Process Engineer - Biopharma Automation & Equipment Validation
JMD Technologies Inc.
Title: Process Engineer – Biopharma Automation & Equipment Validation Location: Providence, RI (Onsite 5 days/week) Employment Type: Contract Status: Accepting Candidates About the Role Join a high-impact engineering team supporting the automation and optimization of manufacturing systems for advanced biopharmaceutical production. This role focuses on process equipment , automation , validation , and technology transfer within a cGMP-regulated manufacturing environment. Key Responsibilities Lead process equipment development, specification, commissioning, qualification, and lifecycle support. Drive equipment validation , FAT/SAT , risk assessments , and technology transfer activities. Troubleshoot manufacturing equipment and implement process improvements to enhance reliability and efficiency. Author and review URS , protocols, reports, SOPs, and engineering documentation. Support deviations , CAPA , change control , and root cause investigations. Collaborate with Manufacturing , Quality , Validation , MSAT , Facilities , and external vendors. Qualifications BS/MS in Engineering or a related technical discipline. 5–7+ years of Process Engineering , Equipment Engineering , or Manufacturing Systems experience in a cGMP environment. Hands‑on experience with equipment commissioning , qualification , validation , FAT/SAT , and URS development. Strong knowledge of cGMP , 21 CFR Part 210/211 , FMEA , CAPA , and Change Control . Experience supporting biopharmaceutical , cell & gene therapy , or related GMP manufacturing processes. Proven experience working with cross‑functional teams and equipment vendors. #J-18808-Ljbffr JMD Technologies Inc.
Vacancy posted 1 day ago
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