Biomerics

Injection Molding Process Engineer

Biomerics  •  Mebane, NC (Onsite)  •  4 hours ago
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Job Description

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.

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.

Biomerics

About Biomerics

Founded in 1994, Biomerics is the leading vertically integrated medical device contract manufacturer serving the interventional device market. Trusted as a vertically integrated partner with extensive engineering expertise and solutions, Biomerics supplies 20 of the top 30 medical device OEMs globally. Biomerics provides engineering design and development services, technology transfer manufacturing services and contract manufacturing services — including sterilization and packaging — for medical device components, subassemblies and finished medical devices. Through nine locations in the United States, two locations in Costa Rica, one in the Dominican Republic and one in Ireland, Biomerics meets customers’ immediate and long-term strategic needs. With comprehensive engineering Centers of Excellence, Biomerics is a leader in materials, interventional medical plastics, complex extrusion, micromachining of metals and polymers, laser processing, guidewires, balloons and balloon catheters, advanced catheters and steerables, image guided intervention, micro-overmolding, micro precision stamping, complex microassembly and finished device assembly. In addition to operating under a certified ISO 13485:2016 quality system, Biomerics is FDA registered and compliant with FDA 21 CFR Part 820.

Markets we serve:

* Cardiovascular

* Endoscopy

* Neuromodulation

* Neurovascular

* Robotic Surgery

* Structural Heart

* Urology

* Vascular Access

Industry
Manufacturing & Production
Company Size
1,001-5,000 employees
Headquarters
Salt Lake City, Utah
Year Founded
1994
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