Job Description
Title: Development Engineer I
Location: Warsaw, IN 46580
Duration: 12 Months
Duties:
Principal Duties and Responsibilities:
Skills:
Principal Duties and Responsibilities:
Education:
Location: Warsaw, IN 46580
Duration: 12 Months
Duties:
- You have a key support role with responsibility for new product design, development, and commercialization;and/or to maintain in the market innovative medical device products in order to further Client s mission and grow Client s market leadership position.
Principal Duties and Responsibilities:
- With oversight from supervisor and mentorship by senior peers:
- Stays current with and understands relevant arthroplasty product intended use, clinical procedures, and related regulations and standards
- Identifies user needs through engagement with product users (often Orthopedic Surgeons) and observation of similar device usage
- Translates targeted user needs into design requirements/inputs which satisfy unmet market needs to achieve business goals while also complying with global regulatory requirements and recognized external industry standards
- Creates product designs which fully address targeted user needs/requirements, and authors design rationale to document basis of all design features
- Prepares and reviews information for invention disclosures and patents
- Initiates, provides instruction for and coordinates with support from Client cross-functional team members in the production and inspection of product prototypes for preliminary evaluation;and final design verification, design validation and process validation
- Creates product production specifications which appropriately account for design for manufacturability (process capability) and inspection
- Identifies and documents critical to quality product features based on product intended use, design requirements, associated user risks and the design itself to ensure appropriate quality control inspection plans are generated
- Evaluates, verifies and validates product designs relative to design requirements and to reduce user risk in compliance with Client procedures and global regulatory requirements (includes completing tolerance stack-ups, benchtop testing and executing simulated operating room cadaveric product evaluations)
- Authors, presents and obtains cross-functional team member approval of design control and risk management documentation as part of the product development process in compliance with Client procedures and global regulatory requirements
- Supports Client Quality, Sourcing and Manufacturing teams with new product design transfer tasks for production of market release quantities
Skills:
- You have a key support role with responsibility for new product design, development, and commercialization;and/or to maintain in the market innovative medical device products in order to further Client s mission and grow Client s market leadership position.
Principal Duties and Responsibilities:
- With oversight from supervisor and mentorship by senior peers:
- Stays current with and understands relevant arthroplasty product intended use, clinical procedures, and related regulations and standards
- Identifies user needs through engagement with product users (often Orthopedic Surgeons) and observation of similar device usage
- Translates targeted user needs into design requirements/inputs which satisfy unmet market needs to achieve business goals while also complying with global regulatory requirements and recognized external industry standards
- Creates product designs which fully address targeted user needs/requirements, and authors design rationale to document basis of all design features
- Prepares and reviews information for invention disclosures and patents
- Initiates, provides instruction for and coordinates with support from Client cross-functional team members in the production and inspection of product prototypes for preliminary evaluation;and final design verification, design validation and process validation
- Creates product production specifications which appropriately account for design for manufacturability (process capability) and inspection
- Identifies and documents critical to quality product features based on product intended use, design requirements, associated user risks and the design itself to ensure appropriate quality control inspection plans are generated
- Evaluates, verifies and validates product designs relative to design requirements and to reduce user risk in compliance with Client procedures and global regulatory requirements (includes completing tolerance stack-ups, benchtop testing and executing simulated operating room cadaveric product evaluations)
- Authors, presents and obtains cross-functional team member approval of design control and risk management documentation as part of the product development process in compliance with Client procedures and global regulatory requirements
- Supports Client Quality, Sourcing and Manufacturing teams with new product design transfer tasks for production of market release quantities
Education:
- Minimum B.S. Degree from an ABET accredited school (or global equivalent) in one of the following engineering disciplines: Mechanical Engineering, Mechanical Engineering Technology, Biomedical Engineering, Bioengineering, Biomedical Engineering Technology, Bioengineering Technology, Aerospace Engineering or Aeronautical Engineering.
Numbers & Facts
| Location | Warsaw, IN |
| Industry | Staffing/Employment Agencies |
| Salary | $40 |
| Company Size | 2,000 to 2,499 employees |
| Year Founded | 2000 |
| Website | http://www.lancesoft.com/ |
About Company
We are a $125 Million, NMSDC-certified Minority & Woman owned Workforce Solutions Company headquartered in the DC metro area with presence across US with global presence - Canada, Mexico, India, UK, Malaysia, Indonasia, Hongkong, Singapore, UAE. We are specialized in providing Workforce Solutions, SOW project delivery, Engineering Solutions, Creative Services. We currently support 100+ Fortune companies globally and across multiple industry segments. We are currently supporting several massive programs across industry segment nationally/globally (Intel, Ally, AMD, QUALCOMM, Morgan Stanley, Kraft/ Mondelez, MNP, Amdocs, Dell, SanDisk, Medtronic, Becton Dickinson, GE, Lockheed Martin, UTC, L-3 Communications, Caterpillar, BMW, Mercedes Benz, National Grid, Dominion, Energy Future Holdings, PSEG, 3M, Fidelity, Aetna, Humana, Johnson & Johnson, Pfizer, Merck etc).
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender, identity, national origin, disability, or protected veteran status.
Skills
- ABET (Accreditation Board for Engineering and Technology)unmatched
- Aeronautical Engineeringunmatched
- Aerospace Engineeringunmatched
- Bioengineeringunmatched
- Biomedical Engineeringunmatched
- Cross-Functionalunmatched
- Customer Support/Serviceunmatched
- Design Documentunmatched
- Design Verificationunmatched
- Documentationunmatched
- Industry Standardsunmatched
- Invention Disclosuresunmatched
- Invention Reviewsunmatched
- Leadershipunmatched
- Manufacturingunmatched
- Manufacturing Designunmatched
- Market Shareunmatched
- Mechanical Engineeringunmatched
- Medical Equipmentunmatched
- Medical Productsunmatched
- Mentoringunmatched
- Needs Assessmentunmatched
- Orthopedic Surgeryunmatched
- Patentsunmatched
- Process Capabilityunmatched
- Process Validationunmatched
- Product Designunmatched
- Product Developmentunmatched
- Product Testingunmatched
- Production Specificationsunmatched
- Prototypingunmatched
- Quality Controlunmatched
- Regulationsunmatched
- Regulatory Requirementsunmatched
- Requirements Managementunmatched
- Resolve Customer Issuesunmatched
- Risk Managementunmatched
- Training/Teachingunmatched
- Validation Testingunmatched
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