Pharmaceutical Process Engineer

Massachusetts-based life sciences client is currently in need of a Process Engineer to support their commercial manufacturing operations, process improvements, technical transfers, validation activities, and troubleshooting within a regulated production environment.

In this role, you will be a technical resource supporting manufacturing, quality, engineering, and supply chain teams while ensuring compliance with cGMP requirements and maintaining reliable production performance.

Ideally looking for at least five years of experience supporting medical device, pharmaceutical, sterile injectable, or radiopharmaceutical manufacturing environments. Experience leading deviation investigations, root cause analysis, CAPAs, process validation, equipment qualification, change control, and technical documentation is preferred.

You should have a solid understanding of cGMP regulations, aseptic processing, cleanroom operations, and quality systems, along with the ability to drive continuous improvement initiatives and support regulatory inspections.

At this time, only US citizens and permanent residents / greencard holders are being considered