Associate Director, Drug Product, CMC

🕒 July 28

🇺🇸 United States – Remote

💵 $188.5k - $219k / year

⏰ Full Time

🟠 Senior

👔 Director

👻 Ghost score 2%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

BBOT

WebsiteLinkedInAll Job Openings

51 - 200 employees

🏥 Healthcare

💼 Consulting

🧬 Biotechnology

Healthcare • Consulting • Biotechnology

BBOT is a biotechnology company developing targeted therapies for cancers driven by RAS signaling and PI3Kα. The company focuses on rational drug design to inhibit the active ON state of RAS and to selectively block RAS-driven PI3K activation, aiming at multiple KRAS mutants and novel approaches to maximize target inhibition. BBOT translates decades of RAS biology research into therapeutic candidates intended to improve outcomes for patients with RAS- and PI3Kα-driven tumors.

📋 Description

• Lead the drug product development strategy for assigned small molecule programs, including solid oral dosage forms and other relevant formats • Design, review, and oversee formulation development, process development, and technology transfer activities • Develop phase-appropriate Clinical formulations with a view to overall program success on aggressive development timelines • Author, review, and approve key CMC documentation including development reports, batch records, and regulatory filings (INDs, IMPDs, NDAs, etc.) • Manage outsourced development and manufacturing activities at CDMOs, ensuring technical rigor, compliance, and timeline adherence • Collaborate with internal CMC stakeholders including Process Chemistry, Analytical Chemistry, Reg CMC, and Supply Chain • Collaborate effectively as needed with ex-CMC partners, including Clin Ops, Clin Pharm, Global Reg, Quality, DMPK and Tox • Provide technical leadership on drug product troubleshooting, risk assessments, and change controls • Ensure activities are compliant with GMP, ICH guidelines, and global regulatory requirements • Travel as needed (up to 20%) to support critical manufacturing campaigns and attend company gatherings

🎯 Requirements

• Ph.D. in Chemistry, Pharmaceutical Sciences, Chemical Engineering, or related field with 8+ years of relevant industry experience • M.S. with 12+ years of relevant industry experience • Demonstrated experience in drug product development across Clinical phases, with an emphasis on Pivotal development and commercial readiness • Experience managing CDMOs and overseeing external development and manufacturing • Hands-on experience in drug product development with formulation design and process optimization • Experience with scale up and understanding of potential impact on CQAs • Exceptional problem-solving, organizational, and communication skills • Experience in authoring and reviewing regulatory submissions

🏖️ Benefits

• Competitive salary, benefits, and meaningful equity participation in a company entering the public market • Annual bonus • Stock-based long-term incentives • Medical, dental, and vision benefits • Retirement • Wellness stipend • Flexible time off