Injection Molding Process Engineer at Biomerics

Mebane, North Carolina, United States -

Full Time

Start Date

Immediate

Expiry Date

18 Sep, 26

Salary

0.0

Posted On

20 Jun, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Scientific Injection Molding, Process Validation, DFM, Project Management, SolidWorks, Minitab, Statistical Analysis, Root Cause Analysis, pFMEA, dFMEA, IQ/OQ/PQ, Technical Writing

Industry

Medical Equipment Manufacturing

Description

Description Company Overview Biomerics is a world-class manufacturer and innovative polymer solutions provider for the medical device and biotech industries. As a vertically integrated company, we specialize in designing, developing, and producing medical devices for diagnostic and interventional procedures. We are focused on next-generation solutions for vascular access, electrophysiology, cardiac rhythm management, neurovascular, structural heart, and cardiovascular markets. At Biomerics, we are dedicated to our diverse employee base. We understand that a strong, skilled, and engaged workforce is the foundation of our continued success as a business. We strive to live up to Biomerics' values in all our interactions. It is an exciting time to be part of our collective team, and there is no limit to the impact that can be achieved here at Biomerics. We improve and advance the lives of our employees and the patients who depend on our products. At Biomerics, we believe in integrity, partnership, empowerment and accountability, trust, agility, teamwork, and excellence, and we care. Our team-oriented, customer-focused corporate culture prioritizes building strategic, mutually beneficial partnerships with customers and our team members. Job Summary As an Injection Molding Process Engineer, you will provide technical expertise in support of existing operations and new product development and introduction projects. You will establish and maintain manufacturing processes and procedures, including capacity planning, tooling acquisition, replacement plans, process development using scientific injection molding techniques, routings, cost reductions, and quality improvements within the organization. A special focus is placed on Injection Molding, new tool specification, acquisition, debugging, decoupled process development, validation, and new or replacement equipment specification and activities. Key metrics for this position include project on-time delivery, scrap, machine efficiency, cost reductions, and customer satisfaction. Potential relocation assistance available for our final candidate, if needed. Roles and Responsibilities Include: Responsibilities Establishing project timelines and driving for the successful completion of projects. Direct interface with customers, suppliers, and internal resources in a professional manner. Defining and managing the scope, time, budget, and resources of projects. Coordinating DFM (Design for Manufacturability/Moldability) with other engineers, external vendors, customers, and internal project teams. Leading the validation activities to launch new products and molds into production, including all documentation in accordance with company, FDA, ISO, and customer standards. Managing all molding validation activities, including developing validation plans, writing protocols and reports, coordinating metrology and inspections, and communicating with customers. Submit, review, and/or approve change orders to implement new or revised existing processes. Train production personnel on new and revised processes. Technical writing of protocols, reports, work instructions, etc. Any other duties or projects as required. Requirements A minimum of five (5) years of related work experience (preferably in the medical device field). B.S. degree in an engineering or related field or equivalent experience (Plastics, mechanical, manufacturing, or materials preferred). Experience developing injection molding processes using Scientific Injection Molding principles. Experience specifying and procuring Injection Molding Tooling, Molding Machines, and Auxiliary Equipment. Strong verbal and written communication skills. Proficiency in project management software (e.g., MS Project, Smartsheet, Excel, or similar) Beginning experience level in SolidWorks. Proficiency in Microsoft Office (e.g. Word, Excel, PowerPoint, etc.). Must be able to work in a fast-paced environment with little to no supervision. Experience with medical process validation, including validation definition and execution (IQ, OQ, PQ), test method definition, root cause analysis, and measurement systems analysis (MSA), pFMEA, dFMEA. The ability to perform statistical analysis (DOE, capability, GR&R, etc.) using Minitab software. Experience and understanding of the development and design of plastic parts and assemblies preferred. Benefits: Biomerics offers Medical/Dental/Vision Insurance, Short-Term Disability, Long-Term Disability, Life Insurance, Paid Vacation Days, 9 Paid Holidays, 401k, and an Onsite Fitness Facility. Biomerics does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on Biomerics’ approved agency list. Unsolicited resumes or candidate information submitted to Biomerics by search/recruiting agencies not already on Biomerics’ approved agency list shall become the property of Biomerics. If Biomerics subsequently hires the candidate, Biomerics shall not owe any fee to the submitting agency.

Responsibilities

Provide technical expertise for existing operations and new product development focusing on injection molding processes and tooling acquisition. Lead validation activities, manage project timelines, and coordinate DFM with customers and internal teams.