Principal Process Engineering Lead Biopharma Equipment

Regeneron Pharmaceuticals; City of Troy (NY); Sur place; USD 88 000 - 169 000; Plein temps

Résumé du poste

Regeneron Pharmaceuticals in Troy, NY is seeking a Senior Project Engineer to join our Project Engineering team. You will design, specify, and commission process and clean utility equipment, lead deviation investigations, and provide engineering support across manufacturing processes.

The role involves managing mid-to-large projects, supervising contractors, and ensuring compliance with cGMP standards. Onsite work hours are Monday–Friday, with up to 10% travel.

Qualifications

• Bachelor's degree in Chemical Engineering or related field.
• 5+ years of project/process engineering experience for Senior Project Engineer.
• Direct experience with biopharmaceutical process equipment preferred.
• Strong understanding of process control systems and automation.
• Experience planning and tracking project activities and schedules.

Responsabilités

• Design and specify cGMP process equipment, piping, and controls, including engineering documentation.
• Manage mid-to-large projects for process equipment and clean utilities, including start-up, commissioning, and site acceptance.
• Lead design review and installation of equipment.
• Prepare piping and instrumentation diagrams and develop Process Flow Diagrams.
• Support QA/Validation with design documents and protocol execution.
• Investigate process equipment, utility, and control system anomalies, implementing corrective and preventive actions.
• Supervise mechanical, electrical, and automation contractors.

Connaissances

Process equipment design

Cross-functional collaboration

Project management

Communication skills

Formation

Bachelor's degree in Chemical Engineering

Description du poste

Regeneron Pharmaceuticals in Troy, NY is seeking a Senior Project Engineer to join our Project Engineering team. You will design, specify, and commission process and clean utility equipment, lead deviation investigations, and provide engineering support across manufacturing processes.

The role involves managing mid-to-large projects, supervising contractors, and ensuring compliance with cGMP standards. Onsite work hours are Monday–Friday, with up to 10% travel.