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Director Quality

Job in Ogden, Weber County, Utah, 84403, USA
Listing for: Actylis
Full Time position
Listed on 2026-08-03
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, Quality Control - QC Analysts/Managers
Salary/Wage Range or Industry Benchmark: 120000 - 135000 USD Yearly USD 120000.00 135000.00 YEAR
Job Description & How to Apply Below

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Actylis is a global solutions provider with over 75 years of experience, specializing in streamlining the management of critical ingredients and raw materials for our business partners.

We offer both sourcing and manufacturing solutions tailored to meet diverse and evolving needs, ensuring a reliable, agile, and secure supply network. Our commitment to customization allows us to create flexible solutions, whether it’s a unique specification, custom packaging, or tailored logistics strategies.

With deep expertise in quality and regulatory compliance, sourcing and logistics management, analytical services, and R&D support, we reduce complexities and mitigate risks, empowering our partners to focus on growing their business.

In furtherance of that goal, Actylis is seeking new members of the team. This expansion, coupled with a comprehensive benefits package, and opportunities for challenge and growth, make Actylis the ideal place to work and thrive. We hope you’ll consider joining us!

Position Summary

The Director, Quality is responsible for leading all Quality Assurance, Quality Control, Food Safety, Compliance, and Quality Systems activities at the Actylis manufacturing facilities (Ogden & Centerville), Utah. The incumbent serves as the senior quality leader for the site and is accountable for ensuring products are manufactured, tested, released, stored, and distributed in compliance with applicable regulatory requirements, food safety standards, customer expectations, and Actylis Quality Management System requirements.

This role provides strategic and operational leadership for the site's Quality Management System (QMS), Quality Control Laboratory, Master Control platform, supplier quality activities, customer quality support, audit readiness, batch disposition, continuous improvement initiatives, and compliance programs. The Director, Quality partners closely with Operations, Supply Chain, Procurement, R&D/Product Development, Regulatory Affairs, and Commercial teams to drive product quality, operational excellence, and regulatory compliance while supporting business growth.

Responsibilities will include:

Site Quality Leadership

Serve as the senior quality representative for the Utah manufacturing facilities (Ogden & Centerville).

Act as a member of the Site Leadership Team and primary Quality business partner to the Site Director.

Quality Management System (QMS)

Maintain and continuously improve the site Quality Management System.

Ensure effective implementation and oversight of deviations, CAPA, change controls, investigations, risk assessments, document management, training programs, internal audits, management review, and product quality reviews.

Ensure compliance with corporate quality policies, procedures, and applicable regulatory and customer requirements.

Master Control System Ownership

Serve as Site Business Owner for the Master Control Quality Management System.

Ensure effective implementation and utilization of applicable Master Control modules, including but not limited to Document Control, Training Management, Quality Events, Audit Management, and Supplier Management.

Lead process automation initiatives and continuous improvement efforts within the electronic quality system.

Quality Control Laboratory & External Contract Lab Oversight

Provide leadership and oversight of site Quality Control operations, including external contract testing labs.

Ensure laboratory activities comply with approved methods, specifications, procedures, and data integrity expectations.

Product Release & Batch Disposition

Maintain authority for final product quality disposition decisions, consistent with site and corporate procedures.

Ensure timely review and disposition of raw materials, intermediates, batches, and finished products.

Review and approve quality-related investigations and product release documentation.

Food Safety & Regulatory Compliance

Ensure compliance with applicable requirements, including FSMA, 21 CFR Part 117, HACCP, GMP requirements, and customer‑specific standards.

Support regulatory inspections, certification audits, and customer audits in partnership…

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