Injection Molding Process Engineer

Staffing Network LLC

Winston-Salem (NC)

On-site

USD 90,000 - 120,000

Full time

6 hours ago
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Benefits offered by this job

Relocation assistance

Job summary

Staffing Network LLC in Winston-Salem, NC, is seeking an Injection Molding Process Engineer to provide technical expertise in support of existing operations and new product development, establishing and maintaining molding processes, tooling, and qualification activities.

You will drive process development, capacity planning, and cost reductions, coordinate with customers and suppliers, and lead validation and documentation in line with FDA/ISO and customer standards.

Qualifications

  • Minimum five years of related work experience in a highly regulated manufacturing environment.
  • BS degree in engineering or related field (plastics, mechanical, manufacturing, or materials preferred).
  • Experience specifying and procuring Injection Molding Tooling, Molding Machines, and Auxiliary Equipment.
  • Proficiency in project management software and MS Office.

Responsibilities

  • Establish project timelines and drive timely completion of projects.
  • Interface with customers, suppliers, and internal resources professionally.
  • Define and manage scope, time, budget, and resources of projects.
  • Coordinate DFM with engineers, vendors, customers, and project teams.
  • Lead validation to launch new products and molds, with documentation per standards.
  • Manage molding validation plans, protocols, reports, and metrology coordination.
  • Submit and approve change orders for new or revised processes.
  • Train production personnel on new and revised processes.
  • Create technical documents such as protocols and reports.

Skills

Project management
Verbal communication
Written communication
Team collaboration

Education

Bachelor's degree in Engineering

Tools

SolidWorks
MS Project
Smartsheet
Excel
PowerPoint

Job description

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.

WE ARE OPEN TO RELOCATING QUALIFIED CANDIDATES!

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.

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 or another highly regulated manufacturing environments with a 13485 ISO minimum ).
  • B.S. degree in an engineering or related field or equivalent experience (Plastics, mechanical, manufacturing, or materials preferred).
  • 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 Plastics, mechanical, manufacturing, silicone/LSR or materials preferred.
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