Senior Manufacturing Engineer
About The Position
IRP Medical is seeking a Senior Manufacturing Engineer specializing in medical device components, with deep expertise in LSR and EPDM processing, automation, and scalable production in regulated cleanroom environments. Proven ability to lead process development, validation (IQ/OQ/PQ), and continuous improvement initiatives. IRP Medical is a trusted leader in engineered elastomer solutions serving Medical Device, and aerospace markets. Our team designs and manufactures precision-molded seals, gaskets, and custom rubber components that perform in the most demanding environments. We take pride in craftsmanship, collaboration, and a culture built on innovation and reliability.
Requirements
- Bachelor’s Degree in Engineering or minimum 6 years of experience in a technical capacity in an injection molding environment
- Experience in liquid silicone rubber, EPDM and rubber molding in general
- Process Automation Experience
- Direct Experience with MRP
- Possessing Critical Interpersonal skills so as to Function effectively in a Team Environment
- Excellent oral and written communication
- Microsoft Office (Excel, PowerPoint, Project, and Word)
Nice To Haves
- CAD Experience
- Lean Six Sigma experience
- Experience working with 3 axis robots
- Bilingual English/Spanish
Responsibilities
- Lead the development, optimization, and validation of manufacturing processes for medical device components utilizing Liquid Silicone Rubber (LSR) and EPDM materials
- Drive automation initiatives, designing automated solutions to reduce manual labor and improve process consistency and throughput. Integration of robotic systems, vision systems, and automated assembly equipment.
- Partner with tooling and equipment vendors to design and procure molds, fixtures, and automation systems tailored to elastomer processing
- Design and implement robust, scalable manufacturing processes that meet stringent regulatory and quality requirements (e.g., FDA, ISO 13485)
- Support new product introduction (NPI) by ensuring designs are manufacturable, scalable, and compliant with medical device standards and risk management requirements
- Develop and execute process validation protocols (IQ/OQ/PQ), ensuring full traceability and compliance with regulatory expectations
- Create and maintain comprehensive documentation, including process flows, PFMEA, control plans, validation reports, and standard operating procedures (SOPs)
- Optimize LSR and EPDM molding processes (injection and compression), including material handling, mixing, curing, and post-processing, with a focus on consistency and biocompatibility
- Troubleshoot and resolve complex issues related to molding defects, contamination, tooling wear, and process variability in controlled environments
- Collaborate with Quality and Regulatory teams to support audits, CAPA investigations, nonconformance resolution, and change control processes
- Specify, source, and qualify molds, tooling, and automated equipment, ensuring compatibility with cleanroom and medical-grade production requirements
- Implement in-line inspection and validation technologies, including vision systems and automated testing for critical-to-quality (CTQ) features
- Support maintenance teams with preventive and predictive maintenance strategies for manufacturing equipment
- When requested, helps to train production operators and technicians in the manufacture of more complex parts and assemblies.
Benefits
- medical
- dental
- vision
- short and long-term disability coverage
- accident insurance
- critical illness insurance
- basic and supplemental life insurance
- employee assistance plan
- retirement savings and matching
- other developmental opportunities
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What This Job Offers
Job Type
Full-time
Career Level
Senior
