Vacancy expired!
- Must have 5 years of experience in validated applications in the Pharmaceutical industry
- This is a documentation centric role with a focus on in-depth analysis, maintaining different version (based on FDA approvals), proof reading the templates/forms
- Must have 5 years of experience in eliciting and creating requirements specifications (User Stories, User Requirements, and Functional Specifications)
- Must have 5 yrs of experience in: Record, manipulate, and generate reports on requirements stored in the requirements management tool (example JIRA, Blueprint Requirements Center, Requisite Pro or similar)
- Must have 5 yrs of experience in defect triaging, tracking and timely closure of defects utilizing defect management tool (example HP ALM)
- Must have 5 yrs of experience in Agile methodology (backlog mgmt., support product owner in prioritization, support development and test teams through sprints, elaborate detailed User stories and Acceptance Criteria)
- Knowledge of PEGA and Salesforce applications
- Support projects and initiatives within the Global Risk Management business area
- Ensure that various appropriate SDLC documents are kept up to date and are available
- Ability to do analysis and create mock ups and process flow to review with business area effectively
- Outline requirement specifications with the use of standard templates for both use cases and detailed software
- Manage requirements and ensure they are stored in document management systems
- Monitor changes to baseline requirements with applicable change control processes and tools
- Perform relevant activities including documentation, training, and other work as directed by Client.
Vacancy expired!