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Internship Mems Process Engineer Jobs in Missouri

Manufacturing Engineer

Chesterfield, MO · On-site

$72K - $93K/yr

What's the role? The Manufacturing Process Engineer is responsible for driving manufacturing ... internship capacity within a manufacturing, production, or industrial environment. * Exposure to ...

By submitting your interest, you'll be among the first to know when internship opportunities open ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

By submitting your interest, you'll be among the first to know when internship opportunities open ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

By submitting your interest, you'll be among the first to know when internship opportunities open ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

By submitting your interest, you'll be among the first to know when internship opportunities open ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

By submitting your interest, you'll be among the first to know when internship opportunities open ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

By submitting your interest, you'll be among the first to know when internship opportunities open ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

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Internship Mems Process Engineer information

What is the difference between Internship Mems Process Engineer vs Mems Process Engineer?

AspectInternship Mems Process EngineerMems Process Engineer
QualificationsEnrolled in or recent graduate of engineering or related programBachelor's or higher in engineering, with experience preferred
Work EnvironmentInternship setting, often in R&D labs or manufacturing facilitiesFull-time professional role in MEMS fabrication or design
ResponsibilitiesAssisting process development, learning fabrication techniquesDesign, optimize, and troubleshoot MEMS manufacturing processes
Industry UsageEntry-level, educational focus, training periodOperational, development, and production tasks in MEMS industry

The main difference between an Internship Mems Process Engineer and a Mems Process Engineer is experience level and scope. Internships are educational roles for students or recent graduates, focusing on learning and assisting, while Mems Process Engineers are full-time professionals responsible for designing and improving MEMS manufacturing processes.

What are the most commonly searched types of Mems Process Engineer jobs in Missouri? The most popular types of Mems Process Engineer jobs in Missouri are:

Senior Process Manufacturing Engineer

American Sterilizer Company (US)

Saint Louis, MO • On-site

$101K - $130K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted yesterday


Job description

Position Summary

The Senior Process Manufacturing Engineer in our St. Louis, MO location is responsible for establishing themanufacturing process capability for new/reformulated products. In this role you will support the execution ofequipment qualification, cleaning, and process validation program. Prepare and revise batch records, operatinginstructions, and cleaning instructions. Conduct process improvement studies in the areas of operationalproductivity, process control, quality processing, employee safety, process yield improvement, and environmentalimpact in a lean environment. Test new technologies, processes, controls or prototype equipment and supportimplementation as appropriate to optimize liquid blending systems. Provide indirect supervision of technicians,interns and operators as required. Develop P&ID'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.


This position requires that you work onsite Monday through Friday during core business hours in our St. Louis, MO location.

What You'll do as a Senior 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 andintroduction of new/reformulated products.
  • Interface with Product Development and Production to bring these processes from the research laboratorythrough scale-up full-scale manufacturing.
  • Responsible for research and testing of new technologies or processes appropriate for support ofnew/existing product manufacture.
  • Establish and maintain set point controls.
  • Support Project Engineering to obtain approval for Capital Appropriation Requests, design specifications andequipment installation.
  • Provide personnel training, development of manufacturing instructions and start-up of newprocesses/equipment.
  • Responsible for conducting process studies, identifying opportunities for improvement and supportingimplementation of findings to optimize liquid blending systems.
  • Resolve manufacturing deficiencies through troubleshooting and implementation of corrective actions.
  • Develop and submit written reports including objective, experimental, compilation of data, engineeringanalysis, conclusions and recommendations.
  • Monitor and provide solutions in terms of quality, yields, throughput, cycle times, process parameters, cGMPcompliance, and safety and environmental requirements.
  • Apply structured, technical problem-solving methodologies such as DMAIC, six sigma green belt/black beltstatistical analysis, etc. to confirm root causes of problems.
  • Implement corrective and preventative actions to solve root causes and prevent recurrence, reduce variation,and drive improvement in quality and other key KPI's.
  • Serve as Subject Matter Expert (SME) providing deep technical insights into operations processes, includingchemical and biological formulation, filling, packaging, and quality operations.
  • Employ key project management principles including establishing and tracking timelines, identifying andmitigating risks, communicating across teams at all levels.
The Experience, Skills and Abilities Needed

Required:

  • Bachelors degree in Engineering.
  • Minimum five (5) years in process engineering or equivalent.
  • Background in biochemical or chemical engineering, or microbiology.
  • Project leadership skills, technical skills, and organization skills required.
  • Experience with FDA, and GMP regulated operations, such as Medical Devices or PharmaceuticalManufacturing.
  • Good communication skills and interpersonal skills.
  • Proven proficiency in facilitating problem solving and other team-based root cause analysis (RCA).
  • Ability to generate detailed, high quality technical documentation to capture and communicate designs.
  • Ability to influence team members to perform at exceptional levels.

Preferred:

  • Lean Six Sigma certification such as Green Belt or Black Belt, preferred.
What STERIS Offers

We value our employees and are committed to providing a comprehensive benefits package that supports yourhealth, 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

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Employment Type: FULL_TIME