Associate Director, Regulatory Operations, EMEA
Ultragenyx Pharmaceutical · Basel, Switzerland
Posted 20 days ago
or apply directly on Ultragenyx Pharmaceutical's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 20 days Ultragenyx Pharmaceutical's roles stay open a median of 41 days
- Reposted
- No
- Salary listed
- No 0% of Ultragenyx Pharmaceutical's roles list one
- Ghost-job risk at Ultragenyx Pharmaceutical
- high 5 stale, 6 reposted of 11 open
- Hiring momentum
- 54 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-09-17
Measured from postings appearing on and disappearing from Ultragenyx Pharmaceutical's own greenhouse board since 2026-08-03. Full hiring picture for Ultragenyx Pharmaceutical.
About this role
The Associate Director of Regulatory Operations at Ultragenyx will lead regulatory submission planning and execution for EMEA, ensuring high-quality submissions to health authorities. The role requires collaboration with various stakeholders, management of publishing activities, and oversight of compliance with regulatory standards. The position also involves driving transformation initiatives and adapting to evolving regulatory landscapes, emphasizing technology and process optimization.
- benefits
- 4/5
- freshness
- 4/5
- career value
- 5/5
- role clarity
- 5/5
- pay transparency
- 0/5
Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Ultragenyx Pharmaceutical as an employer.
What you need
- Bachelor's degree in a scientific, technical, or related discipline, or an equivalent combination of education and relevant experience
- Minimum of 8 years of Regulatory Operations experience within the pharmaceutical, biotechnology, or related life sciences industry
- Extensive knowledge of global regulatory submission requirements, formats, processes, standards, specifications, and health authority expectations
- Demonstrated ability to operate as both a Submission Manager and Publisher across complex global regulatory submissions
- Strong communication, stakeholder engagement, and project leadership skills with the ability to influence, collaborate, and drive alignment across functions and organizational levels
- Exceptional attention to detail, critical thinking, and problem-solving skills, with a demonstrated commitment to quality and compliance
Nice to have
- Experience with eCTD 4.0 submissions, pilot programs, testing initiatives, implementation activities, or transition planning is highly desirable
What you get
- Generous vacation time and public holidays observed by the company
- Volunteer days
- Long term incentive and Employee stock purchase plans or equivalent offerings
- Employee wellbeing benefits
- Fitness reimbursement
- Tuition sponsoring
Worth weighing
- No salary listed
- Role requires a hybrid work model with onsite work 2-3 days a week
- Focus on transformation and technology may imply a fast-paced and evolving work environment
Summarised from Ultragenyx Pharmaceutical's posting. Read the full original.
Listed by Ultragenyx Pharmaceutical on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
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