Process Equipment Engineer

Position Overview

• The Process Equipment Engineer will provide technical oversight of process equipment, piping systems, and containment systems within a large-scale biopharmaceutical manufacturing facility. This owner-side, project-focused role requires close coordination with process engineering, construction, CQV, operations, and project delivery teams to ensure equipment and facility systems support process performance, maintainability, cleanability, safety, and operational readiness.

Key Responsibilities

• Provide technical oversight and support for process equipment, piping systems, and associated mechanical systems.
• Review equipment and system designs to ensure alignment with process requirements, operational needs, and facility standards.
• Evaluate equipment for maintainability, cleanability, reliability, operator safety, and containment requirements.
• Support mechanical integration activities throughout design, construction, installation, and startup phases.
• Partner with process engineering, CQV, construction, automation, and operations teams to resolve technical issues and support project execution.
• Participate in equipment design reviews, vendor coordination, field walkdowns, and system readiness assessments.
• Support commissioning, qualification, startup, and operational readiness activities for manufacturing systems.
• Identify and resolve equipment-related issues while helping maintain project schedules and startup objectives.

Required Qualifications

• Bachelor's degree in Mechanical Engineering, Chemical Engineering, Biochemical Engineering, or a related technical discipline.
• 5+ years of experience supporting process equipment and manufacturing systems within pharmaceutical, biotechnology, life sciences, chemical, or related industrial environments.
• Experience working with process equipment, piping systems, and mechanical utility systems.
• Understanding of GMP-regulated manufacturing facilities and equipment lifecycle requirements.
• Familiarity with process flow diagrams, P&IDs, equipment specifications, and vendor documentation.
• Experience supporting equipment installation, startup, commissioning, or qualification activities.
• Strong technical troubleshooting and problem-solving abilities.
• Ability to work effectively across multiple disciplines, including engineering, construction, operations, and quality.

Preferred Qualifications

• Experience supporting biologics, sterile manufacturing, API, peptide, or other pharmaceutical process systems.
• Experience on a greenfield pharmaceutical manufacturing project or large capital expansion program.
• Knowledge of containment systems and facility design considerations for highly potent compounds.
• Experience participating in FATs, SATs, commissioning, qualification, or startup activities.
• Familiarity with owner-side, EPCM, or large project delivery environments.
• Strong communication and stakeholder management skills.