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Principal Engineer, Reagent Engineering

bioMerieux
Bridgeton, MO Full Time
POSTED ON 1/17/2025
AVAILABLE BEFORE 4/7/2025

Position Summary & Responsibilities :

The Principal Engineer, Reagent Engineering will work within the Reagent Engineering Equipment Project team. This team is responsible for the manufacturing equipment used to produce a complex medical device and provides project management and technical expertise related to the manufacturing equipment.

  • Main accountabilities are to lead and manage equipment related projects and to provide Solidworks / AutoCAD expertise related to equipment design / modification.
  • Act as administrator for Solidworks PDM system.
  • Develop documentation such as equipment master records, equipment drawings, parts lists, etc. as required.
  • Manage change control process and other compliance related documentation for projects.
  • Collaborate with Manufacturing, Purchasing, and Quality to lead projects and ensure the optimum manufacturing process in terms of keeping manufacturing moving.
  • Organize and lead meetings as required to support project timelines.
  • Develop and submit CAPEX requests for projects when required.
  • Address unplanned requests for Engineering support as directed by management.
  • Support projects or tasks required to keep manufacturing running and to ensure quality product is being shipped to customers.
  • Evaluate new technologies.
  • Participate in the development of long-term strategies for equipment and process improvements.
  • Drive continuous improvement of manufacturing equipment.

Education, Skills, & Experience :

  • Bachelor’s Degree in a technical field with8 years of engineering experience preferred.
  • High School Diploma with 12 years of engineering experience also accepted

  • Technical Certification / Associates Degree with 10 years of engineering experience also accepted
  • Masters Degree with 5 years of engineering experience also accepted
  • 5 years of experience working with automated processes and machinery.
  • Must have strong ability to use Solidworks / Autocad programs.
  • Solidworks PDM experience is preferred.
  • Project Management experience is preferred.
  • Ability to collaborate professionally in a cross-functional team environment.
  • Knowledge of FDA / ISO regulations and equipment validation is preferred.
  • Strong Knowledge of Microsoft Office (Word, Excel, PowerPoint, and Outlook).
  • Must have strong communication and interpersonal skills.
  • Must have strong analytical and problem-solving skills.
  • LI-US

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