Plastics Engineer

Integrated Resources, Inc ( IRI ); Indianapolis (IN); On-site; Full time

Job summary

A leading company in the manufacturing of medical devices is seeking a Plastics Engineer to lead projects in Indianapolis, IN. The position requires at least 5 years of experience in plastics tooling and a Bachelor's degree in a related field. The successful candidate will manage the design and development of products, ensuring compliance with industry standards and collaborating across teams.

Qualifications

• Minimum 5 years of experience in plastics tooling and manufacturing processes.
• Experience with data-driven analysis methods such as DOE and FMEA.
• Excellent technical writing and PC skills required (MS Office).

Responsibilities

• Lead and execute projects related to the design of plastic medical devices.
• Ensure all projects are completed on time, within budget, and meet quality standards.
• Collaborate with cross-functional teams to resolve technical issues.

Skills

Data-driven analysis

Problem-solving

Technical writing

Lean Manufacturing

Education

Bachelor's degree in Mechanical, Plastics or Manufacturing Engineering

Tools

SolidWorks

Minitab

Job description

20 hours ago Be among the first 25 applicants

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Integrated Resources, Inc ( IRI ) provided pay range

This range is provided by Integrated Resources, Inc ( IRI ). Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$50.00/hr - $51.00/hr

Direct message the job poster from Integrated Resources, Inc ( IRI )

Lead Recruiter at Integrated Resources Inc.(Scientific/ Clinical/Life Sciences /Pharmaceuticals /Engineering/Healthcare/ Business Professionals)

Location: Indianapolis, IN

Duration: 12+ months

Day shift, M-F

Top 3 must haves:

• Minimum 5 years of experience in plastics tooling and manufacturing processes.
• Bachelor's degree in mechanical, Plastics or Manufacturing Engineering.

Job Description:

• The Plastics Engineer –will be responsible for leading and executing projects related to the design and development of plastic medical devices, ensuring that the products meet quality, cost, and delivery requirements.
• This will involve working closely with cross-functional teams such as R&D, Manufacturing, Quality, and Supply Chain.

Qualifications:

• Minimum 5 years of experience in plastics tooling and manufacturing processes.
• Experience with data-driven analysis methods such as DOE, SPC, Mold Flow Analysis, and FMEA.
• Experience using CAD/CAE tools (SolidWorks preferred), GD&T, Minitab (or other statistical analysis software), and project management tools.
• Knowledge and experience in process development using Scientific Molding practices.
• Demonstrated technical leader with an ability to prioritize, focus efforts, overcome obstacles, and complete key objectives.
• Understanding validation requirements and processes applicable to the medical device industry.
• Experience with Lean Manufacturing tools.
• Excellent technical writing and PC skills required (MS Office) with attention to detail.
• Knowledge of critical material properties of polymers and how they influence the molding process and final product.
• Experience with the processing of polyolefin preferred.
• Lead and execute projects related to the design, development, and manufacturing of plastic medical devices.
• Ensure that all projects are completed on time, within budget, and to the required quality standards, with a focus on medical device industry requirements and validation processes.
• Provide technical guidance to project teams and collaborate with cross-functional teams to resolve technical issues.
• Develop and implement processes and tools to improve product quality and efficiency, with a focus on medical device industry requirements.
• Identify and evaluate new materials, technologies, and processes to improve product performance and competitiveness, with a focus on medical device industry requirements.
• Ensure that all design and development activities follow industry standards and regulations, including medical device industry requirements.
• Generate design change documents, perform risk analysis, and design transfer activities as needed.
• Participate in part and mold design reviews, troubleshoot, and resolve technical problems using problem-solving processes.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Science, Research, and Engineering

• Industries

  Pharmaceutical Manufacturing, Medical Equipment Manufacturing, and Biotechnology Research

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