Principal Business Quality Analyst
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What you'll do
- Interact with client users and internal product owners to gather and author business, functional & non-functional requirements improvements for software products
- Running workshops and pilots with clients for product requirement and implementations
- Application installations, configurations and business process mappings for drug safety and pharmacovigilance clients
- Issue / bug prioritization & management in ticketing management system (JIRA)
- Formal system validation (OQs, PQs and IQs) and other SDLC documentation activities like authoring Test Strategy, Test Plan, Traceability Matrix, Test Summary Report, etc.
What they're looking for
- Bachelor’s degree from a good college like B.Tech., B.IT or similar
- 5-8 years of total experience in software industry with at least 3 years in business and functional requirements analysis and authoring experience in pharmacovigilance domain.
- Medium level knowledge of SQL
- Knowledge of Drug Safety (Pharmacovigilance) domain
- Knowledge of a leading Drug Safety System like Argus Safety, ArigG, etc.
- Experience of system validation in Pharmacovigilance or Drug Safety domain
- Self-driven personality, ability and interest to guide junior team members
- Demonstrated proficiency in working on multiple projects and deadlines
- Strong problem solving and troubleshooting skills
- Good communication, presentation and documentation skills
Nice to have
- Knowledge of periodic/aggregate reporting (PBRER, DSUR, PADER etc.)
- Business process mapping experience with clients
- Experience of working with enterprise software application
- Working knowledge and experience of Oracle Database, Agile/JIRA, Confluence
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
General Purpose: Business/functional/application consultant on client/internal project, leading software product business, functional & application requirement analysis and documentation, supporting business process development, configuration, implementation, testing & validation of software applications.
Essential Duties & Responsibilities:
• Interact with client users and internal product owners to gather and author business, functional & non-functional requirements improvements for software products
• Running workshops and pilots with clients for product requirement and implementations
• Application installations, configurations and business process mappings for drug safety and pharmacovigilance clients
• Issue / bug prioritization & management in ticketing management system (JIRA)
• Formal system validation (OQs, PQs and IQs) and other SDLC documentation activities like authoring Test Strategy, Test Plan, Traceability Matrix, Test Summary Report, etc.
Minimum Requirements:
• Bachelor’s degree from a good college like B.Tech., B.IT or similar
• 5-8 years of total experience in software industry with at least 3 years in business and functional requirements analysis and authoring experience in pharmacovigilance domain.
• Medium level knowledge of SQL
• Knowledge of Drug Safety (Pharmacovigilance) domain
• Knowledge of a leading Drug Safety System like Argus Safety, ArigG, etc.
• Experience of system validation in Pharmacovigilance or Drug Safety domain
• Self-driven personality, ability and interest to guide junior team members
• Demonstrated proficiency in working on multiple projects and deadlines
• Strong problem solving and troubleshooting skills
• Good communication, presentation and documentation skills
Preferred Qualifications:
• Knowledge of periodic/aggregate reporting (PBRER, DSUR, PADER etc.)
• Business process mapping experience with clients
• Experience of working with enterprise software application
• Working knowledge and experience of Oracle Database, Agile/JIRA, Confluence
Company
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