Jobs at Johnson & Johnson

Provide Anaplan system support for FP&A users: investigate ServiceNow issues, act as SME for models, ensure data integrity between sources and Anaplan, prepare and execute test scripts for fixes/enhancements, collaborate with technical teams to implement improvements, and maintain documentation to improve user experience.

Lead production of plain-language summaries (PLS) for clinical trials, ensuring scientific integrity, regulatory compliance, vendor oversight and clear presentation of results for lay readers. Review drafts, apply health literacy and statistical principles, maintain SOPs/templates, coordinate cross-functional stakeholders, facilitate translation hand-offs, and drive process improvements and metrics.

Lead production of plain language summaries (PLSs) for clinical trials, ensuring scientific integrity, regulatory compliance, vendor oversight, cross-functional alignment, and clarity for lay readers. Develop scalable PLS processes, review drafts, resolve content issues, apply health literacy principles, and support hand-off for translation while tracking metrics and updating procedures.

Lead Ethicon India commercial operations including channel and TPI/dealer management, end-to-end tender pricing and documentation, secondary sales and incentives, compliance and audits, master data and MIS/dashboards, digital solutions implementation, customer service processes (PDC/PRIs), training, and analytics-driven process improvements to support sales and service objectives.

Support India Hospital MedTech FP&A by managing month‑end/quarter‑end close, budgeting, forecasting, variance analysis, reporting, dashboards, process improvements, and partner with business finance and global teams to deliver actionable financial insights.

Seeking a highly skilled analytical scientist to lead method development using Mass Spectrometry for pharmaceutical products and ensure compliance with regulatory standards.

The role involves managing a communications team, directing external communications operations, and developing strategic communications plans to enhance organizational excellence.

Lead local management of country-level clinical trials from start-up through database lock and closeout. Coordinate and mentor local trial teams, ensure GCP/SOP/regulatory compliance, manage site selection, budgets, vendor selection, CAPA, investigator meetings, reporting, and trial documentation. Serve as primary country contact and drive process improvements and training.

Provide broad legal counsel and mentorship for Innovative Medicine India, handling contracts, litigation management, regulatory and compliance advice, IP coordination, M&A due diligence, training, and cross‑functional legal support to enable compliant business growth.