Jobs at Roche

Lead global clinical and companion diagnostic studies from design through close-out, managing timelines, budgets, CROs and cross-functional stakeholders. Ensure regulatory compliance, study documentation, publication of results, and audit/inspection readiness while delivering study objectives on time and within scope.

Provide QA oversight for regulated IT systems, develop and revise CSV and GxP standards, gather global feedback, support IT4IT system validation and M&A activities, escalate non-compliance, partner with stakeholders to define product roadmap and governance, manage product lifecycle, and lead quality and compliance discussions.

Manage key pathology accounts, drive sales of pathology portfolio, oversee analyzer deployments, provide application support and user training, manage public tender activities, collaborate with marketing, and maintain CRM records.

Hands-on role developing and optimizing novel NGS sequencing assays on the Axelios SBX platform. Lead experimental design, troubleshooting, and assay transfer to CLIA labs. Collaborate with commercial partners and bioinformatics to analyze data, document SOPs, mentor junior scientists, and drive strategic R&D initiatives to support pharma collaborations and diagnostic assay adoption.

Lead and operate the local Quality Management System for clinical and pharmacovigilance activities, ensure compliance with GCP/GVP and local regulations, manage audits/inspections, drive CAPA and continuous improvement, oversee external vendors, and establish local training and risk management frameworks.

Lead safety strategy and pharmacovigilance for complex molecules across the product lifecycle. Provide expert review for safety decisions, regulatory submissions (IND/NDA/MAA), risk management plans, and mentor colleagues. Influence cross-functional stakeholders, apply statistical analyses to safety data, and represent safety expertise to regulators and leadership to ensure patient safety and data reliability.

Lead strategy, design and delivery of internal executive events and experiences (town halls, hybrid forums, strategy sessions). Partner with senior leaders to craft narrative, agendas and engagement formats; provide technical oversight of platforms and installations; run global programmes with governance and stakeholder alignment; develop and certify team members; and drive cross-functional collaboration and innovation in employee engagement.

Lead global semiconductor category strategy, manage foundries/distributors, drive high-value negotiations, mitigate supply risks, build resilience and sustainability pipelines, develop procurement guidance, coach team members, and partner with senior stakeholders to align sourcing with business needs.

Owns product outcomes for digital pathology and imaging analytics, leading continuous discovery, cross-functional alignment, and data-driven decisions to deliver measurable business results. Provides strategic context, customer advocacy, risk ownership, and drives commercial and technical feasibility while enabling teams to deliver outcome-focused development.

Lead IHC functional screening and antibody development for rabbit monoclonals; develop, optimize, and validate IHC assays on FFPE samples; perform research testing and orthogonal confirmation (Western blot, ELISA, RNA ISH, IF); troubleshoot and improve antibody performance; provide scientific leadership and mentor junior staff; collaborate cross-functionally and contribute to publications, patents, and regulatory activities. Onsite in Pleasanton, CA.

Provide advanced technical support for Roche diagnostic systems: troubleshoot complex application issues, resolve customer inquiries, coordinate escalations via CRM, develop corrective action plans with field service, deliver basic customer training, and support sales with technical and lab layout guidance.

Lead technical development of combination products and drug delivery devices through design controls, testing, regulatory compliance, and cross-functional collaboration. Provide technical leadership, evaluate new technologies, oversee external partners, drive investigations and issue resolution, and author design control and risk documentation to ensure safe, robust, and compliant products.

Lead strategic workforce planning initiatives by partnering with business leaders and cross-functional teams to diagnose needs, define recommendations, and enable data-driven workforce strategies. Support SWP product enablement, training, and scaling (30%+ capacity) and advise on skills, AI/tech impacts, location strategies, and external workforce optimization. Drive stakeholder engagement, change management, and strategy execution across a global, matrixed HR environment.

Lead a cluster sales/operations team (20+), manage state P&L, build stakeholder relationships, shape market access, ensure compliance, implement strategic and operational plans, and drive KPIs and partnerships to increase access to Roche innovations.

Provide strategic legal and compliance counsel to commercial teams, manage contract drafting and negotiation, ensure adherence to healthcare regulations and industry codes, implement global compliance and privacy initiatives locally, maintain legal documentation and SOPs, and act as subject-matter expert on Indonesian healthcare and corporate law while supporting regional and global legal networks.

Perform day-to-day and month-end accounting activities including leased assets, fixed assets, CAPEX, taxes, GL journals, accruals/provisions, bank and customer clearing, AR invoicing, cost/revenue allocation, SAP MM product closing, reporting for consolidation, and audit documentation.

Lead technical development of drug-device combination products (pen/autoinjectors), provide SME guidance, author design control documentation, oversee design verification/validation and risk management, resolve complex device issues, ensure compliance with ISO 13485/14971 and 21 CFR Part 820, and collaborate cross-functionally and with external partners through product lifecycle to support clinical and commercial readiness.

Lead and oversee international quality systems and compliance across regions for Roche products. Drive implementation of quality management processes, coordinate audits and corrective actions, ensure regulatory compliance, and collaborate with cross-functional teams to maintain product quality and continuous improvement.

Provide legal advice across UK and Ireland commercial pharmaceutical matters, lead operational data protection (DSRs, privacy incidents), support R&D and clinical trial agreements, ensure compliance with ABPI and anti-bribery rules, maintain legal templates, and advise business stakeholders to mitigate legal and commercial risk.

Manage assigned territory and customer accounts to achieve sales targets. Develop new accounts, maintain strong customer relationships, resolve complaints, coordinate with distribution and professional service teams, and support the District Sales Manager as needed to ensure customer satisfaction and long-term partnerships.