Chief GMP Data Integrity Officer
RegeneronAbout the role
We are currently looking to fill a Sr Director/Executive Director, Chief GMP Data Integrity Officer position. This position is responsible for the Regeneron Industrial Operations and Product Supply (IOPS) Data Governance and Integrity program. Directs and leads the activities of team. Works closely with business leaders and department subject matter experts to implement data integrity standards into business operations. Serves as the global leader on good practices for their area. Develops and delivers effective training and education programs; works with the business to embed practical steps into procedures, processes and other documentation.
In this role, a typical day might include the following:
Business Priorities:
Global owner and lead for Data Governance and Integrity – defines the standard and ensures broad understanding and integration across the business
Partners with personnel to define or revise associated business processes to meet defined standards; applies practical education and fosters a culture of documenting processes
Works with department management to build a robust data governance program, champion an inspection ready approach and ensure documentation generation and maintenance all supporting compliant data practices
Participates in Regulatory Agency interactions and preparation as related to site inspections and ensures regulatory observations are adequately addressed and completed on schedule
Keeps current on the changing industry landscape and incorporates those findings to continuously improve Regeneron practices and procedures; knowledgeable of process and forensic-based auditing techniques for data integrity
Operational Oversight:
Establishes departmental goals aligned with organization goals
Builds global relationships to gain direct knowledge of operations and influence integration of data integrity standards and continuous improvements of departmental data integrity processes
Provides mentorship to employees for performance and development
Interviews, hires, orients, and trains incoming personnel
Ensure direct-report staff is appropriately resourced, supported and has the tools and direction to properly complete their function
Establishes programs, procedures, and work instructions to lead the data governance program including metrics, reports, inspection readiness, and both conceptual and practical education
Understands data integrity risks and regularly guides departments on requirements and works on the solution; escalates risks to executive leadership on a regular basis
Business Leadership:
Provides leadership and collaboration within and across the organization at all levels, across functional groups for all data integrity matters
Partners with global counterparts to ensure global alignment of processes, systems and procedures, unified communication to user areas, and identification of enhancements
Integrates across IOPS business areas with an eye to gain practical understanding of day-to-day operations
Coach, mentor, and guide staff on changing standards
Identifies risks to operations and collaboratively works with team and business to identify and implement mitigations
Rigorously adheres to organizational basics – models to others the importance of getting the basics right, and reinforcing that standard
Develops personnel, supports a positive, diverse, equal, and inclusive work environment, and builds a strong team.
Technology & Systems
Is responsible for the technology and systems that support the QA team
Health & metrics
Reports status of process performance and ensures timely and accurate metrics for presentation; includes day-to-day operations, program health, status, and action, as well as management review (Right to Operate)
This role may be for you if you:
Have outstanding experience demonstrating ability to partner, influence and incorporate new standards, or extensive experience in changing / revising large-scale program initiatives in the pharmaceutical or biotechnology industry
Have knowledge of one or more of the following pharmaceutical or biotech areas: Manufacturing, Quality Control, Quality Assurance, or Information Technology
Are knowledgeable in applicable federal, state, and local regulations, rules, policies, and procedures such as FDA Guidance on Data Integrity, MHRA Data Integrity Guide, and WHO Guide to Data Integrity
Are able to capture relevant facts, assess, and decide to implement; understands impact to areas and seeks input
Have ability to influence a
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