Sr Director, QA- GxP Systems

With positive Phase 3 results from our lead program and BLA readiness underway, Candel is reaching an important inflection point—one that creates the opportunity to translate scientific innovation into meaningful impact for patients, while the company continues to advance the next generation of programs across solid tumors. We believe breakthrough science is powered by people who challenge convention, bring different perspectives, collaborate across disciplines, and focus on shared outcomes.

• Location: Hybrid (3 days/week in Needham, MA; 2 days remote)
• Salary: 258,333 - $280,000 + 25% bonus

Why Work With Us?   
Our people are at the heart of that journey!  We believe breakthrough science is powered by people who challenge convention, bring different perspectives, collaborate across disciplines, and focus on shared outcomes.  Candel’s culture is grounded in trust, flexibility, accountability, creativity, and a shared commitment to one goal: improving the lives of patients and their families

Our Science: Advancing Cancer Immunotherapies   
Candel is a clinical-stage biopharmaceutical company developing innovative multimodal viral immunotherapies designed to harness the power of the immune system against cancer. With positive Phase 3 results from our lead program and BLA readiness underway, Candel is reaching an important inflection point—one that creates the opportunity to translate scientific innovation into meaningful impact for patients, while the company continues to advance the next generation of programs across solid tumors. This is an exciting time for Candel as we evolve from a focused clinical-stage biotechnology company toward an integrated biopharmaceutical organization. Learn more: www.candeltx.com   

Position Summary:
This is a highly visible, unique opportunity for a seasoned quality systems professional who 
thrives in fast-paced, resourceful environments. You’ll report directly to the SVP of Quality and 
serve as a strategic partner across departments and overall GxP system effectiveness. You are a builder—of 
systems, of processes, of trust.

We don’t believe in micromanagement here. We believe in hiring people who take ownership, 
follow through, and bring integrity to every detail. If you're ready to roll up your sleeves, drive 
change, and help bring a life-changing oncology therapy to market, read on.
This is not a role for the average. This is a role for someone ready to help launch a first-in-class 
therapy, and do it the right way.

What You’ll Own
• Quality Operations Leadership:
Manage the lifecycle of GxP systems across QA, Clinical Ops, CMC, and 
Research, ensuring full compliance with 21 CFR Part 11 and modern industry standards.
• Vendor Oversight & Auditing:
Lead qualification, risk assessment, and ongoing oversight of a diverse ecosystem of 
internal and external vendors—ranging from eQMS and EDMS to training systems, 
supply chain tools, and cloud-based clinical applications.
• Cross-functional Enablement:
Support scientific teams (PD, analytical, R&D) by ensuring vendor and data integrity for 
BLA-enabling work. Bridge clinical and commercial quality expectations through 
practical systems thinking.
• Training & Continuous Improvement:
Deliver GxP systems training and drive continuous improvement initiatives, trend 
analysis, and knowledge management across the org.
• Documentation & Record Management:
Oversee document bundling, review, and archiving for key deliverables like batch 
records, stability studies, and QA releases. Ensure audit-ready files and streamlined 
workflows

What You Bring
• Bachelor's degree in Life Sciences or a related technical field.
• 10+ years of experience in biotech/pharma Quality Assurance, with direct ownership of 
GxP systems and a proven track record managing audits, vendors, and validations.
• Expertise with eQMS, EDMS, training systems, and other regulated platforms; familiarity 
with stability, batch records, and clinical supply workflows.
• Background in clinical-stage or hybrid clinical/commercial environments, with a handson approach to QA operations and system management.
• Strong understanding of ICH, FDA, and Part 11 requirements, and how they apply to 
cloud-based, outsourced, and evolving environments.
• Experience in cross-functional quality enablement, supporting teams like PD, Analytical, 
and Clinical in system compliance.
• Critical thinker with the ability to navigate ambiguity, prioritize work, and maintain 
momentum without daily direction.

NOTE: All applicants must be authorized to work in the US and do not require sponsorship. 
Unfortunately, we are unable to provide sponsorship of any kind at this time

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