Keeps up-to-date on regulations/ development of biopharmaceutical QC method/ technology to ensure the project maximizes the use of digitalization, automation and robotics.
Create and maintain comprehensive project documentation throughout the project lifecycle, including business requirements, user acceptance test scenarios/cases, business process workflows, and project timelines.
Evaluate investigation outcomes and provide well-reasoned findings, conclusions and recommendations, including disciplinary actions, corrective measures, and risk mitigation strategies where appropriate.
Apply established Manufacturing QA standards, methods, playbooks and tools to support consistency, standardisation and adoption of proven approaches across manufacturing teams.
Design, implement, and support cybersecurity solutions across cloud and on-prem environments (SIEM/SOAR, endpoint, cloud security, Zero Trust, vulnerability management)
Coordinate with external auditors, tax agents, and regulatory bodies to ensure timely completion of audit, tax, ECDA requirements, and statutory reporting obligations.