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Process Engineer – Biopharma Automation & Equipment Validation

Job in Providence, Providence County, Rhode Island, 02912, USA
Listing for: JMD Technologies Inc.
Full Time position
Listed on 2026-07-08
Job specializations:
  • Engineering
    Validation Engineer, Pharma Engineer, Quality Engineering, Process Engineer
  • Manufacturing / Production
    Validation Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Title: Process Engineer – Biopharma Automation & Equipment Validation

Location: Providence, RI (Onsite 5 days/week)

Employment Type: Contract

Status: Accepting Candidates

About the Role

Join a high-impact engineering team supporting the automation and optimization of manufacturing systems for advanced biopharmaceutical production. This role focuses on process equipment
, automation
, validation
, and technology transfer within a cGMP-regulated manufacturing environment.

Key Responsibilities
  • Lead process equipment development, specification, commissioning, qualification, and lifecycle support.
  • Drive equipment validation
    , FAT/SAT
    , risk assessments
    , and technology transfer activities.
  • Troubleshoot manufacturing equipment and implement process improvements to enhance reliability and efficiency.
  • Author and review URS
    , protocols, reports, SOPs, and engineering documentation.
  • Support deviations
    , CAPA
    , change control
    , and root cause investigations.
  • Collaborate with Manufacturing
    , Quality
    , Validation
    , MSAT
    , Facilities
    , and external vendors.
Qualifications
  • BS/MS in Engineering or a related technical discipline.
  • 5–7+ years of Process Engineering
    , Equipment Engineering
    , or Manufacturing Systems experience in a cGMP environment.
  • Hands‑on experience with equipment commissioning
    , qualification
    , validation
    , FAT/SAT
    , and URS development.
  • Strong knowledge of cGMP
    , 21 CFR Part 210/211
    , FMEA
    , CAPA
    , and Change Control
    .
  • Experience supporting biopharmaceutical
    , cell & gene therapy
    , or related GMP manufacturing processes.
  • Proven experience working with cross‑functional teams and equipment vendors.
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