Process Engineer II

Brief Job Description

A career at Resilience is more than just a job – it’s an opportunity to change the future. Resilience is a technology-focused biomanufacturing company that’s changing the way medicine is made. We’re building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need. For more information, please visit

The Process Engineer II owns the technical process for assigned IDAP equipment, working with limited supervision to keep assigned processes capable, compliant, and improving. Drives continuous improvement, validation, and troubleshooting on assigned equipment, and authors the controlled documentation that supports it. Partners with Manufacturing, Quality, Maintenance, and equipment suppliers to resolve technical issues and deliver assigned projects on time.

Owns the technical process for assigned IDAP equipment; defines and maintains centerlines, critical process parameters, material fit for use, and operating procedures to ensure a capable, repeatable process. Drives continuous improvement for assigned IDAP processes, including changeover reduction, yield and OEE improvements, maintenance reliability, and waste reduction. Tracks equipment data, capabilities, utilization, efficiencies, and obsolescence for assigned assets; manages asset lifecycle and develops user requirements for new asset procurement.

Provides engineering and project management for assigned projects, including developing project justification, tracking milestones, and informing capital planning.

Leads validation activities for assigned processes, defining success criteria, confirming process capability, and maintaining validated state through change. Authors and reviews URS, FAT, SAT, commissioning, and IQ/OQ/PQ protocols and reports for assigned processes. Troubleshoots assigned IDAP processes, diagnosing and resolving equipment and process deviations, including on-call support as required. Works directly with equipment and material suppliers on assigned processes to resolve technical issues.

Identifies, develops, and manages implementation of change controls for assigned processes to improve performance and address root causes. Performs and maintains risk management activities for assigned new and existing processes and equipment. Initiates deviations and independently leads technical investigations and impact assessments for assigned processes. Authors and reviews controlled documents including SOPs, Batch Records, and Rework procedures for assigned processes. Supports regulatory inspections as the process owner for assigned IDAP equipment.

Identifies technical training requirements for Operations, Engineering, and Maintenance for assigned processes, and develops and delivers training materials.

Prior experience or exposure in a GMP or regulated manufacturing environment, with a demonstrated ability to follow controlled procedures and quality standards. Prior training or hands‑on experience in one or more IDAP‑relevant technologies, such as mechanics, hydraulics, pneumatics, vacuum systems, electronics, PLCs, HMI, computerized systems, vision systems, aseptic/controlled environments, packaging equipment, process or cleaning validation, or change control. Baseline proficiency in at least one of the following disciplines: automation/controls, aseptic/packaging equipment, process/materials, maintenance, or validation.

Ability to work with limited supervision, exercising independent judgment on assigned processes.

Bachelor’s degree in Engineering or related science, and 2+ years of experience in a GMP or regulated pharmaceutical manufacturing environment. Experience with project management and process‑improvement methodologies (Six Sigma, Lean). Expertise in at least one of the following disciplines: automation/controls, aseptic/packaging equipment, process/materials, maintenance, or validation.

Work may…