HVAC Engineer


Danmark
Contract
Negotiable
Manufacturing
CR/598738_1783071853
HVAC Engineer

We are seeking an experienced HVAC Engineer to join a major pharmaceutical project in Copenhagen. The successful candidate will be responsible for supporting the design, installation, commissioning, qualification, and ongoing optimisation of HVAC systems within GMP-regulated manufacturing and laboratory facilities.

This position will play a key role in ensuring HVAC systems meet operational, quality, regulatory, and project requirements while maintaining compliance with pharmaceutical industry standards.

Key Responsibilities

  • Support the design, review, and implementation of HVAC systems for pharmaceutical and biotechnology facilities.
  • Oversee HVAC installation activities and ensure work is completed in accordance with project specifications and engineering standards.
  • Participate in commissioning, qualification, and validation activities, including IQ, OQ, and performance testing.
  • Ensure cleanroom and controlled environment requirements are achieved and maintained.
  • Review and approve technical documentation including drawings, specifications, protocols, and reports.
  • Collaborate with engineering, CQV, quality, manufacturing, and project management teams throughout the project lifecycle.
  • Troubleshoot HVAC-related issues and implement corrective and preventative actions.
  • Monitor contractor performance and provide technical guidance during project execution.
  • Ensure compliance with GMP, health and safety, and regulatory requirements.
  • Support project planning, scheduling, risk assessments, and change control activities.

Requirements

  • Bachelor's degree in Mechanical Engineering or a related engineering discipline.
  • Proven experience as an HVAC Engineer within the pharmaceutical, biotech, life sciences, or other highly regulated industries.
  • Strong knowledge of cleanroom HVAC systems, air handling units (AHUs), airflow management, pressure cascades, and environmental controls.
  • Experience supporting commissioning, qualification, and validation activities.
  • Understanding of GMP regulations and pharmaceutical facility requirements.
  • Ability to review and interpret P&IDs, HVAC schematics, technical drawings, and engineering documentation.
  • Strong communication and stakeholder management skills.
  • Fluent English language skills; Danish is advantageous but not essential.

Preferred Experience

  • Pharmaceutical manufacturing facilities.
  • Cleanrooms and classified environments.
  • USP/DSP facilities.
  • API, fill-finish, or aseptic production environments.
  • Large-scale capital expansion or brownfield projects.
  • Working within cross-functional engineering and project teams.

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