About Meridian

Meridian Bioscience is a fully integrated life science company that develops, manufactures, markets and distributes a broad range of innovative diagnostic products. We are dedicated to developing and delivering better solutions that give answers with speed, accuracy and simplicity that are redefining the possibilities of life from discovery to diagnosis. We are looking for talented and passionate individuals that help drive our vision. Our innovative culture will allow interested candidates to discover and create, through collaboration, cutting edge solutions to tough problems.

Job Summary

The Process Engineer is responsible for equipment/automation/process design, procurement, fabrication, and troubleshooting.

Key Duties

• Equipment procurement
  • Assists other Engineers in the identification and procurement of manufacturing equipment and automation.
  • Ensures completion of design documentation (URS, FAT, and SAT) for new equipment procurement according to internal procedures and in accordance with industry standards (GAMP, ASTM E2500)
  • Identifies, qualifies, and works with equipment vendors.
  • Leads cross functional procurement team.
  • Performs project management activities to ensure projects are on time, within budget, and successful.
• Validation
  • Supports validation engineers for equipment qualification through training and test case design.
  • Author, obtain appropriate approvals, and perform validation studies as needed.
• Maintenance
  • Support maintenance staff to service equipment as needed.
  • Supplies troubleshooting support to help identify the causes of product/production related problems.
  • Design and implement process improvements and corrective actions.
• Process Design
  • Designs and implements manufacturing equipment solutions to improve operational efficiencies.
  • Supports production teams for new equipment and automation solutions for improved processes or for new products from R&D
• General
  • Read, understand, and comply with Good Manufacturing Practices and Standard Operating Procedures and accurately complete all required documentation per SOP requirements.
  • Perform all duties in accordance with safety rules as well as appropriate industry and regulatory guidelines.
  • Communicates clearly and effectively with department peers, manufacturing personnel, as well as supervisors, managers, and directors.
  • Assist and train employees on proper equipment operation.
  • Write and/or modify manufacturing and equipment related procedures as needed
  • Update and maintain facility maps
  • Other duties as assigned.

Qualifications

Education/Experience:

• Requires a Bachelor’s degree in a Science or Engineering field with a minimum of two years of experience in a related field.
• Previous experience with RSLogix/Studio 5000, machine vision (Keyence/Cognex), HMI programming is desirable
• Previous experience in equipment procurement and/or process support and design is desirable
• Previous experience in and FDA regulated production environment is desirable.

Skills, Specialized Knowledge and Abilities:

• Must possess a working knowledge of the Metric System
• Advanced computer skills required (Word, Excel, CAD knowledge, PLC Database).
• Proficient in CAD. Solidworks and AutoCard experience preferred.
• Proficient in programming, specifically industrial control systems and ladder logic. RSLogix 5000 preferred.
• Thorough knowledge of electrical control systems.
• Proficient mechanical skills using diagnostic tools used to test, troubleshoot and repair complex equipment.
• Ability to read/understand blueprints, schematics, wiring diagrams and other specialized documentation.
• Ability to read, understand and follow all company Standard Operation Procedures (SOPs) and guidelines.
• Adhere to safety SOPs and report potential safety hazards.
• Must have strong math skills.
• Must be a self starter, detail oriented, organized and able to perform under pressure in a fast-paced environment with minimal supervision.
• Excellent interpersonal, organizational, written and oral communication skills.
• Ability to maintain regular attendance and punctuality requirements.
• Must be able to work overtime and weekends to support production efforts as needed.
• Must be able to work independently as well as collaboratively in a team setting with peers in a cross functional setting.
• Excellent analyzing, problem solving and troubleshooting skills.

Requirements (Physical, Mental, Environmental Demands):

• Ability to walk up and down several flights of stairs throughout the work day in a multi-location facility.
• Must be able to lift 40 pounds routinely throughout the course of a work day.
• Must be able to wear personal protective equipment (latex or nitrile gloves, face shield/safety glasses, hairnets, shoe coverings, etc.).
• Must have fine manual dexterity to ensure precise assembly of medical devices.
• Must be able to adhere to applicable biosafety practices when on the manufacturing floor or in laboratories.
• Ability to stand for long periods of time, stoop, reach, push and pull equipment throughout the course of the work shift.
• Ability to work on PC including repetitive use of a keyboard and mouse for long periods throughout the course of the work day
• May be required to sit for long periods of time through the course of the work shift.
• Must be able to analyze and interpret data.
• Must be able to concentrate and problem solve routinely throughout the course of the work shift.
• Must be able to differentiate colors in product.
• Must be able to detect audible alarms
• Must be able to travel by car/air to other locations of MBI as needed.

We are proud to be an EEO/AA employer Minority/Female/Disability/Veteran. We maintain a drug-free workplace and perform pre-employment substance abuse testing.