In Process Final Inspector

Global Technical Talent; Marlborough; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading staffing agency is seeking an In Process Final Inspector to support medical device manufacturing operations in Marlborough. This role entails performing final and in-process inspections, reviewing Device History Records, and ensuring compliance with quality standards. Ideal candidates will have a strong knowledge of quality processes and a minimum of three years experience in a medical manufacturing environment. The position is onsite and full-time for a 5-month contract with competitive pay.

Benefits

Medical Insurance

Vision Insurance

Dental Insurance

401(k) Retirement Plan

Qualifications

• Strong knowledge of quality documentation and quality processes.
• High level of attention to detail and accuracy.
• Minimum 3 years of Quality Inspection experience in a medical manufacturing environment.

Responsibilities

• Perform final and in-process inspections to ensure product release.
• Review Device History Records for compliance.
• Collaborate with Engineering on documentation improvements.

Skills

Attention to detail

Quality documentation understanding

Reliability in regulated environments

Communication skills

Education

High school diploma or equivalent

Tools

Oracle

Agile

PLM systems

Job description

Primary Job Title

In Process Final Inspector

Alternate / Related Job Titles

• Quality Inspector – Medical Devices
• Final Inspection Technician
• QA Inspector – Medical Manufacturing
• Quality Assurance Technician

Location & Onsite Flexibility

Marlborough, MA — Onsite

Contract Details

• Position Type: Contract
• Contract Duration: 5 months
• Start: As Soon As Possible
• Pay Rate: $25/hour

Schedule

• Standard onsite schedule based on manufacturing operations
• Full-time hours during contract term

Position Summary

The In Process Final Inspector supports medical device manufacturing operations by performing final and in-process inspections, reviewing Device History Records (DHRs), and ensuring compliance with GMP, GDP, QMS, and ISO standards. This role plays a key part in product release, documentation accuracy, and continuous quality improvement within a regulated environment.

Key Responsibilities

• Perform detailed reviews of Device History Records (DHRs) to support final inspection and product release
• Review manufacturing records for replacement components, subassemblies, and in-process inspections
• Support documentation of Failure Investigation Reports and processing of Non-Conforming Materials in the PLM system, including identification and quarantine
• Conduct routine, field service, incoming, and special inspections to support validations and studies
• Reinforce Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) with manufacturing personnel
• Review and provide input on new Inspection and Test documentation
• Maintain QA tracking tools including QA Activity Collection Plans and First Pass Yield reports
• Collaborate with Engineering on documentation improvements and process changes
• Support incoming inspection, product returns, and calibration teams as needed
• Perform additional duties as assigned to meet operational and business needs

Compliance, Safety & Culture

• Comply with all company policies, SOPs, PPE requirements, QMSR, ISO standards, and safety regulations
• Demonstrate commitment to company values including integrity, collaboration, respect, and innovation
• Actively support a positive and inclusive work environment
• Participate in continuous improvement, lean initiatives, and sustainability practices
• Complete required training and workshops on time

Required Skills & Qualifications

Must-Have

• Strong knowledge of quality documentation and quality processes
• High level of attention to detail and accuracy
• Reliability and accountability in regulated environments
• Ability to work independently with minimal supervision

Required Technical & Functional Skills

• Working knowledge of GMP and GDP
• Familiarity with quality management systems (QMS) and medical device regulatory requirements
• Ability to interpret engineering drawings, specifications, and technical documentation
• Strong interpersonal and communication skills

Preferred

• Experience with Oracle and Agile
• Experience using PLM systems
• Proficiency with quality tools, metrics, and reporting systems

Teachable

• Computer systems and internal tools

Education & Experience

• Education: High school diploma or equivalent technical education preferred
• Experience:
  • Minimum 3–5 years of Quality Inspection experience in a medical manufacturing environment
  • Desired experience: 3 years
  • Underqualified threshold: 1 year
  • Overqualified threshold: 20 years

Physical & Safety Requirements

• Ability to sit, stand, walk, reach, and use hands/fingers for inspection tasks
• Ability to stoop, kneel, crouch, or crawl as required
• Lift, push, pull, and carry items up to 45 pounds
• Wear safety shoes compliant with site-specific PPE policies
• No routine exposure to blood, biohazards, or hazardous chemicals beyond standard manufacturing controls

Benefits

• Medical Insurance
• Vision Insurance
• Dental Insurance
• 401(k) Retirement Plan

About the Company

An innovative medical technology company dedicated to improving women’s health and well-being. The organization develops science-based solutions that enable earlier detection, diagnosis, and treatment of disease, driven by talented employees and a commitment to quality and innovation.

About GTT

GTT is a minority-owned staffing firm and a subsidiary of Chenega Corporation, a Native American-owned company based in Alaska. We value diverse and inclusive workplaces and partner with leading organizations across healthcare, life sciences, technology, and manufacturing throughout the U.S. and Canada.