Pharma HVAC Project Engineer: GMP & Validation Lead

DPS Group Global; Puurs; On-site; EUR 55,000 - 85,000; Full time

Job summary

DPS Group Global seeks a Project Engineer HVAC to lead end-to-end implementation and project management of HVAC and clean utilities projects in a pharmaceutical manufacturing environment, including cleanroom construction. The role covers conceptual, basic, and detailed engineering to align designs with internal standards and customer needs.

Responsibilities include coordinating purchase, installation, startup, and validation efforts; generating P&IDs and specifications; and ensuring GMP/ISO

Qualifications

• Higher technical education such as an Industrial or Civil Engineer degree.
• Experience with HVAC systems in a similar position is essential.
• Strong communication and interpersonal skills; ability to set priorities.
• Capable of working independently and in a team.
• GMP, ISO, ICH knowledge; risk management tools like FMEA.
• Proficiency in Dutch and English.
• Experience with Engineering (Capex) projects and MS Project is valued.

Responsibilities

• Coordinating purchase, installation, start-up, and verification/validation of equipment and piping.
• Generating P&IDs, functional specifications, and validation documents.
• Ensuring safety, quality, and regulatory compliance (GMP, ISO, ICH, Quality Standards).
• Facilitating Quality Risk Assessments.

Skills

Communication

Interpersonal skills

Prioritization

Team collaboration

Multitasking

Independent work

Assertiveness

Project coordination

Education

Engineering degree (Industrial/Civil)

Job description

DPS Group Global seeks a Project Engineer HVAC to lead end-to-end implementation and project management of HVAC and clean utilities projects in a pharmaceutical manufacturing environment, including cleanroom construction. The role covers conceptual, basic, and detailed engineering to align designs with internal standards and customer needs.

Responsibilities include coordinating purchase, installation, startup, and validation efforts; generating P&IDs and specifications; and ensuring GMP/ISO