Project Engineer III

You're an important part of our future. Hopefully, we're also a part of your future! At

B. Braun, we protect and improve the health of people worldwide. You support this vision, bringing expertise and sharing innovation, efficiency and sustainability as values. That's why we would like to keep developing our company with you. Keeping your future in mind, we're making a joint contribution to health care worldwide, with trust, transparency and appreciation. That's Sharing Expertise.

B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry. Other key product areas include nutrition, pharmacy admixture and compounding, ostomy and wound care, and dialysis. The company is committed to eliminating preventable treatment errors and enhancing patient, clinician and environmental safety.

B. Braun Medical is headquartered in Bethlehem, Pa., and is part of the

B. Braun Group of Companies in the U.S., which includes

B. Braun Interventional Systems, Aesculap and CAPS.

Globally, the

B. Braun Group of Companies employs more than 64,000 employees in 64 countries. Guided by its Sharing Expertise philosophy,

B. Braun continuously exchanges knowledge with customers, partners and clinicians to address the critical issues of improving care and lowering costs. To learn more about

B. Braun Medical, visit

Position Summary:

Works with Engineering, Marketing, Quality, Regulatory, and other key stakeholders to ensure US market and regulatory requirements are met during the design of a product.

Principal Duties Responsibilities:

• Works with cross-functional teams including Marketing, Production, Quality, Regulatory, and R&D to develop design history files (DHF) of medical devices.
• Provide expertise on product design and optimal design specifications.
• Able to lead cross-functional teams to complete medium and large sized projects with moderate management supervision.
• Responsible for interpreting and applying appropriate standards and regulatory guidance to new and existing medical devices.
• Responsible for defining appropriate test strategies and executing testing either internally or with 3rd party vendors.
• Organizes and leads meetings to plan and track project progress.
• Works to quality system regulation design control documents.
• Must comply with applicable ISO and FDA regulations as stated in the Quality Manual.
• Must embody the Company's Vision, Mission and Values.
• Creates 3D models in CATIA V5.
• Transfers Models to 2D drawing.
• Dimension, tolerance and complete drawing to standards
• Other duties may be assigned

Secondary or peripheral job functions:

• Must be able to travel by air and car, and work occasional weekends.
• Requires excellent written and interpersonal communication skills.
• This position requires the handling of instruments that may have been contaminated by blood or other bodily fluids. In compliance with Occupational Safety and Health Administration (OSHA) regulations, Aesculap will provide a safe working environment for all employees.
• Uses professional concepts in accordance with company objectives to help solve complex problems in creative and effective ways, complete projects as assigned and achieve goals.
• Coordinates and supports team activities using creative thinking and organizational skills.
• Works well with intermittent supervision.

Expertise:
Qualifications-Experience/Training/Education/Etc

Required:

• BS in Mechanical Engineering or equivalent required.
• Master's degree in Mechanical Engineering or Biomechanical Engineering preferred.
• General CAD experience. CATIA V5 preferred.
• 5 years industrial experience preferred.

Language and mathematical skills; reasoning ability:

Language Skills:

Ability to read, analyze, and interpret common scientific and technical journals, financial reports, and legal documents. Ability to respond to…