Manufacturing Engineer II

1 Month ago • 3-5 Years • Software Development & Engineering

Job Summary

Job Description

This Manufacturing Engineer II position supports the consumable manufacturing process within a cross-functional team, focusing on optimizing product performance and troubleshooting manufacturing processes. The role involves partnering with internal teams and vendors to implement best practices in medical device manufacturing, identify root causes of problems, and recommend solutions. Key responsibilities include supporting various aspects of the consumable product manufacturing process, analyzing data to determine product performance, building internal and external relationships, performing maintenance on manufacturing equipment, assisting with NCR investigations, and generating technical documentation. The engineer will also execute validation of new equipment and processes in compliance with FDA standards and work in a cleanroom environment.
Must have:
  • Bachelor's in engineering or related discipline
  • 3-5 years of experience with Bachelor's degree
  • 1-3 years of experience with Master's degree
  • Manufacturing Engineering support
  • CAD/Solidworks
  • Inspection
  • Failure investigation
  • Technical writing
  • Process validation
  • Familiarity with FDA standards
Good to have:
  • Film and plastic bonding and sealing
  • Filling
  • Sheet metal design
  • Materials knowledge
  • Pneumatics
  • Machining (esp. CNC)
  • GD&T
  • SPC
  • PLC
  • Microfluidics
  • Thermal characterization
  • Vacuum physics
  • Heat and mass transfer
  • Electrical Schematics
Perks:
  • Some travel required

Job Details

Description

Position Summary

This engineer works on a cross-functional Manufacturing Engineering team to support several aspects of the consumable manufacturing process. Partners with internal team members and vendors to optimize product performance.  Performs troubleshooting and routine maintenance of basic to moderate manual and automated manufacturing processes.  Leverages experience and skillset to implement best practices within the realm of consumable medical device manufacturing by identifying root causes and recommending solutions. Contributes to the resolution of basic to moderate manufacturing engineering problems.

 

Primary Duties

  • Perform all work in compliance with company policy and within the guidelines of bioMerieux’s Quality System.
  • Supports several aspects of consumable product manufacturing process.
  • Works with senior engineers and vendors to optimize product performance.
  • Collects and analyzes data to determine performance of the product with minimal supervision.
  • Builds relationships both internally and externally as a member of a cross-functional team.
  • Troubleshooting and routine maintenance of manufacturing equipment.
  • Assisting with NCR investigations, write-ups, and product dispositions.
  • Implements best practices and corrective actions.
  • Participates on team performing FMEA to identify root causes of problems and present possible solutions.
  • Contributes to solving moderate manufacturing engineering problems.
  • Makes design and technical recommendations subject to review by Manufacturing Engineering Manager.
  • Generates variety of technical documentation including WIDs, technical reviews, studies.
  • Performs primary duties in a clean room environment.
  • Executes validation of new equipment and processes consistent with FDA standards.
  • Makes design and technical decisions subject to review by Senior, Principal, and other engineers.
  • Performs other duties as assigned.

 

Supplemental Data

  • Travel: some travel required.
  • Team: usually works on a team with several technicians, engineers and a project manager.

 

Training, Education and Experience

  • Bachelor’s in engineering or related discipline.
  • 3-5 years of experience in related field with a Bachelor’s degree, or 1-3 years of experience in related with a Master’s degree, and including performance consistent with said experience.

 

Knowledge, Skills and Abilities

  • Manufacturing Engineering Support of Manufacturing Equipment:
    • CAD/Solidworks
    • Inspection
    • Failure investigation
    • Technical writing
  • Experience with the following is preferred:
    • Film and plastic bonding and sealing
    • Filling
    • Sheet metal design
    • Materials (e.g. plastics, aluminum, copper, steel, etc.)
    • Pneumatics
    • Machining (esp. CNC)
    • GD&T
    • Process validation
    • Familiarity with FDA standards
    • SPC
  • Experience with the following is desirable:
    • PLC
    • Microfluidics
    • Thermal characterization
    • Vacuum physics
    • Heat and mass transfer
    • Electrical Schematics

 

Working Conditions and Physical Requirements

  • Ability to remain in stationary position, often standing, for prolonged periods.
  • Ability to adjust or move objects up to 50 pounds in all directions.

 

Please be aware that recruitment related scams are on the rise. Fraudulent job postings are being placed on other websites, and individuals posing as bioMérieux Talent Acquisition team members are reaching out via email or text message in an attempt to collect your personal and confidential information. In some cases, these scammers are also conducting bogus interviews prior to extending fraudulent offers of employment. Beware of individuals reaching out using general phone numbers and non-bioMerieux email domains (i.e. Hotmail.com, Gmail.com, Yahoo.com, etc.). If you are concerned that an interview experience or offer of employment might be a scam, please make sure you are searching for the posting on our careers site https://careers.biomerieux.com/ or contact us at recruitment@biomerieux.com.

BioMérieux Inc. and its affiliates are Equal Opportunity/Affirmative Action Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. Please be advised that the receipt of satisfactory responses to reference requests and the provision of satisfactory proof of an applicant’s identity and legal authorization to work in the United States are required of all new hires. Any misrepresentation, falsification, or material omission may result in the failure to receive an offer, the retraction of an offer, or if already hired, dismissal. If you are a qualified individual with a disability, you may request a reasonable accommodation in BioMérieux’s or its affiliates’ application process by contacting us via telephone at (385) 770-1132, by email at recruitment@biomerieux.com, or by dialing 711 for access to Telecommunications Relay Services (TRS).

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