Quality Engineer

Spirax-Sarco Engineering

• $85K — $105K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in engineering or a scientific discipline
  • 2-3 years of Quality Assurance experience in a regulated industry
  • Knowledge of ISO 13485 and ISO 9001 standards
  • Ability to communicate and engage effectively with cross-functional teams
  • Expertise in product and process validation methodologies
  • Understanding of the design and development lifecycle
  • Experience in conducting internal audits; lead auditor certification is desirable
  • Track record in continuous improvement initiatives and applying lean methodologies

Responsibilities

  • Develop and maintain quality management system (QMS) processes and documentation
  • Provide quality engineering support for New Product Introduction (NPI) projects
  • Partner with validation SME for effective product and process verification
  • Lead investigations of nonconformities using the eQMS process
  • Drive data-driven Corrective and Preventive Actions (CAPA)
  • Assess and document impacts of design and process changes to ensure quality compliance
  • Collaborate with cross-functional teams to implement quality improvements

Benefits

  • 5% employer 401K contribution and a 50% match on up to 3%
  • 16 weeks gender-neutral parental leave at 100% pay
  • Fertility assistance program covering services like IVF
  • Generous vacation and well-being days, plus numerous sick leave options
  • 3 paid volunteer days each year for community engagement
  • Various healthcare plans with HSA contributions and additional benefits
Full Job Description
Job Title: Quality Engineer
Location: WMFTS - USA - Supply - Devens, MA
Location Type: On-Site
Website: https://www.wmfts.com/en/
Group: https://www.spiraxgroup.com/

This role will focus on:

The Quality Engineer is responsible for support the development , and maintainenace of 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 a member of the site's subject matter expert (SME) team responsible for quality validation, risk management, and metrology, the 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:
  • 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 2-3 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 organizational skills
  • Resilient and delivery-focused, with a strong ability to manage change in dynamic environments


This position offers a salary range of (USD 85,000.00 - 105,000.00 Salaried). Final salary offers are determined by multiple factors, including education, experience, internal equity, geographic location, and the candidate's expertise, and therefore may vary from the range listed. For roles based outside Massachusetts, the applicable salary range may be lower.

At Watson-Marlow, we believe in taking care of our colleagues. We offer a generous benefits package, including:
  • Robust Retirement Plan: Benefit from a 5% employer 401K contribution, plus a 50% match on up to 3% of your contributions for added financial security, empowering your financial security.
  • Comprehensive and Supportive Parental Leave: Experience our inclusive, gender-neutral parental leave policy, offering 16 weeks at 100% pay. Upon your return, enjoy a gradual transition with a unique 80% work schedule while still receiving 100% of your pay for the first 6 months, ensuring a balanced reintegration into the workplace.
  • Fertility Assistant Program: Fertility Benefits to support you on your journey to building a family. It may include IVF, genetic testing, and other fertility-related services.
  • Generous Time Off: Enjoy ample time off to recharge and attend to life's circumstances with generous vacation and well-being day, 9 observed holidays, 1 floating holiday day, up to 15 caregiver days, and 80 hours of annual sick leave.
  • Community Engagement Opportunities: Make a difference with 3 paid volunteer days each year, encouraging you to give back to the community and causes you care about.
  • And Many More Benefits: Such as an offering of 3 healthcare plans with HSA contributions along with other benefits designed to support your well-being and professional growth. We invite you to explore all the ways we strive to create a fulfilling and rewarding work environment.

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