Facilities & Equipment Engineer in Rochester

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Job DescriptionFacilities & Equipment Engineer

Onsite in Rocester, MN (relo provided)

Company Profile: Growing Radiopharmaceutical CDMO focused on Cancer

What You Will Be Doing

• Ensure the safe, compliant, and efficient operation of facility systems in a regulated radiopharmaceutical environment.
• Responsible for maintaining HVAC, utilities, cleanrooms, and building automation systems (BAS/BMS), while supporting preventive maintenance, troubleshooting, and calibration management of all facility and analytical equipment while adhering to cGMP and regulatory requirements.
• Collaborate with cross-functional teams such as Manufacturing, Quality, EHS, and Quality Control, etc. to support daily operations, continuous improvement initiatives, and new equipment commissioning and qualification.
• Ensure safe, reliable, and compliant operation of facility systems, including HVAC, utilities, cleanrooms, and BAS/BMS.
• Perform and support preventive and corrective maintenance activities for applicable facility and analytical equipment items.
• Troubleshoot equipment and system issues, implementing timely and effective solutions.
• Collaborate with teams such as Manufacturing, Quality, EHS, and Quality Control, etc. to support operations and compliance.
• Participate in commissioning, qualification, and validation (CQV) of new equipment and systems.
• Maintain compliance with cGMP, FDA, and other regulatory requirements.
• Utilize CMMS and automated monitoring systems for work management and system oversight.
• Contribute to continuous improvement initiatives to optimize facility reliability, safety, and efficiency.
• Provide on-call or off-hours support as required.
  
  

What you will bring to the table:

• Bachelor’s degree in Mechanical, Electrical, Facilities Engineering, or related discipline.
• 3–7 years of facilities engineering experience in a regulated biotech, pharmaceutical / radiopharmaceutical, or life sciences environment required.
• Strong knowledge of cGMP, FDA, and regulatory standards required.
• Experience with BAS/BMS, CMMS, and alarm/monitoring systems .
• Strong problem-solving, organizational, and troubleshooting skills.
• Excellent communication and collaboration abilities across cross-functional teams.
• Ability to provide after-hours and on-call support as needed.
  
  

Please email Kiera@ScientificSearch.com to learn more about this great opportunity!

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