Responsibilities
Process Optimization and Design
Lead the design, development, implementation and optimization of processes for the regulatory organization.
Work with cross‑functional teams responsible for processes involving regulatory responsibility across the organization; provide oversight and alignment on regulatory systems and interdependencies; contribute to communication and training relating to Regulatory process development.
Establish SME networks and lead pilots and outcome learnings; obtain ideas from stakeholders for system and/or process improvement; close collaboration with GRA Compliance, L&D, Metrics teams, and SMEs team to identify opportunities for continuous improvement.
Regulatory Process Adherence Oversight
Involve cross‐functional colleagues and partner on development and monitoring of regulatory process adherence oversight.
Close collaboration with other Regulatory functions, as appropriate, on training and communications of new processes and continuous improvements.
Share awareness of and insight in authorities’ inspections and internal audits of regulatory processes, including outcome and findings in the area of responsibility; support of CAPA related activities for regulatory and cross‑functional alignment.
Utilize data analytics/metrics to provide an understanding of data flow and trends leading to identification of process improvements.
Qualifications
Experience in a Regulatory Affairs function within Pharmaceutical, Biotech, or other highly regulated industries required.
Previous experience in process design and project management preferred.
Compliance background preferred.
Comprehensive knowledge of departmental and organizational policies, procedures and systems.
Six Sigma or other project management certification preferred.
Basic flowcharting skills (e.g., Visio) preferred.
Benefits
Excellent career progression opportunities
Work‑life balance initiatives
Bonus scheme
Health insurance
Pension
Viatris is an Equal Opportunity Employer.
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