Process Engineer

The Process Engineer will be responsible for establishing manufacturing process capability for new/reformulated/sustained products and supporting the execution of equipment qualification, cleaning, and process validation programs. This position will prepare and revise batch records, operating instructions, and cleaning instructions and conduct process improvement studies in the areas of operational productivity, process control, quality processing, employee safety, process yield improvement, and environmental impact in a lean environment. This position will also test new technologies, processes, controls or prototype equipment and support implementation as appropriate to optimize liquid blending systems while providing indirect supervision of technicians, interns and operators as required.

• Maintain a safe working environment by fully implementing the World Class safety initiatives and culture of STERIS Corporation and enforcing these initiatives at all times.
• Responsible for research and testing of new technologies or processes appropriate for support of new/existing product manufacturing. Complex process creation and maintenance (laser welding, etching).
• Provide personnel training, development of manufacturing instructions and start-up of new processes/equipment. IQ/OQ/PQ support.
• Responsible for conducting process studies, identifying opportunities for improvement and supporting implementation of findings to optimize manufacturing processes.
• Collaborate with Operations and CI to identify needs and opportunities for improvement.
• Collaborate with quality for specific manufacturing processes through troubleshooting and implementation of corrective actions.
• Monitor and provide solutions in terms of quality, yields, throughput, cycle times, process parameters, compliance, and safety and environmental requirements.
• Kaizen and lean events. SWI creation, revision and validation. OPS projects that deal with process and fixtures creation, modification and improvements. Tools and fixtures documentation and modification.
• V&V process standardization (V&V transfer & test procedure standardization).

• Bachelor's degree in Mechanical Engineering (BS) from an accredited four-year college or university; and 2-5 years of experience in process/industrial engineering, production support and/or design transfer.
• Project leadership skills, Lean/CI technical skills and organizational skills required
• Familiarity with QMS, and familiarity with FDA (ISO 13485)/local regulations
• 3D CAD and mechanical drafting (SolidWorks).
• Value stream & Process mapping.

Specific Work Preferences

• Solid Technical writing
• Fixture and tooling design
• Working within a manufacturing environment
• Understanding of design for assembly.

At STERIS, we invest in our employees and their families for the long term! STERIS wouldn't be where it is today without our incredible people. We shares our success together with you by rewarding you for your hard work and achievements.

Here is just a brief overview of what we offer:

• Competitive Pay
• Extensive Paid Time Off and (9) added Holidays.
• Excellent healthcare, dental, and vision benefits
• 401(k) with a company match
• Long/Short term disability coverage
• Parental Leave
• Additional add-on benefits/discounts for programs such as Pet Insurance
• Continued training and educations programs
• Excellent opportunities for advancement in a stable long-term career
• #LI-KS1 #LI-Onsite