HVAC Engineer, Utility at AGC Biologics
Copenhagen, Capital Region of Denmark, Denmark -
Full Time


Start Date

Immediate

Expiry Date

22 Mar, 26

Salary

0.0

Posted On

22 Dec, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

HVAC Systems, GMP Compliance, Risk Management, Root Cause Analysis, Technical Documentation, Problem Solving, Troubleshooting, Project Support, Audit Representation, Collaboration, Continuous Improvement, Cleanroom Standards, Engineering Degree, Utility Management, Regulatory Knowledge, Operational Input

Industry

Pharmaceutical Manufacturing

Description
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. Have you already worked with HVAC systems in GMP environments and want full ownership rather than supervision? AGC Biologics is expanding its Utility team in Søborg and is looking for an experienced HVAC Engineer. This role is for someone who already understands regulated HVAC operations and is comfortable taking responsibility for systems that directly support GMP production. At our Søborg site, utilities are critical to product quality and patient safety. You will be part of the team that keeps our cleanrooms, labs, and production areas compliant, stable, and audit-ready. The Role As HVAC Engineer, you will own HVAC systems serving GMP-classified areas across the site. This is a hands-on, operational role with strong focus on compliance, risk reduction, and continuous improvement. You will work closely with production, QA, validation, maintenance, and project teams. This role is not entry-level. You are expected to already know how HVAC systems behave in regulated environments and how to work within GMP frameworks. Work Schedule & Flexibility Our facilities operate around the clock to support GMP production. Most work is carried out during regular business hours, but occasional evening or weekend work may be required to ensure uninterrupted operations. The HVAC Engineer Role As HVAC Engineer, you will take ownership of our GMP-critical HVAC systems together with two skilled technicians. While the technicians execute scheduled and unscheduled maintenance, your role will focus on: Ensuring stable, compliant, and efficient operation of HVAC systems across production, labs, and warehouses. Maintaining and improving technical documentation (SOPs, P&IDs, maintenance plans) in line with GMP standards. Driving risk management, root cause analysis, and implementation of corrective and preventive actions. Supporting CAPEX and OPEX projects with operational input to ensure smooth handover to operations. Representing utilities during audits and inspections with resilient, fact-based responses. Acting as the go-to HVAC specialist for stakeholders across the site. Focus & Development Path Initially, your primary responsibility will be HVAC. As you build capabilities and experience, your role will expand to include black and clean utilities, enabling you to contribute across the entire Utility team. What We Expect From You Proven experience working with HVAC systems in GMP-regulated pharmaceutical or biotech environments. Strong understanding of GxP and GMP requirements related to cleanroom HVAC. An engineering degree (mechanical, electrical, or similar) or equivalent technical background combined with relevant experience. Ability to independently troubleshoot issues and apply structured problem-solving methods such as A3, 5 Whys, or fishbone analysis. Comfortable working with documentation, deviations, and inspections. You should be confident operating in a regulated production environment with limited supervision. Nice to Have's Experience supporting the transition from project phase to operational ownership. Direct involvement in regulatory audits and authority inspections. Experience working in utility or facility teams in GMP production sites. Application To apply, submit your CV. We value depth of experience over meeting every box perfectly! The hiring process for this role begins week 2, 2026. 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. Want 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. AGC Biologics is a global CDMO headquartered in Seattle, Washington, USA. The company provides pharmaceutical development and manufacturing services for protein-based biologics, cell and gene therapies, messenger RNA. With locations across three continents, we specialize in the following modalities and substances: mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells. Our services range from process development, analytical development, cGMP manufacturing, quality control and quality assurance, and process validation.

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Responsibilities
The HVAC Engineer will own HVAC systems serving GMP-classified areas, ensuring stable and compliant operations. They will also maintain technical documentation and drive risk management initiatives.
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