<p>Position Summary</p> <p>The Sr. Molding Engineer will support the ICU Molding Engineering Department. The Sr. Molding Engineer is responsible for owning and driving injection molding improvements through adherence to established product design, scientific injection molding process, tooling, resin, and equipment. The key responsibility of this position is to lead injection molding resources, manage projects within a product family and take action while adhering to defined procedures. The incumbent will also liaise with the Tooling, Molding, Engineering, Production, Quality, and Maintenance departments.</p> <p>Essential Duties & Responsibilities</p> <ul> <li> <p>Functional area tasks and responsibilities</p> </li><li> <p>Day to day</p> </li><li> <p>Represent Molding Engineering to identify possible product modifications to improve manufacturability and impact on automation equipment</p> </li><li> <p>Implement Molding Engineering activities such as scientific injection molding process development, process monitoring, and tool qualifications</p> </li><li> <p>Lead project timelines for Validation (IQ/OQ/PQ) activities and growth/expansion projects</p> </li><li> <p>Initiate and manage projects with adherence to program management guidelines as they relate to new/existing molding equipment, tooling, and materials</p> </li><li> <p>Analyze and spec equipment performance and identify system improvements like vision systems, temperature controllers, robots, and resin analysis</p> </li><li> <p>Implement Cost Savings - Scrap, De-Cavitation, MUV, DPM, OEE</p> </li><li> <p>Close coordination with the resources assigned to the product family (tool room, Process Engr, Quality Engr)</p> </li><li> <p>Own and manage CAPA tasks and deliverables (Corrective and Preventive)</p> </li><li> <p>Coordinate efforts with the Materials Group to assess vendors and provide materials technical information</p> </li><li> <p>Long term expectations</p> </li><li> <p>Lead systematic (Lean / Six Sigma) continuous improvement initiatives like SMED, Jidoka, DMAIC, 5S and STW)</p> </li><li> <p>Maintain Product specifications; consult with manufacturing on product non-conformance</p> </li><li> <p>Perform Design assessments, active participation in Design reviews, Risk Management processes</p> </li><li> <p>Network with senior internal and external personnel</p> </li><li> <p>Intellectual Property review and assessment</p> </li></ul> <p>Knowledge, Skills & Qualifications</p> <ul> <li>Understanding of strength of materials, automation, thermoplastic and LSR injection molding, part assembly, fixturing, testing, and process control techniques </li><li>Risk Management-> FMEA generation </li><li>Six-Sigma Methodology (DOE, Process Capability, Gage R&R, etc.) - use of Minitab Software for analysis </li><li>Knowledge of the Medical Device Industry and familiarity with FDA QSR regulations </li><li>Master Molder training / certification or proof of understanding of the Scientific Injection Molding model; process, tooling, part design, materials, and equipment </li></ul> <p>Education and Experience</p> <ul> <li>Bachelor's degree in Engineering or Technology </li><li>Medical Device Experience is a must </li><li>8 years combined experience in the Medical Device or Engineering Industry </li><li>Advanced Degree may substitute for experience </li></ul> <p>Minimum Qualifications</p> <ul> <li>Must be 18 years of age </li></ul> <p>Travel Requirements</p> <ul> <li>Typically requires travel less than 5% of the time </li></ul> <p>Physical Requirements and Work Environment</p> <ul> <li>While performing the duties of this job, the employee is regularly required to talk or hear. </li><li>This job operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines </li><li>Work is performed in a clean room environment </li><li>While performing the duties of this job, the employee may be required to sit or stand for long periods of time </li><li>Must be able to occasionally move and lift objects of up to 50 lbs </li></ul> <p>ICU Medical has consistently provided you with clinical innovations that help solve real-world challenges.</p> <p>With the acquisition of Hospira Infusion Systems in 2017 and Smiths Medical in 2022, we are now a global market leader with a complete line of clinically-essential IV therapy and high-value critical care products for hospital, alternate site, and home care settings.</p> <p>We're ready to bring you consistent quality, innovation, and value in more areas than ever. Our focus allows us to bring you:</p> <ul> <li>Dedicated and non-dedicated IV sets and needlefree connectors clinically proven to provide an effective barrier against bacterial transfer and colonization. </li><li>The industry's broadest IV smart pump offering covering large volume, pain management, and ambulatory needs. </li><li>IV medication safety software providing full IV-EHR interoperability with the highest customer satisfaction and compatibility with more EHR systems than any other company. </li><li>Significant US IV solutions manufacturing and supply capabilities. </li></ul> <p>ICU Medical EEO Statement:</p> <p>ICU Medical is committed to being an Equal Opportunity Employer. We ensure that all qualified applicants receive fair consideration for employment regardless of race, color, nationality or national origin, ethnicity, sex, gender, religion or belief, marital or civil partnership status, sexual orientation, pregnancy or maternity, age, disability, or protected veteran status.</p> <p>If you are an individual with a disability and need reasonable accommodation to participate in the employment selection process, please contact us at humanresources@icumed.com. We are committed to providing equal access and opportunities for all candidates.</p> <p>ICU Medical EEO Policy Statement</p> <p>Know Your Rights: Workplace Discrimination is Illegal Poster</p> <p>ICU Medical CCPA Notice to Job Applicants</p>