"Alerted.org

Job Title, Industry, Employer
City & State or Zip Code
20 mi
  • 0 mi
  • 5 mi
  • 10 mi
  • 20 mi
  • 50 mi
  • 100 mi
Advanced Search

Advanced Search

Cancel
Remove
+ Add search criteria
City & State or Zip Code
20 mi
  • 0 mi
  • 5 mi
  • 10 mi
  • 20 mi
  • 50 mi
  • 100 mi
Related to

  • Senior Director, Quality Assurance and Regulatory…

    Unilever (Austin, TX)



    Apply Now

    About Onnit:

    Onnit is an Austin, TX-based supplement company dedicated to supporting everyday heroes—those who need to be fully present and at their best, not only for themselves but also for their families, friends, and colleagues. As a trusted, serious supplement brand, we provide high-quality products with clinically studied ingredients designed to unlock a deeper mind-body connection and enhance both mental and physical performance.

     

    Unlike other supplement brands, Onnit enables strength from within, empowering individuals to operate at their peak every day. Backed by medical professionals, industry experts, and a loyal community, we are rapidly growing while staying true to our mission of total human optimization. Recognized as a _Best Place to Work in Austin_ by the _Austin Business Journal_ , we take pride in fostering a dynamic and purpose-driven environment—and we’d love for you to be part of it.

    JOB SUMMARY

    The Senior Director, Quality Assurance and Regulatory Affairs will lead the company’s quality assurance, quality control, and regulatory compliance efforts for its dietary supplement products. This role is responsible for developing and executing quality systems through the electronic Quality Management System (eQMS), overseeing audits and regulatory inspections, and ensuring adherence to applicable regulations, including 21 CFR Parts 111 and 117. The position will also serve as the primary liaison with regulatory agencies such as the FDA and FTC. In addition to managing day-to-day quality and regulatory functions, this leadership role requires strategic oversight and close collaboration across departments to drive continuous improvement and ensure regulatory readiness.

    KEY RESPONSIBILITIES

    + Serve as the primary system administrator for the eQMS, managing user roles, permissions, workflows, and systemaccess.

    + Manage controlled documents (SOPs, policies, specifications) within the eQMS and oversee document creation,review, approval, version control, and archiving.

    + Facilitates and organizes training matrix as well as training documents for employees on SOPs, documents, forms andGMPs and ensure company-wide compliance training is up to date.

    + Oversee product complaints, including Adverse Event (AE) tracking, investigation, and reporting.

    + Log and track non-conformances, deviations, and CAPA activities; monitor progress to ensure timely completion andeffectiveness checks, analyze trends, and escalate recurring issues as necessary.

    + Conduct internal audits and support third-party, FDA, and regulatory inspections.

    + Generate and analyze quality KPIs and trends and present quality data for management reviews and continuous improvement initiatives.

    + Collaborate with R&D, Product Development, Marketing, Legal, and Operations to support product innovation andgo-to-market strategies.

    + Advise executive leadership on quality and regulatory risks and opportunities.

    ADDITIONAL RESPONSIBILITIES

    + Maintain inspection readiness through accurate and up-to-date quality records

    + Oversee quality control and quality assurance processes, including finished product release.

    + Collaborate with production, R&D, procurement, and regulatory teams to ensure quality objectives are met.

    QUALIFICATIONS

    +  Develop and deliver training on eQMS usage, GMP, and quality processes to internal users

    + Lead the incident management process, ensuring timely identification, investigation, resolution, and documentation ofquality-related events.

    + Strong understanding of FDA regulations (21 CFR Part 111/117) and GMP requirements

    + Proficiency in Microsoft Office; familiarity with data visualization tools a plus

    + Experience with eQMS platforms

    + HACCP, PCQI certifications (optional, but preferred)

    + Experience with FDA inspections

     

    Onnit takes into consideration a wide range of factors that are utilized in making compensation decisions including, but not limited to, skill sets, experience and training, licensure and certifications, qualifications and education, and other business and organizational needs. This position is bonus eligible and employees are eligible to participate in our benefits plan. Should the employee choose to participate, they can choose from a range of benefits to include, but is not limited to, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, sick leave, paid vacation and holidays. Any coverages for health insurance will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents.

     

    USA Pay Range

     

    $175,000—$200,000 USD

    Benefits

    + Full medical, dental, and vision benefits

    + Basic Life Insurance

    + Immediate 401(k) eligibility with company matching

    + Unlimited vacation

    + Paid holidays

    + Flexible workplace policy

    + $100/month flexible benefit stipend

    + Tuition reimbursement

    + Fringe benefits include in-office meals, product credits and discounts, lifestyle spending account, family planning, online learning, fitness stipend, among many others

     

    EOE race/color/religion/sex/sexual orientation/gender identity/national origin/disability/veteran status

     


    Apply Now



Recent Searches

  • Project Manager Data Technology (New Jersey)
  • Sr Security Consultant Penetration (Nebraska)
  • Senior Lead Solution Architect (Rhode Island)
  • ServiceNow Discovery Admin (Texas)
[X] Clear History

Recent Jobs

  • Senior Director, Quality Assurance and Regulatory Affairs
    Unilever (Austin, TX)
  • Nursing Instructor Adjunct / Temporary Part-Time
    Minnesota State (Minneapolis, MN)
  • Oncology Data Specialist Days Contract $43.40/hr.
    AdventHealth (Daytona Beach, FL)
  • OPIS Senior Database Administrator
    Dow Jones (New York, NY)
[X] Clear History

Account Login

Cancel
 
Forgot your password?

Not a member? Sign up

Sign Up

Cancel
 

Already have an account? Log in
Forgot your password?

Forgot your password?

Cancel
 
Enter the email associated with your account.

Already have an account? Sign in
Not a member? Sign up

© 2025 Alerted.org