Careers

Manufacturing Engineer II

Job Title
Manufacturing Engineer II
Job ID
27385670
Location
Athens,  TX 75751
Other Location
Description

Manufacturing Engineer II, Athens TX.

We’re hiring for a Manufacturing Engineer II to join our Engineering Department at our Athens, TX facility.

Job Description: The Manufacturing Engineer will be responsible for leading and participating in creating, finding, and evaluating more efficient ways to manufacture products. This individual will work to develop and implement process validation protocols and reports for manufacturing processes and equipment, including IQ/OQ/PQ’s. This role will provide engineering support for sustaining the manufacture of medical devices at the Athens Texas facility.

This Manufacturing Engineer will work to troubleshoot and adjust processes to maintain quality and maximize product output; this will include performing ad-hoc problem-solving to develop corrective actions for customer issues or to initiate continuous improvements. This individual must have strong experience in process development with a background in validation and material qualifications. The ideal candidate will have a working knowledge of validation requirements, manufacturing methods, procedures, cost reduction, and yield improvement techniques. A background in material qualifications is preferred.

Manufacturing Engineer II Education and Experience Requirements:

  • Bachelor’s Degree or higher in material science, biomedical, mechanical, or industrial engineering.
  • Minimum of 2-5 years related experience in FDA/GMP regulated industry. Background in medical device assembly, materials, processes, and validation activities is preferred.
  • Proficient in AutoCAD, SolidWorks, Minitab, Word, Excel, and Project.
  • Experience in product production planning and working knowledge of manufacturing methods, procedures, and cost reduction/yield improvement techniques.
  • Experience in the application of statistical techniques such as statistical process control, design of experiments, and problem-solving techniques is required.
  • Experience with design, review, execution, and approval of Installation, Operation and Process Qualification protocols, and reports (IQ/OQ/PQ) required.

The Manufacturing Engineer will be responsible for estimating production times, staffing requirements, and related costs to provide information for management decisions. This engineer will work to analyze and plan workforce utilization, space requirements, workflow, and design layout of equipment and workspace for maximum efficiency. This individual will perform root cause analysis of product/process issues and implement short and long-term corrective actions to improve product quality and reliability. This role will confer with vendors to purchase equipment, materials, or parts and evaluate products according to specifications and quality standards. This role will require supplier qualifications and validation of new materials to be used in the existing product offering.

Argon Medical is a global manufacturer of specialty medical products, including a broad line of medical devices for Interventional Radiology, Vascular Surgery, Interventional Cardiology, and Oncology. With over 800 employees worldwide. Argon has manufacturing facilities located in Athens, TX, Wheeling, IL, and Rochester, NY. Argon’s brand is recognized for best-in-class products that improve patient outcomes via percutaneous, image-guided procedures. https://www.argonmedical.com/about/our-company

 If you are interested in hearing more about this Manufacturing Engineer II, contact a recruiter today at Andrew.Foran@argonmedical.com or apply online www.argonmedicaljobs.com

No third parties accepted for work on this role. Do not contact with unsolicited services or offers.

Required Skills

Bachelor’s Degree or higher in material science, biomedical, mechanical, or industrial engineering.
2+ years of thermoplastic injection/press molding experience required
Minimum of five (5) years related experience in FDA/GMP regulated industry. Background in medical device assembly, automation, and vision system technology preferred.
Proficient in AutoCAD, SolidWorks, Minitab, Word, Excel, and Project.
Experience in product production planning and working knowledge of manufacturing methods, procedures, and cost reduction/yield improvement techniques.
Experience in the application of statistical techniques such as statistical process control, design of experiments, and problem-solving techniques is required.
Experience with design, review, execution, and approval of Installation, Operation and Process Qualification protocols, and reports (IQ/OQ/PQ).

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