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Engineering - Project Manager

Job in Meriden, New Haven County, Connecticut, 06451, USA
Listing for: Akraya, Inc.
Contract position
Listed on 2026-07-10
Job specializations:
  • Engineering
    Manufacturing Engineer, Quality Engineering
  • Manufacturing / Production
    Manufacturing Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 135200 - 145600 USD Yearly USD 135200.00 145600.00 YEAR
Job Description & How to Apply Below
Position: Engineering - Project Manager : 26-01901

Primary Skills

  • Solid Works (advanced)
  • MS Office (advanced)
  • Technical Writing (advanced)
  • Project Management (advanced)
  • Risk Assessment (intermediate)
Contract Details
  • Contract Type: W2
  • Duration: 12 Months
  • Location:

    Meriden, CT - 06450 (Onsite)
  • Pay Range: $65 - $70 per hour on W2
Job Summary

This role is integral to enhancing manufacturing capabilities by overseeing the lifecycle of new and existing equipment. You will ensure all capital projects deliver high-quality, safe, and efficient production solutions. Your efforts will directly contribute to improving productivity, capacity, and overall operational effectiveness within the manufacturing sites.

Key Responsibilities
  • Spearhead the design, build, and installation of new manufacturing equipment.
  • Drive projects focused on enhancing productivity and cost reduction of existing machinery.
  • Manage vendor relationships to ensure successful equipment development and implementation.
  • Utilize engineering tools for process improvement and risk mitigation.
  • Ensure all project execution aligns with strict quality and safety protocols.
  • Proficient in technical writing including authoring engineering protocols, reports, and procedures.
  • Medical Device/Biopharmaceutical manufacturing experience desired (e.g., GMP, FDA, ISO 13485).
Must-Have Skills
  • Demonstrated experience managing capital equipment projects.
  • Proficiency in technical documentation and reporting.
  • Strong problem-solving and coordination abilities.
  • Experience in medical device or biopharmaceutical manufacturing, including familiarity with GMP and FDA regulations.
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