AGC Biologics, Inc.
Facility/Utility Engineer -Senior/Principal
AGC Biologics, Inc. - Boulder, Colorado, United States, 80301
Work at AGC Biologics, Inc.
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Overview
Facility/Utility Engineer -Senior/Principal page is loaded Facility/Utility Engineer -Senior/Principal Apply locations Boulder, Colorado, USA Longmont, Colorado, USA time type Full time posted on Posted 10 Days Ago time left to apply End Date: October 13, 2025 (30+ days left to apply) job requisition id JR102269
Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe, creating a healthier and happier tomorrow. Our mission is to work side by side with our customers in order to improve patients’ lives by bringing new biopharmaceuticals to market. JOB SUMMARY Are you a problem-solver who thrives in technical environments? We are looking for a
Senior/Principal Utilities/Facilities Engineer
to bring expertise in designing, maintaining, and optimizing critical utility systems that support our biomanufacturing operations in
Boulder and Longmont, CO
. In this role, you’ll oversee systems like clean rooms, HVAC, boilers, chillers, CIP (Clean-in-Place) skids, compressed air, clean steam generation, RO, and WFI systems. You will play a key role in startup, commissioning, and lifecycle management while ensuring compliance with regulatory standards (FDA, EMA, OSHA). This is an excellent opportunity to make a real impact on production reliability, safety, and quality. Schedule
Full-time role based in Boulder, CO.
Monday-Friday
Principal Responsibilities
Act as the system owner for utility and facility equipment in assigned areas.
Serve as the liaison between QC, MSAT, capital projects, automation, and maintenance support teams.
Oversee CIP skid reliability, cycle development, and validation programs.
Manage HVAC design and cleanroom classifications to ensure low bioburden drug substance manufacturing.
Ensure all work complies with industry and regulatory standards (FDA, EMA, OSHA) and internal quality and safety guidelines.
Supervise the design, startup, and maintenance of utility systems across facilities.
Collaborate with mechanical, electrical, and automation engineering teams.
Lead root cause analysis (RCA) and resolution of major equipment breakdowns and quality issues.
Utilize CMMS systems (e.g., Blue Mountain) for equipment management.
Develop and implement utility system strategies and engineering standards to improve reliability.
Lead continuous improvement initiatives and plan for long-term equipment upgrades.
Own and close quality records such as change records, deviations, and CAPAs.
Deliver utility and expansion projects on time and within budget.
Promote and maintain a safe and compliant working environment.
Plan and analyze utility capacity, system obsolescence, and site master planning strategies.
Manage vendor contracts and relationships.
Perform other related duties as assigned.
Knowledge, Skills & Abilities
Flexible and adaptable to evolving business conditions.
Excellent written, verbal, and interpersonal communication skills.
Strong analytical and problem-solving abilities.
Proficiency in MS Office (Word, Excel, Outlook, PowerPoint).
Experience with CMMS software (e.g., Blue Mountain).
Ability to troubleshoot complex technical issues and recommend solutions.
Knowledge of utility system design, operation, and startup.
Familiarity with electrical, mechanical, and control systems.
In-depth understanding of cGMP documentation requirements.
Ability to read and interpret engineering drawings, P&IDs, and electrical schematics.
Experience with Lean principles, continuous improvement, and cost reduction initiatives.
Budget management experience.
Ability to maintain clear and accurate documentation.
Education & Experience
BS/MS in Engineering (Chemical, Biotechnology, Mechanical, or Electrical).
Senior level: Minimum of 8 years relevant experience (BS), 6 years (MS), or 5 years (PhD).
Principal level: Minimum of 10 years of relevant industry experience (BS), 8 years (MS), or 6 years (PhD).
Minimum of at least 3 years of troubleshooting automated systems in Biotech/Pharma processes.
Lean/Six Sigma certification is desirable.
Experience with upstream and downstream unit operations (e.g., centrifugation, filtration, chromatography, bioreactors) is preferred.
Project management experience with automation CAPEX projects is a plus.
Experience writing technical reports and using CMMS systems.
Compensation Range: Utilities/Facilities Engineer, Senior $108,080 - $148,610 Utilities/Facilities Engineer, Principal $142,960 - $196,570 Our culture at AGC Biologics is defined by the six core values: Knowledge, Trust, Quality, Ingenuity, Accountability and Teamwork. Our core values stem from our team members and are embedded into our DNA. They provide a common language and understanding of how we as an organization are connected across three continents. Our core values serve as a compass and reminder of how we achieve our purpose of bringing hope to life for patients around the globe. AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan. We currently employ more than 2,500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients’ most complex challenges, including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more, visit
www.agcbio.com.
W
ant to keep posted about our growth and learn more about our company? Follow us on LinkedIn and give us a quick Like on Facebook ! AGC Biologics offers a highly competitive compensation package and a friendly, collaborative culture that values personal initiative and professional achievement. AGC Biologics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances.
About AGC Biologics
AGC Biologics is a leading global biopharmaceutical Contract Developmentand Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan. We currently employ more than 2,500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients’ most complex challenges, including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more, visit
www.agcbio.com
.
#J-18808-Ljbffr
Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe, creating a healthier and happier tomorrow. Our mission is to work side by side with our customers in order to improve patients’ lives by bringing new biopharmaceuticals to market. JOB SUMMARY Are you a problem-solver who thrives in technical environments? We are looking for a
Senior/Principal Utilities/Facilities Engineer
to bring expertise in designing, maintaining, and optimizing critical utility systems that support our biomanufacturing operations in
Boulder and Longmont, CO
. In this role, you’ll oversee systems like clean rooms, HVAC, boilers, chillers, CIP (Clean-in-Place) skids, compressed air, clean steam generation, RO, and WFI systems. You will play a key role in startup, commissioning, and lifecycle management while ensuring compliance with regulatory standards (FDA, EMA, OSHA). This is an excellent opportunity to make a real impact on production reliability, safety, and quality. Schedule
Full-time role based in Boulder, CO.
Monday-Friday
Principal Responsibilities
Act as the system owner for utility and facility equipment in assigned areas.
Serve as the liaison between QC, MSAT, capital projects, automation, and maintenance support teams.
Oversee CIP skid reliability, cycle development, and validation programs.
Manage HVAC design and cleanroom classifications to ensure low bioburden drug substance manufacturing.
Ensure all work complies with industry and regulatory standards (FDA, EMA, OSHA) and internal quality and safety guidelines.
Supervise the design, startup, and maintenance of utility systems across facilities.
Collaborate with mechanical, electrical, and automation engineering teams.
Lead root cause analysis (RCA) and resolution of major equipment breakdowns and quality issues.
Utilize CMMS systems (e.g., Blue Mountain) for equipment management.
Develop and implement utility system strategies and engineering standards to improve reliability.
Lead continuous improvement initiatives and plan for long-term equipment upgrades.
Own and close quality records such as change records, deviations, and CAPAs.
Deliver utility and expansion projects on time and within budget.
Promote and maintain a safe and compliant working environment.
Plan and analyze utility capacity, system obsolescence, and site master planning strategies.
Manage vendor contracts and relationships.
Perform other related duties as assigned.
Knowledge, Skills & Abilities
Flexible and adaptable to evolving business conditions.
Excellent written, verbal, and interpersonal communication skills.
Strong analytical and problem-solving abilities.
Proficiency in MS Office (Word, Excel, Outlook, PowerPoint).
Experience with CMMS software (e.g., Blue Mountain).
Ability to troubleshoot complex technical issues and recommend solutions.
Knowledge of utility system design, operation, and startup.
Familiarity with electrical, mechanical, and control systems.
In-depth understanding of cGMP documentation requirements.
Ability to read and interpret engineering drawings, P&IDs, and electrical schematics.
Experience with Lean principles, continuous improvement, and cost reduction initiatives.
Budget management experience.
Ability to maintain clear and accurate documentation.
Education & Experience
BS/MS in Engineering (Chemical, Biotechnology, Mechanical, or Electrical).
Senior level: Minimum of 8 years relevant experience (BS), 6 years (MS), or 5 years (PhD).
Principal level: Minimum of 10 years of relevant industry experience (BS), 8 years (MS), or 6 years (PhD).
Minimum of at least 3 years of troubleshooting automated systems in Biotech/Pharma processes.
Lean/Six Sigma certification is desirable.
Experience with upstream and downstream unit operations (e.g., centrifugation, filtration, chromatography, bioreactors) is preferred.
Project management experience with automation CAPEX projects is a plus.
Experience writing technical reports and using CMMS systems.
Compensation Range: Utilities/Facilities Engineer, Senior $108,080 - $148,610 Utilities/Facilities Engineer, Principal $142,960 - $196,570 Our culture at AGC Biologics is defined by the six core values: Knowledge, Trust, Quality, Ingenuity, Accountability and Teamwork. Our core values stem from our team members and are embedded into our DNA. They provide a common language and understanding of how we as an organization are connected across three continents. Our core values serve as a compass and reminder of how we achieve our purpose of bringing hope to life for patients around the globe. AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan. We currently employ more than 2,500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients’ most complex challenges, including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more, visit
www.agcbio.com.
W
ant to keep posted about our growth and learn more about our company? Follow us on LinkedIn and give us a quick Like on Facebook ! AGC Biologics offers a highly competitive compensation package and a friendly, collaborative culture that values personal initiative and professional achievement. AGC Biologics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances.
About AGC Biologics
AGC Biologics is a leading global biopharmaceutical Contract Developmentand Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan. We currently employ more than 2,500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients’ most complex challenges, including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more, visit
www.agcbio.com
.
#J-18808-Ljbffr