Quality Engineer - High Tech Medical Devices
Michael Page Streamwood
About Our Client
Our client is a medical device manufacturer located in the Streamwood area. They seek a Quality Engineer to join their ever-expanding Quality team. Their clients include well known OEMs, such as Stryker and Medtronic. This role will be responsible for customer communication, root cause/corrective actions and leading floor initiatives to increase efficiency.As mentioned, this organization is growing rapidly with an extremely innovative product line that's taking the Medical Device world by storm.
Job Description- Supports regulatory and agency inspections, audits, investigations, and inquiries regarding the control and assessment of product design and manufacturing quality.
- Leads and implements various product and process improvement methodologies.
- Review the adequacy and correctness of changes to Bill of Materials (BOM's), Assembly Procedures, Drawings, Component Specification, FMEAs, Control Plans, etc.
- Leads in the completion and maintenance of risk analysis.
- Leads generation and completion of protocols and reports for test method validations.
- Interfaces with Manufacturing Engineers to review processes for new and existing products and coordinate process validations and capability studies. Recommends process monitoring devices where applicable.
- Develops various inspection techniques and procedures to ensure product integrity to design specifications. Responsible for the writing, approval and implementation of Incoming, In-Process and Final Inspection procedures.
- Ensures that the disposition of non-conforming materials meet all necessary regulatory requirements and assure adequacy of corrective actions to prevent re-occurrence.
MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.
The Successful Applicant- Relevant Quality Assurance Engineering Experience
- Bachelor's Degree (Science Related)
- 3+ years of experience in a Cleanroom environment
- Strong Medical Device Manufacturing Experience
- Good knowledge of statistical tool sand appropriate use of Design of Experiments (DOE) when developing recommendations
- Excellent communication and interpersonal skills
- Working knowledge of FDA, EU MDR, ISO 13485:2015, 21 CFR and cGMPs
- Competitive base salary between $80,000-$95,000, depending on experience and skills
- Bonus opportunity up to 5%
- Comprehensive benefits package including Medical, Dental and Vision
- Life and AD&D Coverage
- Short-term disability coverage
- 15 PTO Days + 10 holidays
- 401(k) with 6% company match
Michael PageStreamwood
duties to junior engineers and technicians
• Work directly with customers to discuss reports and non-conformances
• Lead corrective actions through Root Cause Analysis methods
• Generate documentation and standards for new products
• Work...
RandstadElk Grove Village, 11 mi from Streamwood
job summary:
Growing manufacturer is seeking a direct-hire Quality Engineer. This position is located near Elk Grove Village, Illinois. The Quality Engineer will manage continuous improvement initiatives by monitoring key quality metrics, conducting...
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and enjoyment throughout the process.
Job Description
The Supplier Quality Engineer will be responsible for the following:
• Qualify and approve potential suppliers and components through activities such as Potential Supplier Audits (PSA), business case...