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Quality Engineer- Manufacturing

Worcester, MA

🔒 Direct submission to hiring team • Zero candidate fees

Role & Company Overview

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Employer
Azzur Group
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Location / Model
Worcester, MA
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Employment
Full-Time
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Recruitment Type
Direct to HR Pipeline
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Industry
General
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Company Size
🌐
Headquarters
United States
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Visa & Sponsorship
Global Talent Consideration
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Global Sponsorship Signal: This position is eligible for global talent consideration and work authorization sponsorship for top qualified international candidates.
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Human-Verified Opening: Inspected by Sarah Jenkins, CIPD • Hirely Editorial Team. Authenticated directly from Azzur Group's hiring pipeline • Zero recruiter markups or candidate fees. Verification Standards

📋 Role Overview & Responsibilities

From Discovery to Delivery™, Azzur Group provides the life science community full life-cycle solutions for all their GxP needs. From Azzur Cleanrooms on Demand™ facilities, to our labs, training centers and consulting offices across the nation, Azzur Group helps organizations start, scale, and sustain their growing enterprises. With nearly four decades of service to the life science community, we have become a trusted partner to the world's leading pharmaceutical, biotechnology, medical device, and healthcare companies, as well as their supply chain.

Responsibilities

  • Collaborate with manufacturing engineers to develop manufacturing processes, procedures, and production layouts tailored to assemblies, equipment installation, processing, machining, and material handling in medical device manufacturing.
  • Provide support in spearheading and conducting equipment validations, generating comprehensive reports that include IQ, OQ, PQ, and Test Method Validation.
  • Contribute to the innovation of manufacturing processes aligned with statistical process control, including the development of relevant techniques to enhance quality standards.
  • Offer expertise and guidance to engineering teams on design concepts and specification requirements to optimize equipment utilization and manufacturing techniques.
  • Lead the qualification process for new product supplied materials, ensuring that purchased products and components meet industry standards, regulatory requirements, and customer specifications through thorough qualification procedures.
  • Ensure rigorous adherence to regulatory and product quality compliance by overseeing processes and procedures within the manufacturing environment.
  • Assist in maintaining and revising documentation related to manufacturing operations, including work instructions, procedures, SOPs, P&ID flows, and associated change controls within the medical device manufacturing setting.

Requirements

Minimum 4 years experience Working knowledge of statistical data analysis

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Frequently Asked Questions

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Click the “Apply for this Position” button on this page to submit your application directly to Azzur Group without recruitment intermediary fees.

Is this position eligible for remote work or visa sponsorship? ▼

This position is located in Worcester, MA with potential relocation and sponsorship assistance depending on candidate qualifications.

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