Jobs at Johnson & Johnson

Promote pharmaceutical products for psoriasis and psoriatic arthritis across South London. Develop account plans, build relationships with dermatology and rheumatology healthcare professionals and key opinion leaders, deliver product presentations, achieve sales targets, analyze market and competitor trends, collaborate cross-functionally, support customers, and maintain accurate CRM records.

Leads regional deployment, integration, cutover, go-live, hypercare, and stabilization for SAP Finance and related transformation platforms. Governs readiness, risks, dependencies, controls, data, training, and support models while coordinating Finance, Supply Chain, Commercial, HR, external systems, global teams, and system integrators. Partners with business and technology leaders to drive adoption and value realization, and co-leads a globally distributed finance technology deployment team.

Supports global pharmaceutical regulatory submissions and health authority interactions, including INDs, CTAs, NDAs, MAAs, BLAs, and eCTD packages. Advises teams on regulatory requirements, submission strategies, protocols, labeling, and critical-path milestones. Coordinates country-specific filings, agency meetings, responses, inspections, audits, and lifecycle management. Partners with regulatory and cross-functional teams on strategy, competitive intelligence, process improvement, and project planning. Requires strong collaboration, organization, strategic thinking, and regulatory expertise.

Leads enterprise regulatory compliance across pharmaceutical and medical device businesses. Provides independent assessments of manufacturing, quality, inspection, audit, recall, and compliance risks; interprets regulations; supports inspection readiness and FDA responses; analyzes compliance data for executive insights; governs escalations; contributes to audits and acquisitions; and trains teams on risk-based cGMP auditing.

Designs, develops, verifies, and documents statistical programs for clinical data analysis and reporting. Performs quality control, maintains programming documentation, supports medium-to-high complexity tasks with minimal guidance, collaborates cross-functionally, ensures compliance with processes, and contributes to process improvement.

Develops and reviews clinical trial programming deliverables including CDISC SDTM submission packages, data model specifications, mappings, edit checks, listings and study-specific reports. Aggregates and transforms clinical data sources, performs quality control and verification, and supports process, system and tool improvements to ensure compliance and fit-for-purpose reporting to monitor safety, risk and regulatory requirements.