Manual Testing (Pega/PlanView)
Jobsbridge1
Posted: May 28, 2015
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Quick Summary
We are seeking a skilled Manual Testing professional to join our team in Boston, MA, as a Manual Testing (Pega/PlanView) team member. The ideal candidate will have experience in Biopharma/Biotechnology/ Clinical Research Organization and be able to perform functional, regression, integration, conversion, and end-to-end testing. The successful candidate will be responsible for managing testing activities and providing input into requirements/specification/design.
Required Skills
Job Description
Jobsbridge
Dear Associate,
We have this following position open. Please respond if interested.
Title : Manual Testing (Pega/PlanView)
Location : Boston, MA
Duration : 6+ Months
1. Manual Testing team member to manage functional, Regression, Integration /interfaces, Conversion, Reports, End to End testing.
2. Proven track record to perform all aspects of Quality Assurance, such as planning QA activities, providing input into requirements / specification / design.
3. Experience in Biopharma / Biotechnology / Clinical Research Organization is a plus.
4. Experience with agile software practices and managing work across more than one project.
5. Experience with various SDLC processes and how various QA activities and quality-centered best practices fit into such product development lifecycles.
6. Experience in Agile and waterfall methodology preferred.
7. Good communication skills.
8. Minimum of 6-8 years of experience providing Software QA and Testing services.
9. Experience working with offshore teams.
10. Experience using PRPC developer portals and Rules Explorer
11. Trained on PegaRULES Process Commander (PRPC), including both Fundamentals as well as Bootcamp.
12. Experience using PRPC’s Clipboard for testing
13. Experience using PRPC’s Performance Analyzer (PAL) to take performance readings for subsequent performance analysis
14. Experience reviewing and verifying such PRPC rules as validation rules and service levels
15. Experience with Project View tool - preferred
15. Familiarity with FDA regulations such as 21 CFR Part 11 and GxP desirable.
16. Good knowledge of SQL is must.
17. Knowledge of HP Quality Center 10.x or higher version.
18. JIRA exposure is a plus.
Best Regards,
Mike Curtis
All your information will be kept confidential according to EEO guidelines.