Director, Analytical Development & Quality Control
Treeline Biosciences · Watertown, Massachusetts, United States
Posted 20 days ago · $193,877 to $232,875
or apply directly on Treeline Biosciences's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 20 days Treeline Biosciences's roles stay open a median of 45 days
- Reposted
- No
- Salary listed
- Yes 100% of Treeline Biosciences's roles list one
- Ghost-job risk at Treeline Biosciences
- high 8 stale, 0 reposted of 15 open
- Hiring momentum
- 19 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 Treeline Biosciences's own greenhouse board since 2026-08-03. Full hiring picture for Treeline Biosciences.
About this role
The Director of Analytical Development & Quality Control will lead the strategic and operational aspects of analytical development and quality control for small molecule Oral Solid Dose and parenteral Drug Product programs. This role involves overseeing analytical method development, ensuring compliance with regulatory standards, and managing external partnerships with contract laboratories. The Director will collaborate with various teams to advance drug development milestones and establish scalable analytical capabilities.
- benefits
- 1/5
- 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 Treeline Biosciences as an employer.
What you need
- Ph.D./MS in Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, Biotechnology, Chemical Engineering, or related scientific discipline preferred
- 12+ years (Ph.D.) or 15+ years (MS) of progressive pharmaceutical or biotechnology analytical development experience
- Demonstrated deep experience in analytical development activities supporting Drug Product development and manufacturing
- Proven track record advancing products from early development through late-stage clinical development and/or commercialization
- Strong working knowledge of analytical method development and validation, stability programs, specification setting, and GMP analytical testing
- Excellent project management and organizational skills
Nice to have
- Additional experience in development and implementation of analytical methods to support antibody/ADC manufacturing
- Experience in developing and commercializing drugs for oncology
- Experience with Biologics testing methodologies preferred
- Demonstrated success working with CDMOs and global development partners
Worth weighing
- Role operates in a 100% outsourced environment, which may impact control over processes
- No specific benefits or perks listed in the posting
- Salary range provided, but final offer depends on various factors
- Position classified as exempt, which may imply longer hours or less overtime pay
Summarised from Treeline Biosciences's posting. Read the full original.
Listed by Treeline Biosciences on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
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