Senior Manufacturing Engineer
TLDR
As a key member of the operations team, you will improve manufacturing processes and design transfer activities for new medical devices in a fast-paced environment.
- Design manufacturing processes, procedures, and production layouts to optimize productivity, maintainability, and cost for drug-device combination products.
- Optimize drug coating, manufacturing, and packaging processes, improve process capabilities, prioritize process improvement opportunities, and innovate and implement process improvements on platform or derivative projects.
- Actively participate in PFMEA, DFMEA, Process Mapping, and Critical to Quality (CTG) reviews assuring specifications are well defined and documented; participate/lead Design for Manufacturing (DFM) activities to verify manufacturability of Product Designs.
- Manage and support line validation/qualification activities including IQ, OQ, MSA and PQ, including authoring all related documentation and execution of testing protocols.
- Actively participate in Lean initiatives to stabilize production lines, reduce waste, and improve manufacturing efficiency. Calculate production, labor, and material costs and review production schedules to make data-based decisions for improvements.
- Create and review process flow charts, production tooling strategies, production line layouts, production capacity analysis, and EHS project plans.
- Prepare documentation including: testing protocols for product evaluations, work instructions, Control Plans, Manufacturing Processes, job safety analysis sheets, and product and process reports.
- Master's degree, or equivalent, in Biomedical, Mechanical, or Industrial Engineering or related field, and 5 years relevant experience, or Bachelor's degree and 8+ years relevant experience
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Experience must include:
- Manufacturing, quality, and product development
- Experience with catheters, balloon catheters, bonding processes, including manufacturing and testing processes
- Preferred knowledge of combination medical devices and injection molding processes
- Working with ISO 13485/ISO 9001
- Working within a controlled medical device environment
- Proven experience and knowledge in design controls, device design and development standards, FDA regulation, GMP practices and QSR requirements
- Project management skills including development of project plans, schedules and budgets, including strong communication skills, ability to manage communication with cross functional teams and external contractors and ability to effectively present technical information.
- Working knowledge of DFM (Design for Manufacturability), Six Sigma, and Lean manufacturing practices.
- Strong hands-on technical aptitude, with ability to troubleshoot equipment, recommend corrective actions and implement solutions
- Approximately 10%-25% domestic and/or international travel required.
- Green Belt certification and Lean Six Sigma certifications
- Knowledge of technology transfer/product line transfer
- Paid time off and paid volunteer time
- Medical, Dental, Vision and Flexible Spending Account
- Health Savings Account with Company Funded Contributions
- 401k Retirement Plan with Company Match
- Parental Leave and Adoption Services
- Health and Wellness Programs and Events
- Awarded 2024 Cigna Healthy Workforce Designation Gold Level
Benefits
Health Insurance
Medical, Dental, Vision and Flexible Spending Account
Home Office Stipend
Health Savings Account with Company Funded Contributions
401k with company match
401k Retirement Plan with Company Match
Paid Parental Leave
Parental Leave and Adoption Services
Paid Time Off
Paid time off and paid volunteer time
Wellness Stipend
Health and Wellness Programs and Events
Laborie Medical Technologies Corp develops and advances specialized medical technologies focused on preserving and restoring human dignity. Their innovative solutions cater to healthcare providers, aiding in safe deliveries and the treatment of pelvic and gastrointestinal conditions.