Software Quality Engineer job in Atlanta
Vacancy has expired
Atlanta CorTech LLC
| Job Ref: | 345838 |
| Employer: |
CorTech LLC |
| Job Type: | Contract |
| Salary and Benefits: | 51.72/Per Hour |
| Remote: | No |
Location |
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| City: | Atlanta |
| Post Code: | 30319 |
| Map: |
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Description |
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CorTech is seeking to hire a Software Quality Engineer for our client in Burlington, MA! Benefits Available! Weekly Pay! $51.72/Hour 8 AM - 5 PM This position is responsible for executing and maintaining quality engineering methodologies and providing quality engineering support for software utilized by the Client. Qualifications: -IEC 62304 exp required. -BS Degree in Engineering or Technical Field or equivalent experience. -2-5 years of Software Quality Engineering experience. -Detailed knowledge of FDA, GMP, IEEE 1012, and ISO 13485. -Advanced computer skills, including statistical/data analysis and report writing. Advanced Information Technology and data mining skills. -Prior medical device experience required. -ASQ CSQE certification desired. -Experience working in a broader enterprise/cross-division business unit model preferred. -Ability to work in a highly matrixed and geographically diverse business environment. -Ability to work within a team and as an individual contributor in a fast-paced, changing environment. -Ability to leverage and/or engage others to accomplish projects. - Strong verbal and written communication with the ability to effectively communicate at multiple levels in the organization. -Multitask and meet deadlines in a timely manner. -Strong organizational and follow-up skills, as well as attention to detail. -Ability to travel including internationally. Ability to maintain regular and predictable attendance. Duties: -Develop and conduct training of company personnel for the divisional software development and validation program. -Work with Design and Manufacturing Engineering in the completion of system/software requirements and other verification and validation processes. -Create and execute or direct software validation protocols traceable to system/software requirements. -Implement solutions for controlling code and administering Code Control and Software Event/Defect Tracking software systems. -Assist in the completion and maintenance of risk analysis, focused on software-related risks. -Design and implement various product and process improvement methodologies (i.e, Six Sigma and Lean Manufacturing). - Apply sound, systematic problem solving methodologies in identifying, prioritizing, communicating and resolving issues. -Software scoping and Part 11 audits. -Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements. -Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. -Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors. -Performs other related duties and responsibilities, on occasion, as assigned. | |
ref: (345838)
1040 days ago
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