Lead all types of software product testing & validation activities
Lead the testing / validation team for internal software development process
Essential Duties & Responsibilities:
Interact with internal product owners and client users to understand business, functional & non-functional requirements, or improvements for software product.
Author and/or review validation test plan, strategy, requirement traceability matrix, validation test summary report for product releases based on project / product requirements.
Lead, mentor & guide the testing team members for all type of testing activities and artifacts including (but not limited to) system testing, functional testing, manual testing, automation testing, OQ, PQ, IQ etc.
Accountable for quality of testing and release of all product features and product validation documents / artefacts with high quality.
Exposure to Agile scrum structure and project tracking tools like Atlassian JIRA
Support and liaise with internal QA team for internal and external audits for product / project documents and artifacts.
Bachelor’s/Masters degree from a good college like B.Tech., MCA, etc.
7-10 years of total experience in software industry in all kinds of testing activities and SDLC
documentation with at least 2-3 years in life sciences domain.
At least 2-3 years’ experience of leading high performing testing teams of 4-8 members.
Well-organized and detailed oriented professional, with strong communication and highquality documentation skills
Self- motivated with ability to handle, organize and prioritize multiple tasks in a dynamic
high-volume work environment.
Analytical and process-oriented mindset
Good knowledge of Drug Safety (Pharmacovigilance) domain
Knowledge of a leading Drug Safety System like Argus Safety, ArisG, etc.
Led the testing / validation team and activities for external client implementation projects
Client facing experience
Experience of working with enterprise software application
Working knowledge and experience of Oracle Database, Agile/JIRA, Confluence
Knowledge of 21 CFR Part 11, EU Annex 11, GAMP5, GxP and CSV guidelines that are applicable to life sciences industry
Audit experience in supporting IT related systems/Client Interactions