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Tier-1 employer and metro location increase applicants, but senior regulatory specialization limits competition.
Strong requirement for quality/regulatory and medical device knowledge reduces cross-industry transferability.
Explicit 7+ years, mandatory regulatory quality domain experience and specific tech stack enforce strict screening.
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Develop and deliver data solutions and dashboards for Quality and Regulatory Affairs (RAQA) stakeholders, ensuring data-driven decision support.
Extract and analyze data from enterprise data warehouse and various systems (SAP, CRM, Salesforce, TrackWise, Veeva) to uncover insights and automate reporting.
Own end-to-end project delivery including data solutions, ensuring compliance with global regulatory standards and providing audit support when required.
Bachelor’s or master’s degree with 7+ years of experience in data solutioning and dashboard reporting, preferably within quality and regulatory functions.
Proficiency in SQL, Python, and experience with BI tools (e.g., Snowflake) for data extraction, analysis, and visualization.
Experience working with enterprise applications such as SAP ECC, S/4 HANA, Salesforce, TrackWise, Veeva and extracting/analyzing system and logs data.
Work Location: Bengaluru, KA, India; Not Remote; Flexible working hours including occasional off-hours work due to business needs.
Experienced in quality management systems (QMS) and global regulatory compliance within medical device, pharmaceutical, or related industries.
Proven ability to independently manage multiple complex projects in a fast-paced, cross-functional environment with strong organizational discipline.
Familiarity with AI/ML concepts applied to data analysis and ability to transform query solutions into sustainable self-service reporting tools.