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Position Summary:

Job Title: Sr. Development Quality Engineer

Duration: 06 Months --Contract--Possible extension

Tax Term: W2

Position Summary:

The Sr. Development Quality Engineer will serve as a technical representative providing design quality expertise to a product development team. Responsible for maintaining a strong collaborative partnership with cross-functional team members to achieve patient/user safety, customer satisfaction, and organizational success.

RESPONSIBILITIES:

• Lead and/or support on-time completion of Design Control deliverables

• Support the establishment of objective, measurable, and verifiable product requirements

• Support Design Verification and Validation planning & execution, including any cross-functional investigation & resolution activities

• Lead Risk Management activities from product concept through commercialization

• Support test method development and lead test method validation activities

• Support manufacturing process development & qualification for new product and design changes

• Support the establishment of component specification definitions, supplied component sampling plan development, and vendor qualifications

• Support biocompatibility and sterilization qualifications

• Support audits and quality system improvement activities

• Support Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and regulatory requirements.

• Comply with Abbott, U.S. FDA, EUMDR and other requirements, as applicable.

• Maintain positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and suppliers.

Basic Qualifications:

• Bachelor’s degree in Engineering or Technical Field.

• Minimum of 5 years of experience in R&D, Process/Manufacturing Engineering, and/or Quality with at least 2 years supporting product development.

• Experience in medical devices and associated regulations/standards.

• Experience in test method development and validation

• Experience in preparing risk assessments, FMEA and other risk documents.

Preferred Qualifications:

• Advanced Degree in Engineering/Technical Field

• Experience in active implantable medical devices.

• Knowledge of requirements management tools (e.g., DOORS) and use of problem reporting systems (e.g., JIRA).

• Working knowledge of statistics and its application to verification and validation

About US Tech Solutions:

US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit www.ustechsolutions.com (http://www.ustechsolutionsinc.com/) .

US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.