or apply directly on Avalyn Pharma's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 30 days Avalyn Pharma's roles stay open a median of 37 days
- Reposted
- No
- Salary listed
- No 0% of Avalyn Pharma's roles list one
- Ghost-job risk at Avalyn Pharma
- moderate 2 stale, 0 reposted of 9 open
- Hiring momentum
- 12 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 Avalyn Pharma's own greenhouse board since 2026-08-03. Full hiring picture for Avalyn Pharma.
About this role
The Senior Manager, Regulatory Affairs at Avalyn will support the global regulatory strategy for inhaled drug-device combination products. This role involves contributing to regulatory submissions, health authority interactions, and cross-functional planning to ensure compliance and operational excellence throughout the product development pipeline. The position requires collaboration with various teams and offers opportunities for increased ownership of development programs as responsibilities grow.
- benefits
- 1/5
- freshness
- 4/5
- career value
- 4/5
- role clarity
- 4/5
- 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 Avalyn Pharma as an employer.
What you need
- Bachelor’s degree
- 5-8 years of regulatory affairs experience in the pharmaceutical, biotechnology, or combination product industry
- Experience with global clinical trials and regulatory submissions (INDs, CTAs, amendments)
- Understanding of U.S. FDA regulations and ICH guidelines
- Ability to collaborate within cross-functional teams
- Strong project management and organizational skills
Nice to have
- Advanced degree (e.g., MS, PharmD, PhD) or regulatory affairs training/certification
- Experience with drug-device combination products
- Experience with orphan drug or expedited regulatory pathways
- Experience with regulatory information management systems or SharePoint
- Experience in a small biotechnology company
Worth weighing
- No specific benefits listed
- Salary range provided is $157,000 — $173,000, which may vary based on experience
- Role involves significant collaboration across multiple teams, which may require strong interpersonal skills
Summarised from Avalyn Pharma's posting. Read the full original.
Listed by Avalyn Pharma on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
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