Associate Director, GVP Compliance

Who We Are

BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions. Guided by our purpose to develop medicines that make a profound impact on people's lives, our global teams have delivered a portfolio of therapies since our founding in 1997. Our revolutionary treatments for conditions like achondroplasia (the most common form of dwarfism), PKU (phenylketonuria), CLN2, a form of Batten disease, and a number of forms of MPS (mucopolysaccharidosis) offer new possibilities for patients and families who previously had few, if any, available options. More recently, with the close of the Amicus acquisition, our portfolio has expanded to include therapies for Fabry disease and Pompe disease, expanding our ability to reach more people living with rare genetic conditions.

Our success comes from our unwavering commitment to excellence, our deep understanding of patient needs, our scientific expertise, and our world class manufacturing capabilities. At the heart of BioMarin is a dedicated team of the brightest minds in the industry working together to deliver innovative therapies to patients and families around the world.

About Technical Operations

BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.

Associate Director, GVP Compliance

Shanbally, Ringaskiddy, Cork

Hybrid role (2 days per week onsite)

Closing date: 24 June 2026

SUMMARY

BioMarin is a world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life threatening rare genetic diseases. We are looking for an individual with experience working in Pharmacovigilance (PV) within Quality and Compliance. This role joins our Global Quality organization and reports to the GVP Compliance Lead. It advises internal and external stakeholders on Good Pharmacovigilance Practices (GVP) matters and assesses compliance with global regulations, corporate policies, and SOPs. The individual performs GVP audits and is key for preparing and executing GVP regulatory inspections, identifying and partnering with stakeholders to resolve compliance risks and related issues.

BioMarin is a global, high performing, team based organization where colleagues are flexible, multi skilled, and empowered to make decisions. A high level of initiative, clear communication, effective collaboration, strategic thinking and strong decision making are important skills the candidate would possess.

Candidates must adhere to established processes and policies, demonstrating professionalism and integrity in all situations. They should ensure patient safety in pharmaceutical practices through a comprehensive strategy that integrates regulatory compliance, risk management, pharmacovigilance, and continuous improvement.

RESPONSIBILITIES

• Advancing the execution of the Global Quality vision, policies, processes, and decisions
• Collaborate with stakeholders to identify, communicate, and mitigate compliance risks
• Continually enhance partnerships with key stakeholders and leaders across the business
• Support and drive the implementation of quality and compliance projects and objectives
• Stay updated on regulations and recommend proactive compliance changes when necessary
• Execute against GVP Compliance processes and best practices
• Perform GVP audits and contribute to effective implementation of the Global GVP Audit Program
• Act as a GVP compliance core team member on regulatory inspection teams and support mock readiness activities
• Provide insights to continually optimize the GVP Compliance Audit Program
• Contribute to Pharmacovigilance System Master File (PSMF) updates
• Contributor to the Risk Evaluation and Mitigation Strategies (REMS) compliance program
• Contribute to building a team that ensures GVP compliance and fosters a culture of teamwork and mutual respect
• Mentor and support the development of junior staff to achieve their full potential

EXPERIENCE

Required Skills:

8+ years of experience working within a regulated healthcare industry including a role in capacity of quality and compliance.

• Working knowledge of FDA, EMA, and global PV Regulations, and application of Good Pharmacovigilance Practices (GVP), ICH, and GCP regulations
• Experience working in Pharmacovigilance (PV) within Quality and Compliance
• Experience executing or managing Health Authority Inspections
• Experience executing or managing R&D Audits and GVP Audit Program
• Experience with identifying optimal strategy for executing a GVP audit program working with internal auditors and external consultants
• Experience navigating and understanding a quality management system
• Core competencies in strategic thinking, agility, prioritization, communication and decision making
• Strong verbal, written and oral communication skills. Able to present to Senior Leadership.
• Able to work independently and be flexible to rapidly changing priorities
• Strong computer skills including working within the MS Suite of tools, and interfacing with Quality Management Systems

Desired Skills:

• Experience with Business Development partnerships, mergers and/or acquisitions
• Exposure to working in any phase of pharmaceutical drug development or post marketing surveillance of medicines
• Awareness and understanding of core PV responsibilities i.e., risk management, risk minimization measures, signal management, and case processing
• Compliance oversight of REMS Program(s)

EDUCATION

Bachelor's Degree within a life science focus area; master's degree is a plus.

CONTACTS

• Head of R&D Quality
• GCP Compliance Team
• GLP Compliance Team
• Head of Global PV Operations
• Regulatory Affairs
• Commercial Operations

SUPERVISOR RESPONSIBILITY

None

SHIFT DETAILS

Shift will be 8 hours per day. If EU employee identified, shifts include at least (2) days per week with required partial overlap with the US EST and PST hours of operation.

ONSITE, REMOTE, OR FLEXIBLE

This role has flexibility to be a remote position covering both EU and US time zones. There is no requirement to be strictly onsite; however, staff local to the SRC, Shanbally, Dublin, London and Novato offices will be expected to be onsite following the hybrid role requirements.

TRAVEL REQUIRED

May travel up to 25%+ of the time.

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity, sexual orientation, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.