Junior Engineer
Our client is currently seeking a Junior Engineer.
Support the development and introduction of new orthopedic products and processes.
Work extensively with Product Development, Quality, Operations, Sterility and Packaging to take a product from design concept through production ramp up.
- Participate in multi functional teams, led by a Project Manager and be responsible for defined project deliverables - Manage Engineering Change Notices for new products from creation to final approval - Operate within quality system to produce documentation such as process validations, equipment qualifications, dynamic control plans, inspection plans and standard operating procedures - Operate within 'New Product Development Process' NPDP , to build robust processes through involvement in 'Design for Manufacturability' and 'Lean Manufacturing' initiatives - Utilize Six Sigma process tools such as 'Define, Measure, Analyze, Improve, Control' (DMAIC), 'Failure Modes & Effects Analysis' (FMEA), 'Design of Experiments' (DOE), Gage Repeatability & Reproducibility' (Gage R&R), 'Statistical Process Control' (SPC), capability analysis as required - Provide input to Capital Equipment Requests (CERs) -Create and execute equipment validation protocols for Factory Acceptance Testing, Supplier Acceptance Testing, and Equipment Qualifications as required -Create and execute Process Qualification protocols as required.
Qualifications and Work Experience Required:
- 2
years of engineering experience in the Medical Device, or similar, quality regulated industries - Demonstrated fundamental understanding of manufacturing processes, e.
g.
casting, forging, CNC machining, coating, etc.
- Demonstrated familiarity with theory and practical application of 'Geometric Dimensioning & Tolerancing' (GD&T) - Demonstrated experience with a parametric CAD design package, with a strong preference for ProE.
Should be capable of developing 2D drawings, manipulating 3D product models and modeling moderately complex fixtures and gages - Demonstrated proficiency in Microsoft Outlook, Microsoft Project, Microsoft Visio and Microsoft Office applications - Demonstrated interpersonal, communication and presentation skills.
Must be comfortable presenting at department level meetings - Demonstrated experience dealing with suppliers and resolving supplier issues, particularly for Supplier Innovation role - Must be challenged by a team-based environment which places a high degree of emphasis on accountability for customer satisfaction, cost reduction and quality/GMP compliance Education and Special Training Required:
Bachelors degree in a science, preferably Mechanical or Biomedical Engineering ID:
583624 Type:
Contract Salary:
Open.
Estimated Salary: $20 to $28 per hour based on qualifications.
Support the development and introduction of new orthopedic products and processes.
Work extensively with Product Development, Quality, Operations, Sterility and Packaging to take a product from design concept through production ramp up.
- Participate in multi functional teams, led by a Project Manager and be responsible for defined project deliverables - Manage Engineering Change Notices for new products from creation to final approval - Operate within quality system to produce documentation such as process validations, equipment qualifications, dynamic control plans, inspection plans and standard operating procedures - Operate within 'New Product Development Process' NPDP , to build robust processes through involvement in 'Design for Manufacturability' and 'Lean Manufacturing' initiatives - Utilize Six Sigma process tools such as 'Define, Measure, Analyze, Improve, Control' (DMAIC), 'Failure Modes & Effects Analysis' (FMEA), 'Design of Experiments' (DOE), Gage Repeatability & Reproducibility' (Gage R&R), 'Statistical Process Control' (SPC), capability analysis as required - Provide input to Capital Equipment Requests (CERs) -Create and execute equipment validation protocols for Factory Acceptance Testing, Supplier Acceptance Testing, and Equipment Qualifications as required -Create and execute Process Qualification protocols as required.
Qualifications and Work Experience Required:
- 2
years of engineering experience in the Medical Device, or similar, quality regulated industries - Demonstrated fundamental understanding of manufacturing processes, e.
g.
casting, forging, CNC machining, coating, etc.
- Demonstrated familiarity with theory and practical application of 'Geometric Dimensioning & Tolerancing' (GD&T) - Demonstrated experience with a parametric CAD design package, with a strong preference for ProE.
Should be capable of developing 2D drawings, manipulating 3D product models and modeling moderately complex fixtures and gages - Demonstrated proficiency in Microsoft Outlook, Microsoft Project, Microsoft Visio and Microsoft Office applications - Demonstrated interpersonal, communication and presentation skills.
Must be comfortable presenting at department level meetings - Demonstrated experience dealing with suppliers and resolving supplier issues, particularly for Supplier Innovation role - Must be challenged by a team-based environment which places a high degree of emphasis on accountability for customer satisfaction, cost reduction and quality/GMP compliance Education and Special Training Required:
Bachelors degree in a science, preferably Mechanical or Biomedical Engineering ID:
583624 Type:
Contract Salary:
Open.
Estimated Salary: $20 to $28 per hour based on qualifications.
|
|
 | |
