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Johnson & Johnson

Associate Director, Process – Digital

Johnson & Johnson

. Support Clinical Risk Management Operational Excellence by coordinating process optimization and day-to-day administration of the CRM digital landscape .

Posted 10/23/2026full-timeZug • SwitzerlandSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in Clinical Risk Management, focusing on process optimization, digital operations, and stakeholder coordination. Proficient in managing vendor relationships, audit readiness, and quality systems within regulated environments.

Highest-signal resume keywords
Process ImprovementDigital OperationsAudit ReadinessStakeholder CoordinationQuality Systems

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Process OptimizationDocument AdministrationChange ManagementData ManagementMetadata ConceptsQuality SystemsControlled DocumentationRoot-Cause AnalysisWorkflow CoordinationAction Plan Monitoring
Soft Skills
Strong OrganizationFacilitationCommunicationProblem-SolvingAttention to Detail
Tools & Technologies
Microsoft OfficeCollaboration PlatformsReporting ToolsBusiness Workflow ToolsTicketing Tools
Industry Keywords
PharmaceuticalMedical DeviceHealthcareRegulated EnvironmentGxPR&D QualityCommunities of PracticeSuper-User Networks

About the role

Key responsibilities & impact
  • Support Clinical Risk Management Operational Excellence by coordinating process optimization and day-to-day administration of the CRM digital landscape
  • Enable consistent operation, user engagement, controlled change, vendor delivery, and audit or inspection readiness across CRM tools and related services
  • Translate approved strategy and governance direction into operating routines, documentation, communications, reporting, and follow-through
  • Serve as operational point of contact for CRM super-user forums, vendor coordination, digital asset administration, taxonomy and metadata stewardship, portal support, governance logistics, escalation intake, and evidence coordination
  • Map current-state activities and identify administrative and workflow inefficiencies
  • Facilitate root-cause analysis, coordinate approved improvements, maintain action plans, and monitor adoption and effectiveness
  • Coordinate administration for CRM-owned tools and services, maintain support routines and user guidance, triage business questions, route technical issues, and support release readiness and communications
  • Plan and facilitate super-user forums, maintain agendas and decision or action logs, gather feedback, coordinate demonstrations and learning materials, and support adoption of approved changes
  • Coordinate vendor and service-provider deliverables, meetings, access, documentation, invoices or forecasts, risks, issues, and escalations
  • Coordinate audit and inspection evidence collection, organization, quality review, readiness materials, requests, and actions
  • Administer governance calendars, intake and escalation logs, decision records, CRM portal content, taxonomy, metadata, naming conventions, and controlled content organization
  • Compile operational measures, service trends, adoption feedback, action status, and improvement outcomes for leadership and governance forums

Requirements

What you’ll need
  • A minimum of a Bachelor's or equivalent University degree is required
  • Focus in life sciences, quality, technology, data, engineering, business, or a related discipline preferred
  • Relevant experience in pharmaceutical, medical device, healthcare, technology, consulting, or another regulated environment
  • Experience supporting process improvement, digital operations, business systems, communities of practice or super-user networks, vendors, document or portal administration, or audit and inspection readiness
  • Working knowledge of quality systems, controlled documentation, data and metadata concepts, and change management
  • Familiarity with GxP or R&D Quality environments is preferred
  • Strong organization, facilitation, communication, stakeholder coordination, problem-solving, and attention to detail
  • Ability to manage multiple priorities, maintain accurate action and decision records, and escalate issues with clear options and recommendations
  • Proficiency with Microsoft Office, collaboration platforms, reporting tools, and business workflow or ticketing tools

Benefits

Comp & perks
  • Inclusive work environment
  • Equal opportunity employment
  • Interview process accommodations for applicants with disabilities