Supplier Quality Engineer -Raynham

Corin Group; Raynham (MA); On-site; USD 87,000 - 102,000; Full time

Benefits offered by this job

Career development

Employee referral program

Collaborative culture

Job summary

Corin Group in Raynham, MA is seeking an experienced Supplier Quality Engineer to ensure supplier-delivered parts meet manufacturing specs, quality standards, and regulatory requirements. You will drive supplier quality improvements, investigate non-conformances, support new product introductions, and maintain robust QMS processes within a collaborative team.

Key responsibilities include leading supplier development, root cause analysis, CAPA initiation, and maintaining supplier performance

Qualifications

• Bachelors degree in Engineering, Science, or equivalent.
• 5+ years in Quality Engineering within mechanical/manufacturing environments.
• Experience in supplier quality management and supplier development.
• Strong root cause analysis and problem-solving skills.
• Experience managing non-conformances, CAPAs, and supplier corrective actions.

Responsibilities

• Collaborate with suppliers to implement defect prevention and continuous improvement.
• Lead supplier quality development activities to improve performance and capability.
• Analyze root cause data and implement effective CAPAs to minimise disruptions.
• Manage supplier non-conformances and maintain quality records in eQMS.
• Provide technical support to suppliers and manage customer-specific quality requirements.
• Ensure products meet quality standards while supporting cost reduction and customer satisfaction.

Skills

Root cause analysis

CAPA

Supplier quality management

Supplier development

Communication

Driving licence

Education

Bachelor's degree in Engineering or Science

Tools

eQMS

Job description

Supplier Quality Engineer – Raynham

We are seeking an experienced and proactive Supplier Quality Engineer to join our Quality team. In this role, you will be responsible for ensuring that products delivered by suppliers consistently meet manufacturing specifications, quality standards, and regulatory requirements.

Working closely with both internal teams and external suppliers, you will drive supplier quality improvement initiatives, investigate non-conformances, support new product introductions, and ensure robust quality management processes are maintained. This is an excellent opportunity for a quality-focused professional who thrives in a collaborative environment and enjoys solving complex manufacturing and supplier challenges.

What you’ll do

• Partner with suppliers to develop and implement best practices that focus on defect prevention, waste reduction, variation control, and continuous improvement.
• Lead supplier quality development activities to improve performance and capability.
• Collect and review root cause analyses, ensuring effective corrective actions are implemented to minimise production disruptions.
• Manage supplier non-conformances and quality records through the Electronic Quality Management System (eQMS).
• Provide technical support to suppliers and manage customer-specific quality requirements.
• Ensure supplied products consistently meet quality standards while supporting cost reduction and customer satisfaction objectives.
• Introduce and drive supplier improvement initiatives.
• Support new product introductions, ensuring quality robustness and supplier readiness.
• Work on complex projects and quality improvement programmes with a significant business impact.
• Collaborate with suppliers to ensure compliance with Safety, Quality, Cost, and Delivery requirements.
• Conduct regular supplier quality review meetings and provide reports to senior management.
• Develop, maintain, and report on supplier rating and performance management systems.
• Perform supplier audits and assessments to ensure ongoing compliance with business and regulatory requirements.
• Ensure adherence to Quality Management System (QMS) requirements, including ISO 13485, GMP, and FDA 21 CFR Part 820 standards.
• Support Corrective and Preventive Action (CAPA) activities, ensuring timelines and process requirements are achieved in line with company procedures.

About You

To be successful in this role, you will possess a strong quality engineering background and experience working within a regulated manufacturing environment.

• Degree in Engineering, Science, or an equivalent technical discipline.
• Minimum of 5 years' experience in a Quality Engineering position within a mechanical engineering or manufacturing environment.
• Experience in supplier quality management and supplier development.
• Strong root cause analysis and problem-solving skills.
• Experience managing non-conformances, CAPAs, and supplier corrective actions.
• Excellent communication and stakeholder management skills.
• Full US driving licence.
• Ability to conduct supplier audits and build effective working relationships with suppliers.

Desirable

• Experience within the Medical Device industry.
• Knowledge of ISO 13485, GMP, and FDA 21 CFR Part 820 regulations.
• Experience supporting new product introductions (NPI).
• Medical device technology and software experience.
• Lead Auditor qualification or supplier auditing experience.

What We Offer

• Opportunity to work within an innovative and highly regulated manufacturing environment.
• Exposure to global suppliers and cross-functional teams.
• Career development and progression opportunities.
• The base pay range for this position is $87,000-102,000. The specific pay offered may be influenced by a variety of factors, including the candidate’s experience, education, and skill set.
• A collaborative culture focused on quality, innovation, and continuous improvement.
• Employee referral program where you can earn incentives for each successful hire you recommend

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