Job Description
Our Client, a Medical Device and Healthcare company, is looking for an Engineer Senior Manufacturing for their Madison, WI location.
Responsibilities:
Requirements:
Why Should You Apply?
Responsibilities:
- Support internal automation machines using Allen Bradley controls. Make software updates to support troubleshooting, improvement projects, and quality improvements.
- Integrate machine software with cloud networking for Process Monitoring, dashboard creation and tracking metrics.
- Lead or support new product introductions, design transfers, and product changes.
- Create documentation records per regulatory and quality requirements.
- Develop processes and procedures for new equipment.
- Apply defined procedures to execute and document changes to existing equipment.
- Identify, create, document, and execute protocols to support process or part changes.
- Define improvement opportunities, investigate issues, gather facts, analyze data, and draw accurate data-driven conclusions.
- Troubleshoot and repair equipment.
- Lead failure analysis investigations, identify root cause analysis, and develop solutions to resolve quality issues in a timely manner.
- Lead or support product non-conforming material reports, corrective and preventative actions, investigations, audits, or complaints. Document in accordance with applicable regulatory requirements.
- Provide subject matter expertise for custom equipment and processes.
- Lead or support new product introductions, design transfers, and product changes.
- Create documentation records per regulatory and quality requirements.
- Lead continuous improvement projects.
- Support the building and testing of custom equipment.
- Provide manufacturing support for the repair center.
- Identify opportunities, analyze data, and work with cross functional teams to implement solutions that improve production quality, capability, reliability, or reduce costs.
- Develop project plans, delegate effectively, and execute assigned tasks.
- Prioritize assignments and work independently with minimal guidance from leadership.
- Provide clear and concise documentation and communication of project needs, scope, budget, and status to peers and leadership.
- Follow procedures and maintain detailed records in accordance with FDA, ISO, CAP, CLIA requirements.
- Ability to work independently and as part of a team within a matrix organization.
- Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork.
- Support and comply with the company’s Quality Management System policies and procedures.
- Regular and reliable attendance.
Requirements:
- Ability to work designated schedule.
- Ability to lift up to 50 pounds for 5% of a typical working day.
- Ability to work in front of a computer screen and/or perform typing for approximately 80% of a typical working day.
- Ability to comply with all applicable personal protective equipment requirements.
- Ability to travel between Exact Sciences sites located in Madison, WI.
- Other duties as assigned.
- Minimum Qualifications:
- Bachelor’s degree in Engineering with 5+ years of experience; or, in lieu of Bachelor's degree, Associates degree in Engineering, Technology, Electronics, or similar field with 7+ years of experience.
- Effectively applies Engineering skills to complete assignments.
- Demonstrated ability to identify opportunities for improvement, clearly define project scope, and complete projects on time and on budget.
- Demonstrated ability to plan projects, balance multiple competing priority projects, and drove projects to successful completion.
- Preferred Qualifications
- 5+ years of experience in engineering or relevant life sciences / medical device industry.
- 5+ years of experience working in manufacturing or engineering environments applying problem solving skills (e.g., Six Sigma, probability and statistics) and process improvement (e.g. Lean).
- 5+ years of experience working in an FDA/cGMP/CAP/CLIA regulated production environment.
- 5+ years of experience working with Electronic Quality Management Systems and Manufacturing Software Systems.
- 2+ years of experience managing projects.
Why Should You Apply?
- Health Benefits
- Referral Program
- Excellent growth and advancement opportunities
Numbers & Facts
| Location | Madison, WI |
| Industry | Management Consulting Services |
| Salary | $42.44–$45.72 Per Hour |
| Company Size | 2,000 to 2,499 employees |
| Year Founded | 2000 |
| Website | https://www.iconma.com/ |
Benefits
401K, Employee Referral Program, Life Insurance
About Company
ICONMA is a global information consulting management firm providing Professional Staffing Services and Project-Based Solutions for organizations in a broad range of industries.
- Corporate Headquarters in Troy, Michigan; 20+ locations worldwide.
- Certified Woman-Owned Business Enterprise (WBE); certified by Women’s Business Enterprise National Council, National Women Business Owners Corporation (NWBOC); and California Public Utilities Commission (CPUC).
- Founded in 2000
- 2000+ Employees
The company was founded on the principle that success is derived from delivering high quality service and resources in the most responsive, flexible, and innovative way. ICONMA invests in people and resources with a single goal: To provide our customers with the highest quality service in the most responsive manner. Through its network of offices, ICONMA provides the resources to help clients maintain their competitive advantage.
Skills
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