Associate Director, Analytical Development & Quality Control
Entrada Therapeutics · Boston, MA
Posted 15 days ago · $172,000 - $202,000
or apply directly on Entrada Therapeutics's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 15 days Entrada Therapeutics's roles stay open a median of 35 days
- Reposted
- No
- Salary listed
- Yes 67% of Entrada Therapeutics's roles list one
- Ghost-job risk at Entrada Therapeutics
- moderate 2 stale, 0 reposted of 9 open
- Hiring momentum
- 14 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 Entrada Therapeutics's own greenhouse board since 2026-08-03. Full hiring picture for Entrada Therapeutics.
About this role
As the Associate Director of Analytical Development & Quality Control at Entrada Therapeutics, you will lead late-stage AD&QC activities for oligonucleotide programs, ensuring compliance with regulatory standards and readiness for NDA submissions. Your role involves collaborating with cross-functional teams and external partners, managing analytical methods, and authoring regulatory documents. You will also establish quality metrics and drive continuous improvement initiatives to enhance operational efficiency and inspection preparedness.
- benefits
- 4/5
- freshness
- 4/5
- career value
- 4/5
- role clarity
- 5/5
- pay transparency
- 5/5
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 Entrada Therapeutics as an employer.
What you need
- Ph.D. in Organic Chemistry, Analytical Chemistry, or a related discipline
- Minimum of 6 years of late-stage and commercial AD&QC experience in a Biotech or Pharmaceutical industry
- Strong knowledge of AD&QC requirements for late-stage and commercial oligo programs
- Extensive experience in regulatory filing, including IND, IMPD, NDA, and MAA
- Strong knowledge of regulatory requirements and guidelines (ICH/FDA/EMA/USP/Ph. Eur.)
- Extensive knowledge of cGMP regulations and guidelines
Nice to have
- Experience with PMO and PPMO programs
- Experience contributing to product quality risk assessments
What you get
- Comprehensive health, dental and vision coverage
- Life and disability insurance
- 401(k) match
- Paid, gender-inclusive parental leave
- Holistic support for health and well-being
- Education reimbursement
Worth weighing
- Remote position with preference for local New England candidates who can be in the office once a week
- Monthly or quarterly travel required to Boston headquarters
- Salary range provided, but final compensation may vary based on candidate factors
Summarised from Entrada Therapeutics's posting. Read the full original.
Listed by Entrada Therapeutics on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
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