or apply directly on Kailera Therapeutics, Inc.'s site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 28 days Kailera Therapeutics, Inc.'s roles stay open a median of 45 days
- Reposted
- No
- Salary listed
- No 0% of Kailera Therapeutics, Inc.'s roles list one
- Ghost-job risk at Kailera Therapeutics, Inc.
- high 14 stale, 0 reposted of 21 open
- Hiring momentum
- 30 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 Kailera Therapeutics, Inc.'s own greenhouse board since 2026-08-03. Full hiring picture for Kailera Therapeutics, Inc..
About this role
The Associate Director of Device Engineering at Kailera will lead the development and launch of drug-device combination products, focusing on autoinjectors, pre-filled syringes, and multidose pens. This role involves cross-functional collaboration to ensure product development meets patient needs and regulatory standards, overseeing project plans, compliance, risk management, and design transfer to manufacturing.
- benefits
- 5/5
- freshness
- 4/5
- career value
- 4/5
- 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 Kailera Therapeutics, Inc. as an employer.
What you need
- Minimum of 10+ years of experience in medical device or combination product development
- At least 3 years in a team leadership role
- Proven experience with autoinjector, pre-filled syringe, or multidose pen development and launch
- Experience authoring clinical and commercial regulatory submissions
- Deep understanding of design controls, design verification, test method development and validation, risk management, human factors, and design transfer
- Strong knowledge of applicable regulatory standards and guidance documents
Nice to have
- Experience working in a regulated pharmaceutical or biotech environment
- Familiarity with combination product regulations (21 CFR Part 4)
- Experience with supplier management of external development, testing, and manufacturing partners
- PMP certification or formal project management training
What you get
- Salary range of $159,000 — $195,000 USD
- Comprehensive health coverage
- Flexible time off
- Paid holidays
- Year-end shutdown
- Monthly wellness stipend
Worth weighing
- Remote work is possible but requires onsite presence at a hub one week every other month
- The role involves significant regulatory compliance responsibilities which may be complex
- No specific mention of team size or structure for leadership context
Summarised from Kailera Therapeutics, Inc.'s posting. Read the full original.
Listed by Kailera Therapeutics, Inc. on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
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