Process Engineer

Reckitt · $88,000–$132,000 (stated in the posting)

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The Process Engineer supports oral solid dosage and liquid manufacturing operations by providing hands-on technical expertise, troubleshooting equipment and process issues, and driving continuous improvement initiatives. This role partners with Manufacturing, Quality, Validation, and Engineering teams to support daily production, process scale-up, equipment qualification, and validation activities while ensuring compliance with cGMP and regulatory requirements.

The successful candidate will lead technology transfer projects, support new product and equipment implementation, investigate deviations and batch failures, execute validation protocols (IQ/OQ/PQ and PPQ), and optimize manufacturing processes from pilot through commercial scale. This position is critical to supporting both existing operations and future facility expansions while improving product quality, reliability, and operational efficiency.

Your responsibilities

Provide technical support for day-to-day OSD, liquid, and semi-solid manufacturing operations, ensuring safe, compliant, and efficient production.

Lead troubleshooting, root cause investigations, and CAPA implementation for equipment issues, process deviations, batch failures, and yield improvements.

Manage technology transfer, process scale-up, and new product introductions from pilot development through commercial manufacturing.

Develop and execute validation activities, including equipment qualification (IQ/OQ/PQ), PPQ, and process revalidation, while partnering with cross-functional teams to qualify new equipment.

Drive continuous improvement initiatives through process optimization, technical documentation, engineering reviews, and adherence to cGMP and regulatory requirements.

This role is not currently sponsoring visas or considering international movement at this time.

The experience we're looking for

Bachelor's degree in Chemical Engineering, Pharmaceutical Sciences, or a related technical discipline, with 4-6 years of engineering experience in a pharmaceutical, biopharmaceutical, nutraceutical, or other regulated manufacturing environment.

Hands-on experience supporting technology transfer, process scale-up, validation, and commercial manufacturing operations within cGMP-regulated facilities.

Strong expertise in oral solid dosage (OSD) manufacturing processes and equipment, with working knowledge of liquid and semi-solid manufacturing operations and associated processing systems.

Demonstrated experience with equipment qualification (IQ/OQ/PQ), process validation, FDA/cGMP compliance, deviation investigations, root cause analysis (RCA), and CAPA implementation.

Proven ability to optimize manufacturing processes, develop technical documentation, and drive continuous improvement initiatives using Lean Manufacturing or similar methodologies.

USD $88,000.00 -  $132,000.00

Hiring range up to 110K

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