Process Engineer

1 day ago


St Louis MO USA, United States STERIS Full time
Job Title: Process Engineer

STERIS is seeking a highly skilled Process Engineer to join our team in St. Louis, MO. As a Process Engineer, you will be responsible for establishing manufacturing process capability for new and reformulated products, supporting the execution of equipment qualification, cleaning, and process validation programs, and preparing and revising batch records, operating instructions, and cleaning instructions.

Key Responsibilities:
  • Support the execution of protocols to comply with FDA and cGMP requirements for equipment qualification, cleaning, and process validations.
  • Develop and implement lean culture and principles to improve manufacturing processes.
  • Develop plans, design of experiments, and schedules for establishing manufacturing process capability and introduction of new and reformulated products.
  • Interface with Product Development and Production to bring processes from research laboratory to full-scale manufacturing.
  • Research and test new technologies or processes to support new and existing product manufacture.
  • Support Project Engineering to obtain approval for Capital Appropriation Requests, design specifications, and equipment installation.
  • Provide personnel training, development of manufacturing instructions, and start-up of new processes and equipment.
  • Conduct process studies, identify opportunities for improvement, and support implementation of findings to optimize liquid blending systems.
  • Resolve specific manufacturing deficiencies through troubleshooting and implementation of corrective actions.
  • Develop and submit written reports, including objective, experimental, compilation of data, engineering analysis, conclusions, and recommendations.
Requirements:
  • Bachelor's degree in Engineering.
  • One to five years' experience in process engineering, production support, and/or batch chemical processing.
  • Project leadership skills, technical skills, and organizational skills required.
  • Familiarity with current Good Manufacturing Practices (cGMPs) and familiarity with FDA regulations preferred.
  • Good communications and interpersonal skills needed.
  • Experience in basic unit operations required.

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, life sciences, and dental products and services. STERIS is a $5 billion, publicly traded company with approximately 17,000 associates and customers in more than 100 countries.

If you need assistance completing the application process, please call the contact information provided. STERIS is an Equal Opportunity Employer and is committed to equal employment opportunity and the use of affirmative action programs 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, sexual orientation, gender identity, genetic information, and any other category protected by federal, state, or local law.


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