Process Engineer

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

• ◆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.

• ✓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.

The skills for success

Supply Chain Management, Business Partnership, Collaboration, Partnership building, Relationship management, Business accumen, Productivity management, Improve business processes, Advanced analytics, Data analytics, Manufacturing excellence.

What we offer

With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way.

We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy.