SENIOR MECHANICAL ENGINEER (ASSOCIATE PRINCIPAL) INSTRUMENT MANUFACTURING

WE SAVE LIVES!! At BioMrieux, we make medical diagnostic equipment that is vital to maintaining world health. The solutions that our teams imagine, develop and manufacture are key to enabling healthcare professionals and industry players in making confident decisions to improve patient outcome and ensure consumer safety.

Be a part of the team that is responsible for sustaining the manufacture of this life saving equipment. You will be working in a dynamic and highly regulated environment with a cross functional team including engineering, production, quality assurance, purchasing, logistics, and others.

BioMrieux is committed to an inclusive working atmosphere that fosters professional growth for our valued employees. We are looking for self-starters with a passion for knowledge and helping others.

Come to BioMrieux and be a part of our team!

Position Summary :

Perform all aspects of mechanical design from the initial feasibility stage to manufacturing release for use in medical diagnostic equipment.

Using knowledge of electro-mechanical components, design for manufacturing, drawings, inspections, and CAD. Supports and optimizes instrument manufacturing activities.

Provide SME support for existing product lines.

Primary Duties :

• Lead in the definition, proof of concept, development, implementation and / or support of mechanical designs to support department projects and objectives in the manufacture of medical devices.
• Troubleshoot and utilize problem-solving tools to resolve issues with process and / or product.
• Remain current on technological advancement in the relevant area of expertise.
• Ensure quality of deliverables by following the appropriate design practices and departmental procedures for design control and regulatory compliance.
• Create appropriate documentation such as technical communications, reports, meeting notes, change management, and other relevant technical documentation.
• Prioritize activities within the scope of the assignments to ensure schedules and quality of work is successfully achieved.
• Participate in material planning activities.
• Perform reviews related to risk analysis, change control, verification, validation, and other functions within the department.
• Define, review, and check product Bill of Materials (BOM), assembly instructions, and test procedures for implementation into Manufacturing.
• Work cross functionally with internal departments and lead project teams.
• Mentor less experienced team members to facilitate technical development and increase knowledge of business practices.

Studies and Experience :

• Bachelor's of Science in Mechanical or Biomedical Engineering with 8+ years of engineering experience OR Masters of Science in Mechanical or Biomedical Engineering with 5+ years of engineering experience (if no degree, 13 years of relevant experience performing engineering functions)
• Experience in electro / mechanical production processes.
• Knowledge and experience in Lean Manufacturing techniques and production processes.
• Technical skills in the relevant Manufacturing Engineering disciplines.
• Experience managing large scale projects requiring multiple team members and launch schedules beyond 6 months.
• Experience with FDA, QSR and ISO quality systems. (preferred)

Knowledge, Skills, and Abilities :

• Organization, timeliness, and quality of technical development activities.
• Quality and completeness of documentation.
• Development of personal autonomy and time management skills with the ability to handle multiple assignments and tasks.
• Knowledge of CAD (SolidWorks, Creo, NX), PLM (Windchill), and ERP systems (SAP)
• Knowledge of electro / mechanical production processes.
• Ability to articulate complex technical concepts to a non-technical audience.
• Ability to communicate with team members and other groups effectively
• Proficiency in Microsoft Office applications (Word, Excel, Power Point, and Project)

Job ID : 37461