STERIS Corporation

Process Manufacturing Engineer I

STERIS Corporation$78K — $101K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in Engineering
  • 3 years of relevant experience in process manufacturing
  • Familiarity with FDA and cGMP requirements
  • Experience with process improvement methodologies
  • Ability to develop and execute design of experiments (DOE)

Responsibilities

  • Support FDA and cGMP protocols for equipment qualification and validation
  • Develop and implement lean principles in manufacturing processes
  • Create experimental plans for new and reformulated products
  • Collaborate with Product Development and Production teams
  • Research and test new manufacturing technologies
  • Establish operating set points for process controls
  • Conduct process studies and implement improvement opportunities

Benefits

  • Market Competitive pay
  • Extensive Paid Time Off and Holidays
  • Excellent Healthcare, Dental and Vision benefits
  • Long- and Short-Term Disability coverage
  • 401(k) with company match
  • Maternity and Paternity Leave
  • Tuition Reimbursement and continuing education programs
  • Opportunities for advancement in a stable, long-term career
Full Job Description
Position Summary

The Process Manufacturing Engineer I in our St. Louis, MO location is responsible for establishing the manufacturing process capability for new/reformulated products. In this role you will support the execution of equipment qualification, cleaning, and process validation program. Prepare and revise batch records, operating instructions, and cleaning instructions. 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, and operators as required. Develop P&D's in support of validation efforts. Develop design of experiment (DOE) for the purpose of scale-up, troubleshooting and modifications of new and existing processes.

What You'll Do as a Process Manufacturing Engineer

  • Support the execution of protocols to comply with FDA and cGMP requirements for equipment qualification, cleaning and process validations.
  • Responsible for the development of lean culture and institution of lean principles.
  • Develop plans, design experiments, and schedules for establishing manufacturing process capability and introduction of new/reformulated products.
  • Interface with Product Development and Production to bring these processes from the research laboratory through scale-up full-scale manufacturing.
  • Responsible for research and testing of new technologies or processes appropriate for support of new/existing product manufacture.
  • Establish and maintain set point controls.
  • 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/equipment.
  • Responsible for conducting process studies, identifying opportunities for improvement and supporting implementation of findings to optimize liquid blending systems.
  • Resolve manufacturing deficiencies through troubleshooting and implementation of corrective actions.


The Experience, Skills, and Abilities Required

  • Bacehlor's Degree in Engineering
  • Minimum of 3 years of related experience required.


What STERIS Offers

We value our employees and are committed to providing a comprehensive benefits package that supports your health, well-being, and financial future.

Here is just a brief overview of what we offer:
  • Market Competitive pay
  • Extensive Paid Time Off and added Holidays
  • Excellent Healthcare, Dental and Vision benefits
  • Long- and Short-Term Disability coverage
  • 401(k) with a company match
  • Maternity and Paternity Leave
  • Additional add- on benefits / discounts for programs such as Pet Insurance
  • Tuition Reimbursement and continuing education programs
  • Excellent opportunities for advancement in a stable long-term career

#LI-BN1

Pay range for this opportunity is $78,200.00 - $101,200.00. 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.

About STERIS Corporation

STERIS Corporation is a leading provider of infection prevention and other procedural products and services. The company was founded in 1985 and is headquartered in Mentor, Ohio. STERIS offers a wide range of products and services, including sterilization systems, surgical tables, and cleaning and disinfection products. The company has operations in over 100 countries and serves customers in the healthcare, pharmaceutical, and research industries. STERIS has been recognized for its commitment to sustainability and has received several awards for its environmental initiatives.
Learn more about STERIS Corporation
Size
16,422 employees
Market Cap
$18.2 billion
Industry
Net Income
$431.8 million
Founded
1985
5 Year Trend
+11.9%
Revenue
$3 billion
NASDAQ

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