Step into a pivotal role at a global medical device innovator where your work will directly impact patient outcomes and healthcare systems around the world. If youre looking to shape smarter safer and more efficient healthcare solutions this is where your expertise will shine.
Why You Should Apply
- Join a company whose products touch millions of lives globally
- Work on cuttingedge solutions that improve patient safety and care
- Be part of a collaborative innovationdriven team culture
- Excellent benefits including medical dental vision 401(k) with match tuition reimbursement and more
What Youll Be Doing
- Lead and implement quality improvements for products and manufacturing processes
- Drive root cause analysis CAPAs and quality engineering best practices
- Review and approve validation change control and qualification documents
- Investigate and resolve customer/internal complaints with technical rigor
- Develop test methods quality plans SOPs and inspection procedures
- Train team members in quality systems and regulatory compliance
About You
- Be able to do the job as described
- Comfortable developing and executing master validation and strategic quality plans
- Strong grasp of FDA and ISO compliance standards
- Certified Quality Engineer (CQE) Auditor (CQA) or Quality Manager (CQM) preferred
- Proficient in statistical analysis and experimental design
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.
Required Experience:
Senior IC