Associate Director, In-Market & Distribution Quality Leader (EU/MEA Region)
Location Dublin, Ireland Workstyle Hybrid ApplyWho We Are
BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health.
Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities.
Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best – people with the right technical expertise and a relentless drive to solve real problems – and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we’ve produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options.
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, In-Market & Distribution Quality Leader (EU/MEA Region)
Location: Dublin or Cork ( Hybrid role 2 days per week in the office)
Closing date: Thursday 20th November 2025
SUMMARY DESCRIPTION
|
RESPONSIBILITIES |
|
SCOPE |
This role is responsible for supporting the efficient distribution of lifesaving therapies in compliance with applicable regulations. Decisions made in this role are of critical nature in mitigating risks for the business while ensuring BioMarin’s commercial and clinical products are delivered to patients in a timely and compliant manner. The candidate should demonstrate the following attributes: ·A firm commitment to BioMarin’s cultural beliefs and values ·Consistent track record of exceeding objectives within area of influence ·Ability to achieve results through others without direct reporting lines ·Strong problem-solving skills with a global focus both internally and externally ·Possess a high level of accountability and demonstrate an ability to be a change agent in a highly regulated industry ·Flexibility and ability to deal with changing priorities without losing sight of the overall business ·Strong interpersonal, communication and influencing skills working with all levels and within an environment of constant change ·Proactive and energetic outlook with an unwillingness to accept the status quo ·Interaction and collaboration with team members, peers and senior management ·Ability to work independently with strong time management skills Approximately 20% travel |
EDUCATION |
·Bachelor's degree in Pharmacy, Life Sciences, or a related field. A master's degree is a plus. |
EXPERIENCE |
·Minimum 8–10 years of experience in pharmaceutical quality assurance, with at least 5 years focused on GDP in the EUMEA region. ·In-depth knowledge of EU GDP Guidelines and regional regulatory requirements. ·Experience managing audits, inspections, and quality systems in a multi-country environment. ·Strong leadership and team management skills, excellent communication and interpersonal skills. ·Proficiency in QMS tools and systems, and a solid understanding of logistics and supply chain principles. ·Detail-oriented, analytical thinker, problem-solver, and able to work in a fast-paced environment. ·Strategic mindset with hands-on operational execution. ·Proven ability to lead change initiatives and drive improvements within and across functions which enable compliance and mitigate risk ·Ability to effectively work autonomously and independently ·Understanding of Quality Tool: Veeva, TrackWise, MasterControl QMS, SAP, or like technologies |
CONTACTS |
Commercial, Site Operations, Clinical Operations, Worldwide Research & Development Scientists, Contract Manufacturing, Quality Assurance, Finance External partners including 3PL providers, transport carriers. Health Authorities and National Regulatory Bodies |
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.
Equal Opportunity Employer/Veterans/Disabled
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
Equal Opportunity Employer/Veterans/Disabled
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.