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    Senior Process Engineer - St Louis, United States - STERIS

    STERIS
    STERIS St Louis, United States

    1 week ago

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    Description


    At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe.

    The Role Responsible for establishing manufacturing process capability for new/reformulated products. Execute equipment qualification, cleaning, and process validation programs.

    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.

    Test new technologies, processes, controls or prototype equipment and support implementation as appropriate to optimize liquid blending systems. Provide indirect supervision of technicians, interns and operators as required.

    What You Will Do Maintains a safe working environment by fully implementing the World Class safety initiatives and culture of STERIS Corporation and enforcing these initiatives at all times.

    Interact with all appropriate departments to facilitate the introduction of new manufacturing processes or changes to existing manufacturing processes. Executes protocols to comply with FDA and ISO requirements for equipment qualification, cleaning, and process validations. Develops protocols, resource requirements and timetables associated with the respective validation requirements. Develops plans and schedules for establishing manufacturing process capability of new/ reformulated products.

    Interfaces with Product Development and Production to bring these processes from the research laboratory through scale-up into full scale manufacturing.

    Responsible for research and testing of new technologies or processes appropriate for support of new/existing product manufacture. Works with Project Engineering to obtain approval for Capital Appropriation Requests, design specifications and equipment installation. Provides support in personnel training, development of manufacturing instructions and start-up of new processes/equipment. Resolves specific manufacturing deficiencies through troubleshooting and implementation of corrective actions. Responsible for development of lean culture and institution of lean principles. Develops and submits written reports including, objective, experimental, compilation of data, engineering analysis, conclusions and recommendations. Capable of developing new processes using instrumentation and PLCs to monitor and control engineering systems and equipment. Ensure compliance with the Quality System and Design Control requirements.

    Lead Design of Experiments work and process mapping and modeling(Aspen or similar).What You Will Need to be Successful Bachelor's degree in engineering or chemical engineering.

    Minimum of 5 or more years of experience in process engineering, production support and/or batch chemical processing. Ability to travel 15%-20% depending on the project.
    Preferred Experience Masters/PHD, preferred. 3 or more years of experience in pilot scale up, preferred. Familiarity with current Good Manufacturing Practices (cGMPs) FDA regulations, and Lean Manufacturing is preferred. Experience with cleanroom systems, preferred. Understanding of packaging materials and equipment including filling, closing, secondary and final packaging, preferred. Applied experience with flow calculations and energy balancing, preferred. Project Management experience, a plus. Agile experience, preferred. Experience working with non
    • Newtonian fluids, strongly preferred.
    Experience with scaling processes from lab to production, preferred. Skills Project leadership skills, technical skills and organizational skills required. Must have good communications and interpersonal skills.
    What STERIS Will Offer YouThe opportunity to join a company that will invest in you for the long-term. STERIS couldn't be where it is today without our incredible people. That's why we share in our success together by rewarding you for your hard work. Hiring people who are in it for the long run with STERIS is our ultimate goal.

    We do this by providing competitive salaries, healthcare benefits, tuition assistance, paid time off, holidays, matching 401(k), annual merit, and incentive plans.

    Join us and help write our next chapter.#LI-MO1STERIS 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 (NYSE:
    STE) company with approximately 17,000 associates and Customers in more than 100 countries.

    If you need assistance completing the application process, please call This contact information is for accommodation inquiries only and cannot be used to check application status.

    STERIS is an Equal Opportunity Employer.

    We are 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 (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 § 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.


    Req ID:

    42600 Job Category:
    Engineering
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