and releases, and document control) with active Quality Management System development. Responsibilities include writing and reviewing SOPs, MMRs, and BPRs; supporting supplier qualification; strengthening CAPA effectiveness; and contributing to GMP training programs. You will partner closely with Quality leadership to enhance process consistency, reduce errors, and elevate our long-term “inspection-ready” posture.

The ideal candidate is comfortable operating in a dynamic, growing environment and is eager to help establish structure, drive continuous improvement, and ensure those improvements are sustainable.

What you’ll do

Quality System Continuous Improvement

Partner with Quality leadership to identify compliance gaps, prioritize improvements, and execute a practical roadmap across documentation, training, supplier qualification, and CAPA.

Improve how we work by standardizing templates and workflows (SOPs, forms, logs, batch packets) to reduce human error and rework.
Strengthen specifications, acceptance criteria, and review workflows so release decisions are consistent and fast.
Help establish quality metrics (doc errors, deviations, supplier performance, training completion) and drive corrective/preventive actions.

Documentation & Record Control

Draft, revise, and version-control SOPs, Work Instructions, forms, and logbooks; route for review/approval; train teams on changes.
Build and maintain Master Manufacturing Records (MMRs) (21 CFR 111.210) and ensure executed Batch Production Records (BPRs) (111.260) are complete, legible, and compliant.
Support document change control (redlines, impact assessments, training, effective dates).

Quality Control Operations

Perform/coordinate receiving inspections, in-process checks, line clearance, label reconciliation, and finished product release/quarantine per specifications.
Support sampling plans (ANSI/ASQ Z1.4 / ISO 2859), retain management, and reserve samples (111.83).

Supplier & Material Qualification

Maintain the Approved Supplier List; collect/assess questionnaires, audits, and performance data.

Deviations, Investigations & CAPA

Log and investigate deviations/OOS/OOT and drive CAPA through effectiveness checks.
Track trends and propose preventive actions to reduce repeats.

What you’ll bring
Minimum (one of the following)

1+ year in a QA or QC role in dietary supplements or food/beverage.
Relevant education/training (degree in relevant field, GMP certifications, etc.) demonstrating readiness to perform regulated QA/QC work.

Bonus points if you have

Experience supporting regulatory inspections or GMP certification audits.
Experience with Lean Manufacturing / Six Sigma
Experience with cloud-based ERP/MRP platforms.
Experience developing/reviewing product specifications.
Experience developing/reviewing product packaging and labeling.
Solid Excel/Google Sheets skills (filters, pivot tables, lookups) and comfort learning digital tools (we use digital systems and expect you to learn quickly).

Physical & work environment

Stand/walk on a production floor; lift up to 50 lbs occasionally; wear PPE; work around food-grade solvents and flavors.
Adhere to hygiene, gowning, allergen, and sanitation rules.
Must have reliable transportation; role may include traveling between sites.
Must be willing to work early/later than business hours on occasion.

About the company

Sun Nutraceuticals is a contract manufacturer of dietary supplements based in Fort Lauderdale, Florida, with an FDA-registered and cGMP-compliant facility. It provides end-to-end services from formulation and development to production and integrated fulfillment, serving as a single partner from concept to consumer, with private-label and custom formulations. The company makes capsules, powders, gummies, tablets, and liquid shots for categories like sports nutrition, collagen, creatine, and beef organ capsules, and its in-house team develops formulations for new concepts while performing third-party testing with a Certificate of Analysis. Its integrated fulfillment handles direct-to-consumer shipping, Amazon FBA preparation, and B2B distribution from the production site, with MOQs starting at 5,000 units to support early-stage brands.

Company Size

11-50

Company Stage

N/A

Total Funding

N/A

Headquarters

Fort Lauderdale, Florida

Founded

2018

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Simplify's Take

What believers are saying

LinkedIn showed $12 million 2026 revenue pace and 33 employees on September 4, 2026.
August 2026 postings covered QA, maintenance, inventory, and Amazon leadership roles.
Website refreshes in late August and September 2026 signal active sales and product expansion.

What critics are saying

June 2026 QA/QC hiring signals quality systems still scaling during production growth.
BBB lists Sun Nutraceuticals as unrated and not accredited, weakening trust with brands.
One contamination event could halt contract manufacturing and in-house Amazon launches immediately.

What makes Sun Nutraceuticals unique

Fort Lauderdale site combines capsule, powder, label, and fulfillment operations under one roof.
Sun Nutraceuticals runs in-house manufacturing, not brokerage, for custom and private label programs.
5,000-unit minimums and 6-8 week lead times fit emerging supplement brands.

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Benefits

Health Insurance
Dental Insurance

Sun Nutraceuticals

Quality Assurance/Quality Control Specialist - Dietary Supplement Manufacturer

About the job