Sr. Quality Systems Engineer

Reposted 2 Months Ago
Be an Early Applicant
Devens, MA, USA
In-Office
90K-124K Annually
Mid level
Software • Industrial
The Role
Maintain and improve the Quality Management System (QMS) to meet regulatory requirements; write and control QMS documentation; support NCR, CAPA, internal audits, management review, training, and quality metrics; lead quality system projects and support audits/inspections to ensure compliance and continual improvement.
Summary Generated by Built In

About Us

Founded in 2015 to develop the world’s first industrially scalable laser metal additive manufacturing solution, VulcanForms is reshaping how the world manufactures critical products. We build and operate advanced digital infrastructure that enables innovation, accelerates growth, and supports sustainability across aerospace, defense, medical, and other essential industries. Through our vertically integrated capabilities, including scalable additive manufacturing and precision machining, we deliver true end-to-end production at scale by combining cutting-edge technology with a foundation of proven industrial craftsmanship. Our team brings deep expertise in manufacturing, materials science, software, automation, and operations, united by a shared commitment to quality, curiosity, and accountability. We foster an inclusive culture where people take ownership, solve meaningful problems, and continuously learn, because we believe diverse perspectives lead to better outcomes.

Job Purpose

As a Senior Quality Systems Engineer, you will be responsible for ensuring the QMS is established and maintained in accordance with applicable industry requirements. A candidate must have knowledge of quality systems, CAPA, internal audit, and document control. This position is responsible for writing and updating QMS procedures and is accountable for ensuring the NC, CAPA and internal audit programs are defined and executed compliantly. QMS compliance will be met by ensuring that activities previously noted are conducted according to prescribed procedures, policies, and regulations.


Key Responsibilities

  • Ensure that the Quality System is established and maintained to the highest levels of accordance with applicable regulatory requirements
  • Write, review, and approve the release of changes to QMS documentation
  • Support the NCR program
  • Support the internal audit program
  • Support the CAPA program
  • Support the preparation of Management Review
  • Support the QMS training program
  • Work with other functions to ensure accurate, complete, and efficient change processing and document control activities
  • Prepare and deliver QMS training
  • Support the tracking and trending of quality metrics/KPIs (e.g., CAPAs, NCs, SCARs, complaints, deviations, internal audit findings, calibration and PM, etc.)
  • Identify areas of improvement through data-driven trending and brings solutions to management
  • Lead/support significant Quality System projects effectively
  • Develop innovative and practical solutions to complex and unique process problems and system improvement through the use of best practices
  • Identify/escalate any compliance issues and their potential impact and provide potential solutions/actions so that they can be effectively resolved
  • Support audits and inspections as needed (e.g., coordinate preparation activities, FR/BR support, track resolution activities)
  • Lead or support additional projects as assigned by QA/RA Leadership
  • Support/execute other QMS elements as needed


Qualifications

  • 5+ years experience working in a regulated field with experience in quality systems
  • Experience in writing QMS procedures
  • Experience in NCR and CAPA
  • Excellent communication, interpersonal and leadership skills
  • Experience working with and evaluating Quality metrics and KPIs


Preferred Qualifications

  • Experience with Start-ups
  • Experience in audit support
  • Experience leading and influencing across functional groups and leadership levels
  • Working knowledge of ISO 13485, ISO 9001, and AS9100


VulcanForms offers a competitive salary and equity package. Actual compensation is based on factors such as the candidate's skills, qualifications, and experience. In addition, VulcanForms provides comprehensive benefits including medical, dental, vision, and life insurance; generous paid time off; and a 401(k) plan with company match. 


The annual base salary range for this position is $90,104 to $123,893. 


Skills Required

  • 3+ years experience in medical device or aerospace fields
  • Experience with FDA regulatory requirements
  • Knowledge of ISO 13485 and/or AS9100/ISO 9001
  • Experience writing QMS procedures
  • Experience with NCR and CAPA processes
  • Experience working with and evaluating quality metrics and KPIs
  • Excellent communication, interpersonal, and leadership skills
  • Experience with start-ups
  • Experience in audit support
  • Experience leading and influencing across functional groups and leadership levels
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The Company
HQ: Fort Devens, Massachusetts
189 Employees

What We Do

VulcanForms builds and operates advanced digital manufacturing infrastructure that enables the world's critical industries to innovate, grow, and deliver sustainable impact. A MIT-born company, VulcanForms has invented and commercialized the world’s first industrially scalable metal additive manufacturing (AM) solution and pioneered integrated digital production systems. Combining breakthrough technologies in additive and subtractive manufacturing, industrial automation, digital thread and engineering expertise, the company serves leading medical, defense, aerospace, and semiconductor companies, producing precision components and assemblies. For more information, visit www.vulcanforms.com.

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