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Engineering - Project Manager

Job in Meriden, New Haven County, Connecticut, 06450, USA
Listing for: Akraya
Contract position
Listed on 2026-07-09
Job specializations:
  • Engineering
    Manufacturing Engineer, Quality Engineering
  • Manufacturing / Production
    Manufacturing Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 65 - 70 USD Hourly USD 65.00 70.00 HOUR
Job Description & How to Apply Below
Position: Engineering - Project Manager : 26-01901

Manufacturing Equipment Project Manager

Primary

Skills:

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

Location:

Meriden, CT - 06450 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 (i.e. GMP, FDA, ISO 13485) experience desired

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, is highly preferred.

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