Quality Control Manager

Job not on LinkedIn

🔥 0 minutes ago

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Supergut

WebsiteLinkedInAll Job Openings

11 - 50 employees

Founded 2019

💰 $22M Venture Round - Supergut on 2025-02

Supergut is a company name provided by the user but there is no information about Supergut in the supplied text. The supplied content appears to be HTML / marketing content for Linktree, not Supergut, so I cannot reliably describe Supergut's business or products from this input. I cannot invent details. Please provide Supergut's website copy, a short summary, or key facts (what they sell, target customers, business model) and I will produce a concise description and pick up to three relevant industries.

📋 Description

• Develop, implement, and continuously improve Supergut’s internal Quality Management System • Create and maintain: Raw material specifications, Finished product specifications, Packaging component specifications, SOPs and quality manuals • Maintain document control processes, revision tracking, and controlled documentation systems • Establish and manage change control procedures • Ensure quality systems always remain audit-ready • Ensure Supergut maintains compliance with dietary supplement cGMP requirements under 21 CFR 111 • Establish and oversee finished product testing and release processes • Review and approve: Certificates of Analysis (COAs), Analytical testing reports, Batch documentation for release verification • Maintain traceability systems and release documentation • Ensure appropriate documentation retention practices are followed • Establish and oversee a compliant finished product retain program • Maintain secure, organized storage of retains (or oversee third-party retain storage facilities) • Track retain inventory and expiration timelines • Conduct periodic organoleptic evaluations of retains as part of ongoing quality monitoring • Qualify and approve contract manufacturers, raw material suppliers, and third-party testing laboratories • Establish and maintain supplier qualification programs (risk-based; primarily paper audits with on-site visits) • Review and manage quality agreements • Conduct supplier performance evaluations • Manage and maintain third-party certifications, including but not limited to: Project Non-GMO, Low FODMAP, Vegan, Gluten Free or other applicable certifications

🎯 Requirements

• 5+ year’s experience in Quality Assurance and/or Regulatory Affairs within dietary supplements • Strong working knowledge of FDA dietary supplement regulations (21 CFR 111) • Demonstrated experience managing third-party certification programs (e.g., Non-GMO Project, Vegan, Low FODMAP or similar) • Experience overseeing finished product testing and release processes • Experience developing and maintaining stability programs • Experience managing retain programs for finished dietary supplement products • Experience managing quality systems across multiple contract manufacturers • Familiarity with analytical testing methods and third-party lab coordination • Bachelor’s degree in Food Science, Chemistry, Biology, or related field

🏖️ Benefits

• Unlimited PTO • 401(k) match • Comprehensive medical, dental, and vision coverage with generous employer contributions