ATR International
SUMMARY OF POSITION:
Within the Airways R&D sustaining engineering group, the sustaining engineer's primary responsibility will be to support Airways disposable medical devices currently on the market The sustaining engineer will research, test and validate components, materials and applications while sustaining current product designs This position is responsible for the design history files, determining test requirements, V&V testing and/or coordinating V&V testing, and design controls In addition to implementing moderate design changes that either enhance performance or address quality issues, the sustaining engineer supports/ performs complaint investigations, determines root cause failure modes and provides solutions for these product lines
Support implementation of eIFU's (Electronic IFU) Program.
ESSENTIAL FUNCTIONS:
1 Provides technical support for existing products by developing solutions for problems somewhat complex in nature and/or of moderate organizational impact with a high level of accountability, moderate level of authority and some supervisory oversight.
2 Works to maintain product performance and quality for existing products by leading and assisting with issues relating to CAPAs, customer complaints and manufacturing processes, such as:
• Failure investigation and root cause analysis
• CAPA resolution
• Regulatory compliance
• Product Design Verification and Design Validation (performs V&V testing as needed)
• Design changes
• Test methods and tooling design
• Process enhancement and improvement
3 Supports research on raw materials, components and assemblies for MoC compliance (Materials of Concern, RoHS, Prop65, etc), eIFU's (Electronic IFU) Program.
4 Follows strict adherence to policies and procedures associated with an FDA controlled environment.
5 Generates Engineering Change Orders to support product sustaining efforts.
DEPARTMENT SPECIFIC/NON-ESSENTIAL FUNCTIONS:
1 Prepares analysis reports for managers, project leaders or other personnel.
2 Presents progress status to management and teams, as required.
3 Develops and tracks work schedule and assignments.
4 Provides input to departmental planning and resource activities.
5 Other duties as assigned with or without accommodation.
• Perform Design verification testing in Laboratory environment. • Update Product Design documentations in moderated changes such as Design History files, V&V testing report and protocols, Product Requirement documents adhering to design controls. • Makes minor changes in systems and processes to address Quality issues.
Requirement:
MINIMUM REQUIREMENTS: Education: BSME or BSEE or equivalent with manufacturing/mechanical experience and product life cycles.
Experience: 0-2 years of experience working in a multifaceted environment with internal and external customers in a technical support role.
Preferred Skills/Qualifications: • Demonstrated experience and a proven track record of success in product support evidenced by lowered support costs and by a failure rate reduction • Experience with internal and outsourced sustaining development projects • Proven ability to partner cross functional organizations to successfully drive the business (relationship building skills is key - influencing - working through people) • Solid working knowledge of quality and regulatory requirements • Must be a strong communicator, verbal and written, across various levels of the organization as well as cross functionally • Must be an extensive multi-tasker, and problem solver with high energy levels and strong organizational abilities Must be organized and attentive to details. • Medical Device and clinical environment experience • Sustaining engineering MoC programs, product design and project management experience. • CAD - Solidworks proficiency (3d models and 2d drawings) • MS Teams proficiency • Good documentation practices
Skills/Competencies: Problem solving, priority setting, customer focus and driving for results Minimum 4 days in the office at Lafayette campus is required.
Top 3 technical skills that are required for the role: 1 Knowledge of Design Verification testing and its documentation. 2 Knowledge of Quality, Regulatory requirements, Proficiency in Excel & Word applications. 3 CAD - Solidworks
Education Required: Mechanical Engineer, Biomedical Engineer, Electrical Engineer. Years' Experience Required: 0-1
TECHNICAL SKILLS Must Have CAD - Solidworks proficiency (3d models and 2d drawings) Labeling Design Verification Testing Product Design Verification and Design Validation (performs V&V testing as needed) Test methods and tooling design
Nice To Have Electronic IFU implementation Failure investigation and root cause analysis Process enhancement and improvement Regulatory Compliance
Benefits:
Benefits Full-time employees (working an average of 30 hours or more) are eligible to select from different benefits packages Packages may include medical, dental, and vision benefits, a 401(k) retirement savings plan with employer match (available after 1 year of employment), commuter benefits, employee discount and referral programs, and life and supplemental income insurance Paid sick leave is provided in accordance with applicable state and local laws.
Compensation Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education, and experience, as well as the benefits package you select.
Work Authorization ATR International, Inc cannot sponsor work visas (H-1B, F-1 STEM OPT with I-983, or similar) Candidates must have valid U.S work authorization.
ATR International, Inc is an equal opportunity employer We celebrate diversity and are committed to creating an inclusive environment for all employees.
ESSENTIAL FUNCTIONS:
1 Provides technical support for existing products by developing solutions for problems somewhat complex in nature and/or of moderate organizational impact with a high level of accountability, moderate level of authority and some supervisory oversight.
2 Works to maintain product performance and quality for existing products by leading and assisting with issues relating to CAPAs, customer complaints and manufacturing processes, such as:
• Failure investigation and root cause analysis
• CAPA resolution
• Regulatory compliance
• Product Design Verification and Design Validation (performs V&V testing as needed)
• Design changes
• Test methods and tooling design
• Process enhancement and improvement
3 Supports research on raw materials, components and assemblies for MoC compliance (Materials of Concern, RoHS, Prop65, etc), eIFU's (Electronic IFU) Program.
4 Follows strict adherence to policies and procedures associated with an FDA controlled environment.
5 Generates Engineering Change Orders to support product sustaining efforts.
DEPARTMENT SPECIFIC/NON-ESSENTIAL FUNCTIONS:
1 Prepares analysis reports for managers, project leaders or other personnel.
2 Presents progress status to management and teams, as required.
3 Develops and tracks work schedule and assignments.
4 Provides input to departmental planning and resource activities.
5 Other duties as assigned with or without accommodation.
• Perform Design verification testing in Laboratory environment. • Update Product Design documentations in moderated changes such as Design History files, V&V testing report and protocols, Product Requirement documents adhering to design controls. • Makes minor changes in systems and processes to address Quality issues.
Requirement:
MINIMUM REQUIREMENTS: Education: BSME or BSEE or equivalent with manufacturing/mechanical experience and product life cycles.
Experience: 0-2 years of experience working in a multifaceted environment with internal and external customers in a technical support role.
Preferred Skills/Qualifications: • Demonstrated experience and a proven track record of success in product support evidenced by lowered support costs and by a failure rate reduction • Experience with internal and outsourced sustaining development projects • Proven ability to partner cross functional organizations to successfully drive the business (relationship building skills is key - influencing - working through people) • Solid working knowledge of quality and regulatory requirements • Must be a strong communicator, verbal and written, across various levels of the organization as well as cross functionally • Must be an extensive multi-tasker, and problem solver with high energy levels and strong organizational abilities Must be organized and attentive to details. • Medical Device and clinical environment experience • Sustaining engineering MoC programs, product design and project management experience. • CAD - Solidworks proficiency (3d models and 2d drawings) • MS Teams proficiency • Good documentation practices
Skills/Competencies: Problem solving, priority setting, customer focus and driving for results Minimum 4 days in the office at Lafayette campus is required.
Top 3 technical skills that are required for the role: 1 Knowledge of Design Verification testing and its documentation. 2 Knowledge of Quality, Regulatory requirements, Proficiency in Excel & Word applications. 3 CAD - Solidworks
Education Required: Mechanical Engineer, Biomedical Engineer, Electrical Engineer. Years' Experience Required: 0-1
TECHNICAL SKILLS Must Have CAD - Solidworks proficiency (3d models and 2d drawings) Labeling Design Verification Testing Product Design Verification and Design Validation (performs V&V testing as needed) Test methods and tooling design
Nice To Have Electronic IFU implementation Failure investigation and root cause analysis Process enhancement and improvement Regulatory Compliance
Benefits:
Benefits Full-time employees (working an average of 30 hours or more) are eligible to select from different benefits packages Packages may include medical, dental, and vision benefits, a 401(k) retirement savings plan with employer match (available after 1 year of employment), commuter benefits, employee discount and referral programs, and life and supplemental income insurance Paid sick leave is provided in accordance with applicable state and local laws.
Compensation Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education, and experience, as well as the benefits package you select.
Work Authorization ATR International, Inc cannot sponsor work visas (H-1B, F-1 STEM OPT with I-983, or similar) Candidates must have valid U.S work authorization.
ATR International, Inc is an equal opportunity employer We celebrate diversity and are committed to creating an inclusive environment for all employees.