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SENDA Biosciences

Director/Senior Director, Quality

Posted 11 Days Ago
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In-Office
Cambridge, MA
200K-290K Annually
Senior level
Easy Apply
In-Office
Cambridge, MA
200K-290K Annually
Senior level
Lead and mature Sail's Quality organization and eQMS across GxP operations. Ensure GCP/GMP/GLP compliance, oversight of CMC and clinical programs, partner qualification, inspection readiness, QA/QP batch release, and global post-market quality systems while building a high-performing team and continuous improvement metrics.
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About Sail:

Sail Biomedicines is pioneering the integrative design and deployment of fully programmable medicines to transform patient care. Sail’s platform combines first-in-class programmable circular RNA technology (Endless RNA™ or eRNA), and an industry-leading platform of programmable nanoparticles, utilizing natural components, to unlock comprehensive programming of medicines for the first time. By leveraging cutting-edge eRNA and nanoparticle deployment technology, Sail is building a wealth of data, enabling unparalleled use of generative AI techniques to identify and design fully programmable medicines that are potent, targeted, versatile, and tunable. Sail was founded by Flagship Pioneering.

The Role:

We are looking for a strategic, execution-focused Head of Quality to oversee and advance our Quality organization. This leader will be responsible for establishing and maturing Sail’s Quality systems and practices across all GxP operations in collaboration with internal stakeholders and external partners. The Head of Quality will own the internal eQMS and be responsible for ensuring GCP, GMP & GPL compliance.

Responsibilities:

  • Develop and execute Sail’s GxP Quality strategy across pre-clinical and clinical programs, ensuring alignment with global regulatory expectations (FDA, EMA, ICH).
  • Collaborate cross-functionally with Manufacturing, Supply Chain, Regulatory, and Clinical leaders to embed Quality into end-to-end business processes.
  • Serve as the executive Quality representative for regulatory inspections and major health authority interactions.
  • Manage, execute and maintain critical partner qualification
  • Lead quality oversight across Sail’s clinical and nonclinical development programs. This includes GCP compliance, CRO/vendor qualification, clinical site audits, TMF management, inspection readiness, and GLP oversight for IND-enabling studies.
  • Provide quality oversight of the CMC supply chain across internal operations and external CDMOs; ensure compliant batch disposition and vendor compliance.
  • Ensure compliance with global importation/exporation requirements and maintain oversight of QA and/or QP batch certification and release processes.
  • Provide strategic oversight for release and stability testing, method validation/transfer, reference standards, and specification lifecycle management.
  • Quality Management Systems (QMS) ownership: Own and evolve Sail’s QMS, including deviation/CAPA management, change control, documentation, training, and internal/external audit programs.
  • Establish and oversee global processes for product quality complaints, field alert reporting, investigation closure, and compliance with post-market reporting requirements.
  • Build and lead a high-performing Quality organization, ensuring clinical and CMC process excellence, regulatory compliance, and a culture of accountability and transparency.
  • Define and monitor Quality performance metrics, implement continuous improvement initiatives, and ensure systems readiness for global scale.

Required Qualifications:

  • 15+ years of progressive leadership in biopharmaceutical Quality, including experience supporting global early-stage clinical programs
  • Deep expertise across both GCP and GMP as well as the supporting Quality Systems, with a track record of successfully leading organizations through regulatory inspections (FDA, EMA, etc.).
  • Demonstrated success managing external partners (CDMOs, CROs, testing labs).
  • Strong understanding of regulatory expectations for global post-market quality systems, including complaint management and field alert reporting.
  • Proven ability to scale Quality organizations and systems to support global operations.
  • Experience managing an eQMS
  • Desire to operation in a phase-appropriate, flexible and/or creative manner while ensuring organization wide compliance
  • Excellent communication, leadership presence, and cross-functional collaboration skills.
  • Bachelor’s degree in life sciences or related field required; advanced degree preferred.

Salary Range: $200,000 - $290,000

Sail Biomedicines is an Equal Opportunity Employer. Sail does not discriminate based on race, religion, color, sex, gender identity, sexual orientation, age, national origin, veteran status, or any other status protected under federal, state, or local law.

Top Skills

Capa
Change Control
Eqms
GCP
Glp
Gmp
Gxp
Qms
Tmf
HQ

SENDA Biosciences Cambridge, Massachusetts, USA Office

20 Acorn Park Dr, 300, Cambridge, MA, United States, 02140

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