Medical Project Engineer Position Available In St. Louis, Missouri

Medical Project Engineer 3.3 3.3 out of 5 stars 3433 Tree Court Industrial Boulevard, Kirkwood, MO 63122

Shift:

7:45 AM

• 4:15 PM (Monday
• Friday)

Location:

St. Louis, MO (On-site) Seiler Instrument & Mfg. Co., Inc. is looking for a detail-oriented and solutions-driven Medical Project Engineer to join our team! If you excel in project management, collaboration, and medical device design, we want to hear from you. This is a great opportunity to apply your technical expertise in a company that values innovation, quality, and teamwork. Apply today and be part of a team where your skills make a real impact! Why Join Seiler? At Seiler, we’re dedicated to producing top-quality medical systems while prioritizing the well-being of our employees. Here’s what we offer: Comprehensive Benefits (Medical, Vision, Dental) Parental & Bonding Leave Paid Time Off (PTO) 401(k) Matching & Profit Sharing Tuition Reimbursement 9 Paid Holidays Employee Assistance Program (EAP) Summer Company Events (1-2 free events annually) Flexible Start/Stop Times for Most Positions What You’ll Do Manage Project Timelines

• Effectively manage and oversee the product development timeline, ensuring projects are delivered on schedule and meet all technical and quality benchmarks. Lead Product Design
• Utilize your skills in Autodesk Inventor, SOLIDWORKS, or similar CAD software to enhance product design and development. Your experience in working with detailed product models is essential for solving complex issues with support from consultants and innovating our device lineup. Collaborate Across Teams
• Facilitate communication and integration of project management practices and product modeling techniques across various teams Work with Vendors & Suppliers
• Collaborate with vendors and suppliers to ensure timely delivery of materials and services Ensure Regulatory Compliance
• Maintain responsibility for ensuring that all projects adhere to relevant regulatory standards, including

ISO:

13485 and global regulations for Class 1 medical devices. Obtain ISO Lead Auditor Certification. Manage vendor relationships and issue corrective actions when required. Maintain Technical Documentation

• Lead the creation and updating of comprehensive technical documents, ensuring they reflect all project and regulatory necessities. Conduct Audits & Record-Keeping
• Conduct thorough audits and maintain detailed records to guarantee the integrity and compliance of all project and product modeling endeavors.

What We’re Looking For Bachelor’s degree in Mechanical Engineering (preferred) Strong Project Management with Complex Projects and Timelines Skills Proficiency in CAD Software (Autodesk Inventor, SOLIDWORKS) Understanding of Medical Device Regulations (ISO 13485) Excellent Communication & Collaboration Skills and Foster Collaboration and Communication Across Diverse Teams Experience in Vendor & Supplier Management Technical Documentation & Auditing Skills