2,073,754open jobs
126,782companies
241,379added this week
Browse all
Location
In office (Devens)
Seniority
Senior · 5+ years exp

Confirmed on the employer's own hiring board on Nov 3, 2026. First seen by Alion on Nov 3, 2026. Spirax Group scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Solutions for a more efficient, safer and sustainable worldSpirax Group is positioned to play a critical role in enabling the industrial transition to net zero.

The Senior Quality Engineer is responsible for leading, developing, and maintaining the site’s quality validation, product qualification, and risk management programs, ensuring alignment with ISO standards, internal Quality Management Systems, and regulatory expectations. This role supports NPI (New Product Introduction) and Design Development Quality, providing technical oversight and quality governance on all activities including production to ensure product safety, regulatory compliance, and robust validation lifecycle control. Acting as the site’s subject matter expert (SME) in quality validation, risk management, and metrology, the Senior Quality Engineer collaborates with cross-functional stakeholders in Engineering, Manufacturing, R D, Supply Chain, and Quality Assurance to drive consistent, compliant, and effective practices.

Key accountabilities include: Supervise your designated team. Develop, implement, and sustain effective quality management system (QMS) processes, including the creation and control of procedures, templates, and quality records. Provide quality engineering guidance and support to New Product Introduction (NPI) projects, and as part of change management ensuring all quality deliverables are completed on time and in compliance with regulatory and internal requirements.

Work closely with the validation technical SME to ensure effective verification and validation (V V) of new products and processes within the NPI lifecycle. Champion thorough investigation of nonconformities using our eQMS Quality Event process, including product non-conformances, process deviations, and customer complaints. Drive effective Corrective and Preventive Actions (CAPA) through structured data driven root cause analysis (e.g., 5 Whys, Fishbone, FMEA).

Drive improvements in design, product, and process changes by ensuring changes are impact and risk assessed, documented and implemented in line with quality standards. Collaborate with cross-functional teams (Engineering, Manufacturing, Supply Chain, Quality) to implement quality improvements, in line with the WMFTS Quality Strategy. Support validation activities by ensuring the development and maintenance of validation protocols, procedures, and documentation in line with policy and process.

Be part of the internal audit team, conducting and generating audit reports to drive process improvements. Provide training, coaching and guidance on quality tools, systems, and best practices to colleagues and stakeholders. Promote a culture of quality, continuous improvement, and risk-based thinking throughout the product lifecycle and across all functions.

Other duties as assigned. Skills/Experience Bachelor’s degree in engineering, or a scientific discipline. Minimum of 5 years’ experience in Quality Assurance within a regulated industry.

Proven working knowledge of ISO 13485 and ISO 9001 standards. Strong ability to engage and communicate effectively with cross-functional stakeholders. Demonstrated expertise in product and process validation methodologies.

In-depth understanding of the design and development lifecycle. Proficient in conducting internal audits; lead auditor certification is highly desirable. Established track record in driving continuous improvement initiatives and applying lean methodologies.

Advanced problem-solving capabilities, including root cause analysis and effective CAPA (Corrective and Preventive Action) management. Excellent communication, planning, and organisational skills Resilient and delivery-focused, with a strong ability to manage change in dynamic environments

Free account
Stop reading job ads. Get the ones that fit.
One free account turns this page into a shortlist built around your stack, your level and your pay.
Match on every job. Stack, seniority, pay and location, scored against your profile.
2,073,754 open roles. Read straight off company career pages, refreshed every day.
Unlimited applications. Every one you send is tracked in one place, on-site or on a company board.
3 tailored CVs a month. Rewritten for the exact job you are applying to. Included free.
Create a free account Continue with Google
Free forever. No card. Under a minute.

Your match

How well do you fit this role?
Two answers are enough for a real match. No account needed.
Check my fit
Answers stay in this browser until you create an account.

Recommended for you based on this role

Industrial Engineering
Similar stack
Same company
Devens
In office · 3+ years exp · High School Diploma · Atlanta
Apply
$131k – $237k per year · In office · Secret · Full-Time · 12+ years exp · Bachelor's Degree · Huntsville
SpaceTech
FMEA
Cameo Systems Modeler
MedTech
Human Factors Engineering
Defense
MIL-STD-882
Apply
$108k – $195k per year · In office · Secret · Full-Time · 8+ years exp · Bachelor's Degree · Huntsville
SpaceTech
Cameo Systems Modeler
IBM DOORS
MBSE
MedTech
Verification & Validation
Apply
Mechanical Engineer 2 days ago
$87k – $157k per year · In office · Secret · Full-Time · 4+ years exp · Bachelor's Degree · Huntsville
Design
SolidWorks
AutoCAD
SpaceTech
CATIA
GD&T
Apply
$70k – $126k per year · Remote (United States) · Full-Time · 2+ years exp · Bachelor's Degree · United States
Apply
In office · Devens
MedTech
CAPA
Apply
Quality Engineer 1 day ago
In office · 2+ years exp · Bachelor's Degree · Devens
SpaceTech
FMEA
MedTech
ISO 13485
Verification & Validation
CAPA
Apply
$134k – $205k per year · In office · Full-Time · 7+ years exp · Bachelor's Degree · Devens
Chips/EDA
Statistical Process Control
Design
SolidWorks
AutoCAD
SpaceTech
FMEA
Apply
$135k – $163k per year · In office · Full-Time · 6+ years exp · Bachelor's Degree · Devens
Life Sciences
GMP
Apply
$93k – $112k per year · In office · Full-Time · 3+ years exp · Bachelor's Degree · Devens
Life Sciences
GMP
ICH Guidelines
MedTech
CAPA
Apply
See all jobs
This is one of many
2,073,754 more open roles from verified company boards, updated every day.