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Salary
$44k – $54k per year
Location
In office (Raynham)

Confirmed on the employer's own hiring board on Nov 4, 2026. First seen by Alion on Oct 16, 2026.

Overview
Company
Impact
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Corin is an orthopaedic medical device company headquartered in Cirencester, England, that designs and makes hip, knee, ankle and shoulder implants and robotic-assisted surgery platforms. Founded in 1985, it offers the Apollo robotic platform with ApolloKnee and ApolloHipX, the OMNIBotics system and OPS patient-specific planning, with operations in Europe, Australia and the US, where it has a site in Raynham, Massachusetts. It hires manufacturing, quality, supplier quality and metrology staff, warehouse and logistics associates, software and development engineers, robotics technicians, product managers and orthopaedic sales executives.

Quality Inspector

Location: Raynham MAEmployment Type: Full-time - onsite

Join Our Team

We are seeking a detail-oriented and quality-focused Quality Inspector to play a critical role in ensuring our products meet the highest standards of quality, safety, and regulatory compliance. This role is responsible for inspecting incoming materials, in-process components, and finished products, while supporting our Quality Management System and regulatory requirements.

If you have experience in manufacturing quality inspection, enjoy working with precision measurement equipment, and take pride in delivering excellence, we would love to hear from you.

The Role

As a Quality Inspector, you will be responsible for ensuring that all products received from suppliers and released from manufacturing comply with specifications, company standards, and applicable regulatory requirements.

You will work closely with Quality, Manufacturing, Supply Chain, and Engineering teams to identify and address quality concerns, support inspection activities, and maintain accurate quality documentation.

What you’ll do

Perform incoming, in-process, and final inspections of materials and products.

Review manufacturing documentation, engineering drawings, specifications, and acceptance criteria.

Complete and maintain inspection documentation, including:

Device History Records (DHRs)

Inspection records

Non-Conforming Material Reports (NCMRs)

Conduct or support First Article Inspections (FAI) for new products and supplier changes.

Utilize inspection and measurement equipment, including calipers, micrometers, height gauges, and other testing tools.

Accurately document inspection findings and maintain quality records in accordance with company procedures.

Identify, document, and escalate non-conforming materials, products, or processes.

Support compliance with quality system requirements, including ISO 13485, FDA Quality System Regulations, and internal procedures.

Assist with document control activities related to calibration records, CAPAs, NCMRs, and other quality documentation.

Conduct periodic inventory cycle counts within the Quality Inspection area.

Perform spot checks and audits of quality records to ensure accuracy and integrity.

Support special inspection requests, investigations, and rework projects as required.

Adhere to Quality Management System (QMS) requirements in line with ISO 13485 and Good Manufacturing Practice (GMP) standards.

About You

To be successful in this role, you will be highly organised, methodical, and committed to maintaining high quality standards. You will have excellent attention to detail and be comfortable working within a regulated manufacturing environment.

Essential Requirements

High school diploma or equivalent.

Experience in a manufacturing quality inspection role, ideally within a regulated industry.

Ability to read and interpret engineering drawings and technical specifications.

Knowledge of inspection methods, measurement techniques, and quality standards. Experience of inspection equipment such as calipers, micrometers, and gauges.

Strong documentation and record-keeping skills.

Good computer skills and experience using electronic quality systems.

Excellent attention to detail and problem-solving skills.

Strong verbal and written communication skills.

Preferred

Technical qualification or degree in Engineering, Manufacturing, Quality, or a related discipline.

Experience working within medical device, pharmaceutical, aerospace, or other highly regulated industries.

Knowledge of ISO 13485, FDA 21 CFR Part 820, GMP, CAPA, and non-conformance processes.

Why Join Us?

Opportunity to work in a highly regulated and quality-driven environment.

Be part of a collaborative team committed to continuous improvement.

Contribute directly to the quality and safety of products that make a difference.

Professional development and career growth opportunities.

The base pay range for this position is $22.60- $27.40 per hour. The specific pay offered may be influenced by a variety of factors, including the candidate’s experience, education, and skill set."

Employee referral program where you can earn incentives for each successful hire you recommend

If you are passionate about quality and thrive in a precision-focused manufacturing environment, we encourage you to apply today.

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