Quality Control Inspector II

Astrix Inc.

Shrewsbury (MA)

On-site

USD 48,000 - 55,000

Part time

14 days+

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Job summary

Astrix Inc. in Worcester County, MA is seeking a QA Inspector II to support ISO 9001 quality systems. You will inspect incoming materials, perform dimensional checks, and ensure conformance to specifications. Strong measurement skills and documentation experience are essential.

The contract runs 9 months with potential extension. Responsibilities include audits, deviations management, and continuous improvement within the QA program. Prior experience with medical devices is preferred.

Qualifications

  • Bachelor's degree or 5+ years quality inspection experience.
  • ISO 9001 or ISO 13485 quality management system experience.
  • Experience with medical devices or related inspection practices is preferred.

Responsibilities

  • Inspect incoming materials and approve/reject per procedures.
  • Verify and label parts according to documents.
  • Use calipers, Micro-Hite, and comparators for measurements.
  • Interpret drawings, specs, PO and SOW.
  • Perform dimensional inspections on machined parts.

Skills

Attention to detail
Communication
Quality mindset
Team collaboration

Education

Bachelor's degree in science
5+ years quality inspection experience

Tools

Calipers
Micro-Hite
Comparators
Microsoft Office

Job description

Pay Rate Low: 35 | Pay Rate High: 40

Our client is a leading life sciences company that develops and manufactures tools and materials used in the production of biologic drugs. They are looking for a skilled QA Inspector II to join their growing team in Worcester County, MA! This is a great opportunity to contribute to an innovative life science organization!

Pay rate: $35/hr. - $40/hr.

Location: Worcester County, MA

Job type: 9-month contract (possibility extension or hire)

Schedule: M-F 8a-5p

Job Summary The Contract Quality Control Inspector II reports to the Quality Inspector Lead, QA Manager, or Director and is responsible for supporting the ISO 9001 Quality Management System. The role focuses on inspecting, auditing, and documenting incoming materials and manufacturing processes using visual inspection methods and precision measuring equipment to ensure compliance with company and customer quality standards.

Responsibilities

  • Inspect incoming materials from suppliers and approve or reject them according to documented procedures.
  • Verify and apply part number labels to approved materials.
  • Use inspection tools such as calipers, Micro-Hite, and comparators.
  • Interpret engineering drawings, specifications, purchase orders, and statements of work.
  • Perform dimensional inspections on machined parts using precision measuring equipment.
  • Follow Safety Data Sheets (SDS) for proper chemical handling.
  • Apply sampling plans during inspections.
  • Report non-conforming materials to management and support root cause investigations.
  • Assist with corrective actions, deviations, complaints, and First Article Inspection (FAI).
  • Maintain accurate inspection records using Microsoft Office.
  • Identify continuous improvement opportunities within the quality program.
  • Support internal, supplier, and customer audits.
  • Review, investigate, and approve non-conforming material reports.
  • Comply with all safety regulations and company policies.

Qualifications

  • Bachelor's degree in a science‑related field or 5+ years of relevant quality inspection experience.
  • Minimum 3–5 years of experience working in an ISO 9001 or ISO 13485 Quality Management System.
  • Experience with medical devices, bioprocessing equipment, military, or aerospace inspection practices is preferred.
  • Proficient in Microsoft Office (Outlook, Excel, and Word).
  • Ability to use precision measuring equipment and inspect machined parts.
  • Strong understanding of engineering drawings and specifications.
  • Effective communication and collaboration skills across multiple departments.
  • Strong organizational skills with excellent attention to detail.
  • Knowledge of Good Documentation Practices (GDP) preferred.
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