Senior Pharmaceutical HVAC & Cleanroom Engineer

Jedson Engineering

Cincinnati (OH)

On-site

USD 110,000 - 155,000

Full time

14 days+

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Job summary

Jedson Engineering is seeking a Registered Professional Mechanical Engineer with strong HVAC design experience for pharmaceutical process facilities. The role leads and supports HVAC and mechanical system design for regulated facilities, including cleanrooms and laboratories, ensuring cGMP compliance and contamination control.

You will coordinate across process, automation, validation and manufacturing teams, and support commissioning, qualification and regulatory reviews throughout concept to

Qualifications

  • Bachelor degree in Mechanical Engineering.
  • Active Professional Engineer (PE) license.
  • 10+ years of mechanical engineering experience in pharmaceutical, biotech, or life sciences facilities.

Responsibilities

  • Design and oversee HVAC systems supporting pharmaceutical manufacturing, laboratories, cleanrooms and process suites.
  • Coordinate with process engineering, validation, quality assurance, automation and manufacturing teams.
  • Lead or support commissioning, qualification, and validation activities.
  • Review contractor submittals, drawings, and engineering calculations.
  • Provide technical leadership for energy efficiency and reliability improvements.
  • Support audits, inspections, and regulatory reviews.

Skills

Pharmaceutical HVAC systems
Cleanroom Design
Aseptic manufacturing support
Energy efficiency

Education

Bachelor degree in Mechanical Engineering
PE license

Job description

Jedson Engineering is seeking a Registered Professional Mechanical Engineer with strong HVAC design experience for pharmaceutical process facilities. The role leads and supports HVAC and mechanical system design for regulated facilities, including cleanrooms and laboratories, ensuring cGMP compliance and contamination control.

You will coordinate across process, automation, validation and manufacturing teams, and support commissioning, qualification and regulatory reviews throughout concept to

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