Manufacturing System MES Quality Engineer II
Manufacturing System MES Quality Engineer II
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Salary Not Disclosed
1 Vacancy
Job Description
Are you passionate about optimizing manufacturing systems and ensuring quality compliance in a fastpaced 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 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 cuttingedge 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 Youll 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 problemsolving and communication skills.
How To Apply
Wed love to see your resume but we dont need it to have a conversation. Send an email to and tell me why youre interested. Or if you do have a resume ready apply here.
Employment Type
Full Time
