$242K – $313.5K/yr
Director, External & CMC Quality Assurance
Role overview
Job description
- Provide Quality Assurance oversight over Drug Substance manufacturing of GxP biological product. This involves oversight of multiple CMOs as part of a complex supply chain that includes contract laboratories and other critical service providers.
- Provide QA oversight of deviations, investigations, CAPAs, change controls, testing, product impact assessments, and disposition-related decisions.
- Design and maintain a robust, scalable product disposition program for clinical trial material as well as commercial products across multiple markets.
- Ensure continuous inspection readiness across outsourced operations and support health authority inspections, partner inspections, and due diligence activities.
- Monitor partner quality performance through defined metrics, scorecards, and governance forums; identify trends and proactively escalate compliance or execution risks.
- Partner cross-functionally to assess quality risk associated with process changes, deviations, investigations, comparability activities, tech transfer, and supply continuity issues.
- Provide strategic guidance on quality requirements for product lifecycle activities, including clinical supply, commercial readiness, distribution, complaints, and post-approval changes.
- Drive a culture of quality, accountability, and proactive issue identification across internal stakeholders and external partners.
Candidate Qualifications
- BS/MS degree in a scientific discipline.
- 12+ years of experience in the pharmaceutical/biotech industry (including meaningful experience in outsourced/virtual operating models), with 5+ years in leadership roles within Quality or related functions
- Strong working knowledge of GMP/GxP requirements, FDA/EMA expectations, ICH guidance, and risk-based quality management principles.
- Demonstrated success overseeing external manufacturers, testing laboratories, suppliers, and quality service providers.
- Experience supporting biologics products across both clinical and/or commercial stages; demonstrated success driving continuous improvement.
- Strong communication skills, sound scientific judgement, and the ability to balance strategic thinking with hands-on execution.
- Highly proactive, decisive, and capable of independently managing key initiatives in a fast-paced commercial readiness and launch environment.
- Engaged leader committed to building a strong quality culture through collaboration and mentorship.
Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
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About this listing
- Source: Scholar Rock's official careers site · still listed there on 11 Nov 2026
- Posted 8 Oct 2026
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What they are looking for
Skills & requirements
Qualification
Candidate Qualifications BS/MS degree in a scientific discipline; 12+ years of experience in the pharmaceutical/biotech industry (including meaningful experience in outsourced/virtual operating models), with 5+ years in leadership roles within Quality or related functions Strong working knowledge of GMP/GxP requirements, FDA/EMA expectations, ICH guidance, and risk-based quality management principles
Department · Development
Hiring company
Scholar Rock
We create new possibilities through cutting-edge science. At Scholar Rock, we are on a mission to discover, develop, and deliver therapies to improve people’s lives. We are a biopharmaceutical company combining bold science with a deep commitment to make a meaningful difference for people living with serious diseases. Learn more We take a unique approach […]
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