Sunrise Systems, Inc.
Quality Engineer - Medical Devices
Sunrise Systems, Inc., Franklin Lakes, New Jersey, us, 07417
Direct message the job poster from Sunrise Systems, Inc.
Contract Duration: 12 Months contract (W2 only)
Location : Franklin Lakes, NJ (locals only)
Hybrid 4 days a week in office
Travel domestic
Role
The Quality Engineer is accountable for supporting new product development and product maintenance through the application of Quality Engineering skills for medical devices.
This person will handle projects and tasks, from product inception through product launch and maintenance, and play an active role in the process to ensure products meet quality standards consistent with both Corporate and Unit policies, while meeting all design control and other regulatory requirements.
Job Responsibilities
Consistent application of technical principles, theories, concepts, techniques, and quality sciences/tools.
Proven problem‑solving skills.
Makes measurable improvements to Client processes and procedures.
Ensures that all design control and production/process control projects meet applicable regulatory (local and international), Corporate, and Unit requirements.
Acts as a team member representing Quality on new product development and sustaining engineering projects.
Reviews and has Quality Engineering approval authority for new and modified design/process specifications including product performance specification, test methods, etc.
Assists with supplier and internal quality system audits as a means of evaluating the effectiveness of the established Quality System and good manufacturing practices (Auditor‑in‑training).
May perform other duties as required.
Education and Experience
Typically requires a minimum of a bachelor's degree in science, engineering, or other relevant discipline and a minimum of 5 years relevant experience or a combination of equivalent education and relevant experience.
Knowledge and Skills
Applied knowledge of the FDA medical device quality system regulations and international quality system standards/regulations (e.g. – 21 CFR Part 820, ISO 13485, ISO 14971, MDSAP, EU MDR/IVDR) as it relates to the design and continued support of Client products.
Applied knowledge of Corporate and/or Unit requirement.
Able to contribute to the completion of specific programs and projects.
Can ensure quality conduct of projects, including design, data summary and interpretation, and report generation for self and lower level project developers.
Able to revise policies and procedures.
Able to make presentations.
Can independently determine and develop approach to solutions.
Able to provide guidance and work direction to lower level project developers.
Can design and perform development working independently within defined parameters with minimal supervision required.
Experience with Client software systems utilized in the Quality Systems is desirable.
Must have knowledge/specialization in one or more of the following areas:
Acceptance sampling theory and application
Statistical process control methods and application
Measurement system/test method knowledge and analysis
Quality planning
Failure analysis investigation
Design of Experiments
Process mapping and value stream analysis
Hypothesis testing
Descriptive statistics
Process capability analysis
Basic quality tools: Pareto, box plots, histograms, scatter diagrams, etc.
Supplier quality management
Auditing
Design/development tools
Process validation
Software validation
Compensation: The hourly rate for this position is between $45-$48 per hour.
Benefits: Sunrise offers ACA compliant medical coverage/dental insurance/vision insurance to all employees. We also offer Sick time benefits as required per State regulations.
Seniority level Not Applicable
Employment type Contract
Job function Medical Equipment Manufacturing
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Contract Duration: 12 Months contract (W2 only)
Location : Franklin Lakes, NJ (locals only)
Hybrid 4 days a week in office
Travel domestic
Role
The Quality Engineer is accountable for supporting new product development and product maintenance through the application of Quality Engineering skills for medical devices.
This person will handle projects and tasks, from product inception through product launch and maintenance, and play an active role in the process to ensure products meet quality standards consistent with both Corporate and Unit policies, while meeting all design control and other regulatory requirements.
Job Responsibilities
Consistent application of technical principles, theories, concepts, techniques, and quality sciences/tools.
Proven problem‑solving skills.
Makes measurable improvements to Client processes and procedures.
Ensures that all design control and production/process control projects meet applicable regulatory (local and international), Corporate, and Unit requirements.
Acts as a team member representing Quality on new product development and sustaining engineering projects.
Reviews and has Quality Engineering approval authority for new and modified design/process specifications including product performance specification, test methods, etc.
Assists with supplier and internal quality system audits as a means of evaluating the effectiveness of the established Quality System and good manufacturing practices (Auditor‑in‑training).
May perform other duties as required.
Education and Experience
Typically requires a minimum of a bachelor's degree in science, engineering, or other relevant discipline and a minimum of 5 years relevant experience or a combination of equivalent education and relevant experience.
Knowledge and Skills
Applied knowledge of the FDA medical device quality system regulations and international quality system standards/regulations (e.g. – 21 CFR Part 820, ISO 13485, ISO 14971, MDSAP, EU MDR/IVDR) as it relates to the design and continued support of Client products.
Applied knowledge of Corporate and/or Unit requirement.
Able to contribute to the completion of specific programs and projects.
Can ensure quality conduct of projects, including design, data summary and interpretation, and report generation for self and lower level project developers.
Able to revise policies and procedures.
Able to make presentations.
Can independently determine and develop approach to solutions.
Able to provide guidance and work direction to lower level project developers.
Can design and perform development working independently within defined parameters with minimal supervision required.
Experience with Client software systems utilized in the Quality Systems is desirable.
Must have knowledge/specialization in one or more of the following areas:
Acceptance sampling theory and application
Statistical process control methods and application
Measurement system/test method knowledge and analysis
Quality planning
Failure analysis investigation
Design of Experiments
Process mapping and value stream analysis
Hypothesis testing
Descriptive statistics
Process capability analysis
Basic quality tools: Pareto, box plots, histograms, scatter diagrams, etc.
Supplier quality management
Auditing
Design/development tools
Process validation
Software validation
Compensation: The hourly rate for this position is between $45-$48 per hour.
Benefits: Sunrise offers ACA compliant medical coverage/dental insurance/vision insurance to all employees. We also offer Sick time benefits as required per State regulations.
Seniority level Not Applicable
Employment type Contract
Job function Medical Equipment Manufacturing
Referrals increase your chances of interviewing at Sunrise Systems, Inc. by 2x
Get notified about new Quality Engineer jobs in
Franklin Lakes, NJ .
#J-18808-Ljbffr