Quality Control Inspector - 1820

SRG; Braintree (MA); On-site; USD 30,000 - 47,000; Full time

Job summary

Integra in Braintree, MA is seeking a Quality Control Inspector II for an on-site, 6‑month contract. You will inspect incoming, in‑process, and finished goods to ensure safety and quality in line with FDA, ISO 13485, and cGMP.

Collaborating with Manufacturing, Engineering, and Quality Assurance, you will document results, review data, support OOS investigations and CAPAs, and help prepare for audits. A high school diploma and basic lab skills are required; an associate degree or technical

Qualifications

• High school diploma or equivalent, working knowledge of lab and inspection practices.
• Familiarity with FDA and ISO standards in regulated manufacturing.
• Working knowledge of GMP and GDP.
• Moderate computer proficiency including Microsoft Office and databases.
• Strong attention to detail and ability to follow instructions precisely.

Responsibilities

• Perform in-process and final inspections using calipers, rulers, and dataloggers.
• Test materials and finished products for dimensions, performance, appearance, and assembly.
• Pull random samples at incoming, in-process, and final stages per procedures.
• Review inspection data for accuracy and help trend results.
• Support OOS investigations, nonconformances, and CAPAs with data.
• Maintain GDP and support document control and change control.
• Help prepare for FDA and customer audits and inspections.
• Keep inspection equipment, inventory, and workspace organized and compliant.
• Gown and enter the cleanroom when required.
• Suggest workflow improvements to inspection processes.

Skills

Lab practices and safety

FDA/ISO familiarity

GMP/GDP knowledge

MS Office/databases

Attention to detail

Follow instructions precisely

Education

High school diploma or equivalent

Associate degree or technical certification in life sciences or quality

Job description

[Integra] | [Braintree, MA] | [On-site] | [6 month contract to start]

About the Role

Quality Control Inspector II

Help make sure the products we ship are safe, reliable, and built to the highest standard. As a Quality Control Inspector II, you'll inspect and test incoming materials, in-process materials, and finished goods, keeping our quality records accurate and our operations in line with FDA regulations, ISO 13485, and cGMP requirements.

You'll work closely with Manufacturing, Engineering, and Quality Assurance, and you'll be a go-to resource for quality questions on the floor.

What You’ll Do

• Perform in-process and final inspections using tools like calipers, rulers, and dataloggers
• Test raw materials, intermediates, and finished products for dimensions, performance, appearance, and correct assembly
• Pull random samples at incoming, in-process, and final stages per sampling procedures
• Review inspection data for accuracy, help trend results, and escape excursions promptly
• Support OOS investigations, nonconformances, and CAPAs with factual data and documentation
• Contribute to test method validation and help write and update procedures, protocols, logbooks, and checklists
• Maintain Good Documentation Practices (GDP) and support document control, change control, and complaint handling
• Help prepare for FDA audits, customer audits, and regulatory inspections
• Keep inspection equipment, inventory, and your workspace organized and compliant
• Gown and enter the cleanroom as needed
• Suggest ideas to improve workflows and inspection processes

What You Bring

Required

• High school diploma or equivalent
• Working knowledge of standard laboratory and inspection practices and safety
• Familiarity with FDA and/or ISO standards in a regulated manufacturing environment
• Working knowledge of GMP and GDP
• Moderate computer proficiency, including Microsoft Office and database systems
• Strong attention to detail, with the ability to follow instructions precisely, recognize deviations, and recommend corrective action

Preferred

• Associate degree or technical certification in life sciences, quality, or a related field

Impellam Group and its brands are equal-opportunity employers committed to diversity and inclusion. All qualified applicants will receive consideration without regard to race, color, religion, gender, sexual orientation, pregnancy or maternity, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application, interview process, pre‑employment activity, and the performance of crucial job functions.

If you require additional disability considerations, modifications, or adjustments please let us know by contacting [e-mail] or fill out this form to request accommodations.