Senior Specialist (it / Ot Compliance)

Merck Merck · Pharma · Singapore

This role is responsible for administering regulatory compliance programs for IT/OT systems within the healthcare industry, focusing on risk-based approaches, audit support, and remediation of compliance risks. It requires experience with regulatory requirements like 21CFR part 11 and GxP environments, and involves collaboration with internal and external auditors.

What you'd actually do

  1. Responsible for representing compliance activities to internal and external auditors / agencies
  2. Supports the development of audit responses and engages with local quality organizations on proper strategies when required.
  3. Responsible for Identifying and engaging in remediation of IT/OT compliance risks.
  4. Execute risk assessments to evaluate the implementation of new technologies or significant changes to existing architectures and technologies
  5. Support local teams with quality and compliance challenges and executions on how to comply with SOPs and or policies

Skills

Required

  • Accountability
  • Application Infrastructure
  • Business Functions
  • Business Processes
  • Business Process Modeling
  • Business Strategies
  • Change Management
  • Clinical Documentation
  • Cloud Security
  • Computer Science
  • Digital Forensics
  • Enterprise Systems
  • Governance Development
  • Identity Access Management (IAM)
  • Incident Response
  • Influence
  • IT Change Management
  • IT Infrastructure Management
  • Manufacturing Analytics
  • Network Systems
  • Occupational Therapy
  • Process Engineering
  • Regulatory Compliance
  • Regulatory Compliance Management

Nice to have

  • Post Graduate Qualification in Business Strategy or IT architecture
  • Prior experience in the pharmaceutical industry, with specific experience in the Manufacturing, Supply Chain, and Manufacturing Quality areas
  • Experience in integrating real time shopfloor and lab systems, at an enterprise level, with appropriate levels of resiliency and performance
  • Experience in manufacturing analytics systems, including supply and demand forecasting, biologics process modelling and advanced image analysis.
  • Exposure to multiple, diverse technologies and processing environments.
  • Knowledge of business process re-engineering principles and processes.
  • Strong understanding of application development methodologies.

What the JD emphasized

  • regulatory requirements (21CFR part 11, EMEA Annex’s 11, etc)
  • GxP environment
  • computerized systems validation