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Reliability Engineer- Biotechnology

Boston, MA

🔒 Direct submission to hiring team • Zero candidate fees

Role & Company Overview

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Employer
Thrive
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Location / Model
Boston, 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 Thrive's hiring pipeline • Zero recruiter markups or candidate fees. Verification Standards

📋 Role Overview & Responsibilities

A biotechnology client in Boston, MA is looking for a Facilities/ Reliability Engineer

Summary

The facilities site engineer reporting to global engineering and capital project management will be responsible for providing engineering expertise in a multi-site GMP manufacturing facility environment including in-depth knowledge of building mechanical, electrical and piping systems with their controls. Primary duties will include collaboration with multiple stakeholders to support robust operations of facility and equipment reducing unplanned downtime. The role includes engineering design, project management and change control management for facility related projects including manufacturing equipment, clean room, laboratory, and manufacturing suite renovations.

Responsibilities

Position Qualifications

Executes change management for equipment and other support systems including commissioning and/or implementation of other related initiatives as assigned

  • Implement science centric strategic decisions for capital projects and Validation based on the scientific knowledge, education and experience• Participate in design reviews for various capital projects and equipment with cost, efficiency and compliance always in mind• Creation and revision of commissioning protocols, reports, and engineering documents including, but not limited to, CQV, drawings, user requirement specifications and SOP’s.

Requirements

B.S. in Engineering discipline with 5-10+ years of relevant experience• Understanding and application of technical principles, theories, and concepts in the field, GMP, ISO, GAMP, ANSI.• Knowledge of facility related engineering disciplines (MEP) in GMP manufacturing environment

Frequently Asked Questions

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

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

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