Maxine curry dayjob limited the big peg 120 vyse street birmingham b18 6nf england t.
Medical device testing resume.
Develop and implement technical qa protocols methods for pi and pm.
5 years of experience in leading complex software testing projects and other tester 5 years of web and test automation experience 2 years of experience in agile software development and testing.
100 broadway lane new parkland ca 91010.
Test lead engineer medical devices resume examples samples.
Successfully leading a team of 4 team members working on complex project where analysis of situations or data requires an in depth evaluation of multiple factors.
Houston tx 77028 555 555 5555 email job objective seeking work as a medical device quality engineer in which to exercise my past experience in the field for the good of the company.
Qa analyst sr.
Drive quality improvements initiatives and leadership within operations.
Lead qa tester software systems group 8 08 to 3 12 qa tester software solutions group 8 04 to 8 08 promoted to serve as lead qa tester overseeing quality assurance testing and teams for client software and systems development projects.
Improved sw product definition and development process by introducing agile review methods.
The most common activities listed on a test technician resume sample include handling workstations reviewing electronic reports collaborating with engineers making suggestions for product improvement and performing calibration tests.
Coordinating functional testing integration testing uat and regression testing.
Quality validation engineer medical devices vastek group inc san diego ca usa.
Troubleshot faults within test automated systems and connected devices.
A goal oriented and results driven sales professional who has a proven ability to influence the buying decisions of customer s.
Medical device sales resume.
0044 121 638 0026 e.
Maxine has the ability to create interest in.
Medical device test lead resume examples samples 8 10 years of experience in medical device product verification regulatory compliance risk management and sw hazard analysis activities for class i ii and class iii medical devices against fda qsr 820 iso 13485 aami tir 45 fda validation guidance and iec 62304 and gamp 5 computer system.