Senior Process Manufacturing Engineer

Position Summary

Support and optimize chemical manufacturing processes to improve safety, quality, efficiency, reliability, and cost. Partner with Operations, Quality, Maintenance, Safety, R&D, and Supply Chain teams to troubleshoot issues, implement process and capacity improvements, support new product introductions, and ensure regulatory compliance.

This is an onsite position and may require travel 5-10% of the time.

What You'll do as a Senior Process Manufacturing Engineer

Operational Support

• Provide operations department with technical support to meet manufacturing quality and quantity objectives.
• Provide general oversight and monitoring of process equipment - including project coordination for maintenance, upgrades, and repairs when needed.
• Investigate process deviations, equipment issues, and production constraints.
• Lead root cause analysis and implementation of corrective and preventive actions.
• Create/edit written documents, test plans and reports that demonstrate technical rationale for associated decisions (e.g. qualifications, risk assessments, and work instructions).
• Maintain Piping and instrumentation Diagrams "P&IDs" and drawings.

Continuous Improvement

• Lead initiatives to optimize safety, quality, delivery, and cost.
• Apply Lean and Six Sigma methodologies.
• Identify opportunities to reduce waste.
• Support process improvement efforts.

Capacity Improvement & Project Management

• Identify and propose capacity improvement opportunities.
• Lead or support capital improvement projects.
• Develop project scopes, budgets, schedules, and technical requirements.
• Coordinate planning, procuring, installation, commissioning, validation and startup activities associated with new equipment.

New Product Transfers

• Evaluate and provide input to product development teams to help ensure the successful introduction of a new product.
• Create and document new chemical manufacturing processes as needed.
• Train operations personnel on new processes.
• Work with cross-functional teams to drive back lessons learned as new products/processes are being developed.

The Experience, Skills and Abilities Needed

Required

• Bachelor's Degree in Engineering
• Minimum of 5 years of process engineering experience in manufacturing, chemical processing, or related. experience
• Experience managing engineering projects from the planning phase through validation.

Preferred

• Prefer BS in Chemical, Mechanical, or Industrial Engineering
• Strong understanding of chemistry
• Prefer experience within the medical device manufacturing industry, or similar regulated industry.
• Familiarity with ISO 13485, FDA Design Control, CAPA, SCAR, and audit procedures.
• Experience in structured problem solving and use of statistical tools.
• Training and experience in Lean and Six Sigma.

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Pay range for this opportunity is$99,875.00-$129,250.00.This position is eligible for bonus participation.

Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc.

STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits: STERIS Benefits

Open until position is filled.

STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare and life sciences products and services around the globe. For more information, visit

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STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.

The full affirmative action program, absent the data metrics required by * 60-741.44(k), shall be available to all employees and applicants for employment for inspection upon request. The program may be obtained at your location's HR Office during normal business hours.