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Manufacturing Engineer

JBL Resources

Arlington, TN

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JOB DETAILS
SALARY
$53
SKILLS
Communication Skills, Compiler Technology, Cross-Functional, Documentation, FDA (Food and Drug Administration), Human Resources, ISO (International Organization for Standardization), Logistics, Maintain Compliance, Manufacturing, Manufacturing Engineering, Manufacturing Operations, Manufacturing/Industrial Processes, Medical Equipment, Orthopedics, Problem Solving Skills, Process Development, Process Failure Mode and Effects Analysis (PFMEA), Process Flow, Process Validation, Quality Metrics, Regulations, Regulatory Compliance, Regulatory Requirements, Reporting Skills, Risk Management, Supply Chain Management, Supply Chain Operations, Technical Writing, Validation Documentation
LOCATION
Arlington, TN
POSTED
30+ days ago
Manufacturing Engineer
Location: Arlington, Tennessee
About Our Client:
Accepting no less than the absolute best, our client has climbed to the top, gaining a reputation for both excellence and satisfaction. Working at this company will give you the opportunity to work with some of the top technical professionals in the industry who are bringing cutting-edge products to forefront.  Offering results-driven people a place where they can truly make a difference on a daily basis, this is an opportunity you will not want to miss!
Key Responsibilities:
  • Supporting the EU MDR compliance project by compiling comprehensive technical documentation.
  • Developing manufacturing process flows to ensure regulatory adherence.
  • Conducting PFMEAs to identify and mitigate process risks.
  • Preparing validation reports to verify manufacturing processes meet standards.
  • Collaborating with cross-functional teams to ensure all documentation aligns with regulatory requirements.
Qualifications:
  • Familiarity with surgical solutions, biologics, and orthopedics manufacturing.
  • Previous experience supporting EU MDR compliance projects.
  • Knowledge of regulatory audits and readiness.
  • Relevant experience in medical device manufacturing, process validation, or related fields.
  • Prior experience in manufacturing operations within a regulated environment.
  • Strong knowledge of manufacturing processes, process flows, PFMEA, validation, and technical documentation specific to medical devices.
  • Ability to develop, review, and validate manufacturing procedures under stringent quality standards.
  • Experience supporting compliance with EU Medical Device Regulation (EU MDR), FDA, ISO, and other regulatory frameworks.
  • Excellent problem-solving skills, judgment, and the capacity to work independently with minimal supervision.
  • Effective communication skills for documenting technical processes and collaborating with cross-functional teams.
  • NO C2C CANDIDATES

Interested Candidates please apply on our website at https://jobs.jblresources.com.
For more information about our services and great opportunities at JBL Resources, please visit our website: https://www.jblresources.com.
JBL Resources is proud to have earned the reputation of being a premier provider of top talent professionals in the fields of engineering, human resources, logistics, operations, and supply chain management. As specialists in both permanent placement and contract services, our mission is to help companies and individuals become all they were created to be.
**JBL is an Equal Opportunity Employer and E-Verify Company
 

About the Company

J

JBL Resources