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Novartis

eCompliance Manager

AI in this role

eCompliance Manager overseeing computerized system validation and driving the deployment of AI-enabled solutions within GxP processes.

computerized-system-validationgxpquality-assurancecomplianceai-governance

Job Description Summary

About the role:

The eCompliance Manager is responsible for providing Quality Assurance oversight and guidance with regard to computerized systems validation (CSV), operating within the framework of regulations (GxP, 21CFR11, etc.) and requirements defined in the Novartis Quality Manual and global procedures.

eCompliance Manager provides the needed operational support such as approving the GxP impacted changes, Periodic Review Reports, deviations etc., Provides the guidance to the project and operations team on the CSV related topics and related information. Reviews and/or approves the global Computerized Systems key validation deliverables as a part of the eCompliance support to the GxP projects.


Job Description

Key Requirements:


  • Quality oversight of operational activities of GxP systems (e.g., Changes, Periodic Reviews, Deviations etc.,). Drive the design, deployment and continuous improvement of automation and AI-enabled solutions within assigned processes.​
  • Provide needed support to meet the applicable Novartis and regulatory requirements for GxP regulated computerized systems projects. Supports the development of future-focused strategy in AI and emerging technologies readiness, evaluating regulatory requirements and developments to ensure Novartis QMS is fit for purpose in the eCompliance environment.
  • Point of Contact for all CSV related matters for GxP Computerized Systems and act as an interface between IT and Business for eCompliance topics in relation to GxP classified Computer Systems promoting a Quality Culture.
  • Review and approve project related documents for GxP relevant systems including determination of GxP applicability for all GxP and non-GxP relevant systems.
  • Establish trusted partnership with assigned IT Function with understanding of business drivers, and provide the needed day to day operational support. Review and approve the GxP Changes and the associated deliverables.
  • Review and approve the GxP impacted deviations, ensure appropriate CAPA are implemented. Review and approve the Periodic Review Reports for the GxP computerized systems and the associated gaps within CAPA Management System.
  • Perform supplier qualification assessment activities. Provide Audit support as assigned and in case of CAPAs, provide the required Quality support.

Essential Requirements:

  • 10-15 years of overall IT experience, and a minimum 7 years of relevant experience in the Pharmaceutical Industry and in particular within regulated functions such as IT Quality and Compliance
  • Education- Degree in Information Technology, Life Sciences, Pharmacy, Engineering or equivalent
  • Solid understanding of global regulations and Health Authorities expectations governing computerized systems (CSV, Part 11, etc.)
  • Solid experience in the development, implementation and lifecycle management of computerized systems in regulated environments
  • Experience in quality management of Cloud, SaaS platform, mobile and digital application used in regulated environments. Highly experienced in the operational management of GxP solutions including its related technologies to support the operation
  • Good understanding in system application management, its Quality support approach and industry best practices (ITIL, ITSM, etc.)
  • Experience in the development, implementation and lifecycle management of key computerized systems in the Pharmaceutical Development, Manufacturing, Quality, Commercial and Infrastructure space (e.g. ERP/SAP, MES, LIMS, CRM, IAM, etc.)

Desirable Requirements:

  • Successful cross-divisional/functional work with complex international teams. Experience in GxP supplier qualification activities
  • Proven ability to adjust to multiple demands, shifting priorities and unexpected events while maintaining a positive work attitude
  • Ability to effectively interact and present to Management
  • Ability to manage the key stakeholders and build trust
  • Proven ability to influence without hierarchical authority and build trusted partnerships
  • Proven self-starter with experience in initiating and delivering projects and processes
  • Excellent communication, negotiation, facilitation, and interpersonal skills


Skills Desired

Audits Compliance, cGMP Compliance, Collaboration, Communication, Data Integrity, Decision Making, Internal Auditing, Managing Ambiguity, Problem Solving, Quality Assurance (QA), Quality Auditing, Quality Compliance, Quality Management, Quality Management System Implementation, Quality Management Systems (QMS), Regulatory Compliance, Risk Management, Validation Activities

How we rate this

eCompliance Manager at Novartis rates 65 out of 100 for how much of the daily work is AI. That makes it Works on AI (AI Level 3 of 4). The level is about AI in the job, not seniority.

Classification

Works on AI. The daily work is on AI products, without building the model.

  1. ●●●● Builds AI80 to 100
  2. ●●●○ Works on AI60 to 79
  3. ●●○○ Uses AI40 to 59
  4. ●○○○ Little AI0 to 39

Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.

Prepare for this job

Built from this posting and from similar jobs on Level.

Skills and AI tools this role asks for

Computerized System ValidationGxpQuality AssuranceComplianceAI Governance

Questions you could be asked

  1. Tell me about a project where computerized system validation was part of your work. What did you do?
  2. Tell me about a project where gxp was part of your work. What did you do?
  3. Tell me about a project where quality assurance was part of your work. What did you do?
  4. Tell me about a project where compliance was part of your work. What did you do?
  5. Tell me about a project where ai governance was part of your work. What did you do?

Adapt your resume

  • List these exact terms on your resume: Computerized System Validation, Gxp, Quality Assurance, Compliance, and AI Governance. An applicant tracking system matches the wording, not the idea.
  • Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.
  • Show where AI is part of your daily process, not a one-off project. This role expects it to be a running habit.

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