Lead Tester Location: Andover, MA Duration: 6-12 months
Prior Experience with a Medical Device maker is highly desired Responsibilities: 1. Responsible for managing the development & execution of Design Control deliverables, including the following: a. Review SW requirements documentation b. Develop Test Strategies, including Test Platforms & Tools c. Develop Test Plans d. Develop Test Cases e. Develop Test Procedures (i.e. Test Scripts), including critical areas such as Algorithm, White Box testing, etc. f. Manage Traceability mapping of requirements to test cases to test cases & using Caliber a plus g. Execute Test Plans & Test Scripts h. Manage Defect Reports i. Generate Test Reports j. Support Risk Management activities (Patient Safety & Security) 2. Responsible for supervising SQE team 3. Responsible for acting as Project Team Lead managing complex projects a. 1-2 years minimum project management experience using MS Project 4. Responsible for Managing issues and interfacing with cross-functional R&D departments Candidate Profile: 1. Bachelors Degree in a technology oriented discipline, Computer Science Highly Desirable 2. 8 to 10 years experience in a software quality organization, Medical Device Industry Highly Desirable 3. 2-5 years Project Management experience using MS Project, including managing metrics such as Earned Value, Cost Variance, Resource Loading, etc. 4. Demonstrate the ability to develop complex test platforms/harnesses to test complex algorithms, including unit & integration testing 5. Familiarity with software test techniques, manual & automated, for complex Medical Devices, Class 3 Defibrillators or Equivalent Highly Desirable. 6. Ability to write test plans, test cases, test scripts. 7. Ability to execute test plans & test scripts 8. Ability to manage defects, (and using ClearQuest a plus) 9. Good communication and teamwork skills 10. Familiarity with Risk Based Testing methodologies 11. Experience with software quality processes & SDLC methodologies in a regulated FDA environment, 12. Demonstrated Knowledge of General Principles of Software Validation ins Highly Desirable. Thanks and Regards, Ram K Vutukuri Pyramid Consulting, Inc. Office: 678-279-7172*111 || Fax: 678-935-4466 E-Mail: ra...@pyramidci.com<mailto:ra...@pyramidci.com> || www.pyramidci.com<http://www.pyramidci.com/> || Yahoo IM: ramak77 CMMi Level 4 Certified Offshore center GMSDC- Supplier of the Year (Class IV) - 2008 Deloitte - Technology Fast 50 in Georgia - 2006, 2007 ABC - Georgia Fast 50 Pacesetters Award - 2005, 2006, 2007, 2008 --~--~---------~--~----~------------~-------~--~----~ You received this message because you are subscribed to the Google Groups "SAP BASIS" group. To post to this group, send email to SAP-BASIS@googlegroups.com To unsubscribe from this group, send email to sap-basis+unsubscr...@googlegroups.com For more options, visit this group at http://groups.google.com/group/SAP-BASIS -~----------~----~----~----~------~----~------~--~---
