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Manufacturing Execution System (MES) Quality Engineer II

Jacobs Management Group
Elkton, MD Full Time
POSTED ON 4/15/2025
AVAILABLE BEFORE 5/6/2025

Job Description

Job Description

Are you passionate about optimizing manufacturing systems and ensuring quality compliance in a fast-paced, regulated environment? My client, a leading medical device company, is seeking an MES Quality Engineer II to drive continuous improvement and support the implementation of Manufacturing Execution Systems (MES). This is your chance to be a key player in a global organization that impacts patient care worldwide.

Why You Should Apply

  • Be a crucial part of a team ensuring seamless MES deployments and optimizations.
  • Work in a cutting-edge medical device manufacturing environment.
  • Opportunity to lead validation efforts and maintain compliance in a regulated industry
  • Comprehensive benefits : 401(k) match, health / dental / vision, paid time off, parental leave, tuition reimbursement, and more .

What You'll Be Doing

  • Support MES deployments, upgrades, and optimizations to improve manufacturing processes.
  • Maintain compliance of MES systems and integrity of the electronic device history record (eDHR) .
  • Develop and revise MES documentation, procedures, and validation test cases.
  • Collaborate with IT, Operations, and Engineering to enhance system functionality.
  • Train employees on MES processes and best practices.
  • About You

  • Be able to do the job as described.
  • Strong knowledge of 21 CFR 820, ISO 13485, and FDA medical device regulations .
  • Experience with Computer System Validation (CSV) and Change Management .
  • Familiarity with MES implementation and maintenance in a regulated setting.
  • Excellent problem-solving and communication skills.
  • How To Apply

    We'd love to see your resume, but we don't need it to have a conversation. Send an email to ccupo@jacobsmgt.com and tell me why you're interested. Or, if you do have a resume ready, apply here.

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