Manufacturing Quality Engineer

About Us

The Ammortal Chamber brings together multiple scientifically backed technologies into one experience. It is a healing technology that can be utilized by wellness clinics and inside the home. Our clients include specialty spas and clinics, sports teams, and individuals who are biohackers or athletes.

We are a small team with a startup culture. After our first full year shipping a finished product on the market, we have shown strong growth. Our team is made up of engineers, health professionals, and startup entrepreneurs.

As we continue expanding, this role offers hands-on experience, opportunities to grow into leadership, and the chance to make a tangible impact by developing and delivering cutting-edge wellness technology. You’ll collaborate across disciplines to innovate and shape technologies that enhance well-being for our clients.

What is this role and why does it exist?

Ammortal is rapidly scaling the manufacturing of its Chambers, and a Manufacturing Quality Engineer will ensure our production meets the highest standards as we grow. This role will oversee quality control with our Contract Manufacturer (CM), manage key engineering documents, and drive process improvements to support seamless scaling. Their expertise will be critical in maintaining consistency, efficiency, and compliance as we expand production exponentially.

Responsibilities:

1. Quality Assurance Oversight: Ensure that all Chambers manufactured by the Contract Manufacturer (CM) meet Ammortal's quality standards and regulatory requirements.
2. Documentation Management: Develop and maintain comprehensive engineering documents such as work instructions, quality plans, and manufacturing procedures to guide production and ensure consistency.
3. Supplier and Vendor Quality Management: Collaborate closely with the Contract Manufacturer and other suppliers/vendors to resolve quality issues, implement corrective actions, and drive continuous improvement initiatives.
4. Compliance and Regulatory Adherence: Ensure compliance with relevant industry standards, regulations, and certifications (e.g., ISO standards) to uphold product quality and safety.
5. Process Improvement: Perform studies such as time studies, yield, and materials fallout to identify areas for process optimization and efficiency gains within the manufacturing process to enhance quality, reduce costs, and improve overall production output.

Skills Required

1. Quality Control & Assurance – Deep understanding of manufacturing quality standards, inspection processes, and defect analysis to ensure Chambers meet Ammortal’s high standards.
2. Manufacturing Process Engineering – Ability to optimize production workflows, troubleshoot issues, and implement process improvements for efficiency and scalability.
3. Technical Documentation – Strong skills in creating and managing engineering documents, including work instructions, quality control plans, and compliance documentation.
4. Problem-Solving & Root Cause Analysis – Expertise in identifying, analyzing, and resolving manufacturing defects or inefficiencies using tools like 8D, DMAIC, or Fishbone Diagrams.
5. Collaboration & Vendor Management – Ability to work closely with the Contract Manufacturer, suppliers, and internal teams to ensure seamless production and continuous improvement.

What technical knowledge do you need to perform in your role?

Required

1. ISO 9001 Experience or equivalent – Strong understanding of ISO 9001 quality management systems and ability to implement and maintain compliance in a manufacturing environment.
2. Manufacturing & Quality Engineering Tools – Proficiency in one or more of the following: Six Sigma, Lean Manufacturing, Root Cause Analysis (8D, 5 Whys, Fishbone Diagrams), and/or Statistical Process Control (SPC) to drive quality improvements.

Preferred

• Technical Documentation & CAD Software – Ability to create and manage work instructions, engineering change orders (ECOs), and process documentation. Experience with SolidWorks, AutoCAD, or other CAD software.
• Regulatory & Compliance Knowledge – Familiarity with FDA, UL, CE, and other relevant regulatory requirements depending on product classification and market needs.

Qualifications (Must haves):

• 5+ years managing quality at a manufacturing facility or for a electromechanical device
• Supplier & Contract Manufacturer Quality Management – Experience working with external manufacturing partners, performing supplier audits, process validations, and corrective action management (CAPA).

Qualifications (Nice to haves):

• Experience leading ISO 9001 implementation (or similar ISO standard)
• Experience supporting NRTL listing compliance audits
• IPC 610/620 certified

Pay range: $120,000 - $150,000

• This range is broad because we are considering a broad range of experience levels
• As a generalization,
• If you are in the 2.5-5 years of experience range, expect to be in the first half
• If you are in the >5 years of experience range, expect to be in the upper half

Benefits: 80% health, dental, vision covered

Location: Mars Hill (20 min north of Asheville, NC)

Hours: Flexible, goal-oriented schedule, typically 9-5 Monday to Friday.