VP, Quality Assurance

Vice President, Quality Assurance

City Therapeutics is a clinical-stage biopharmaceutical company dedicated to developing transformative therapies for patients with serious unmet medical needs. As we progress our pipeline through critical regulatory and clinical milestones, we are seeking a seasoned VP of Quality Assurance to lead and own our quality assurance strategy and systems across the organization.

The Vice President, Quality Assurance will be the senior quality leader at City Therapeutics, responsible for the design, implementation, and continuous improvement of the company's Quality Management System (QMS) and all quality assurance functions. This individual will ensure that all development, manufacturing, and clinical activities are conducted in full compliance with cGXP regulations, applicable regulatory guidance, and internal standards. As a key member of the leadership team, the VP of QA will embed a culture of quality across the organization and ensure the company is perpetually inspection-ready.

Key Responsibilities:

Quality Strategy & Leadership

Define and lead the enterprise-wide Quality Assurance strategy, ensuring alignment with regulatory requirements, industry best practices and business objectives.

Lead quality risk management activities, identifying potential risks and implementing mitigation strategies proactively

Build, develop, and retain a high-performing QA team, establishing clear roles, accountability structures, and career development pathways

Champion and embed a proactive quality culture across all departments, serving as the organizational authority on quality matters

Establish and monitor quality KPIs, metrics, and dashboards; report quality status and trends to executive leadership and the Board as appropriate

cGXP Compliance

Provide executive oversight of all cGXP activities, ensuring compliance with FDA, EMA, ICH, and other applicable international regulations (21 CFR Parts 210/211/312/600, ICH Q7, Q9, Q10, E6, and related guidelines)

Own and continuously improve the Quality Management System, including SOPs, change control, deviation and CAPA management, document control, and training programs

Regulatory Inspections & Agency Interactions

Drive and maintain a state of continuous inspection readiness across all sites and functions

Collaborate with Regulatory Affairs to prepare and review quality sections of IND, BLA, NDA, and other regulatory submissions

Serve as the primary QA lead during FDA, EMA, and other regulatory agency inspections and audits; manage all aspects of inspection response and commitments

Supplier, CMO & CRO Oversight

Establish and maintain a robust vendor qualification and audit program for all CDMOs, CMOs, CROs, and critical suppliers

Negotiate, review, and execute Quality Technical Agreements with all external partners

Cross-Functional Partnership

Partner with Clinical Operations, Regulatory Affairs, CMC, R&D, and Supply Chain to integrate quality requirements into every stage of the product lifecycle

Support due diligence activities and integration planning for partnerships, in-licensing, and M&A transactions as needed

Qualifications:

Bachelor's degree in life sciences, pharmacy, chemistry, or a related field; advanced degree (MS, PhD, PharmD) strongly preferred

15+ years of progressive Quality Assurance experience in the biopharmaceutical or pharmaceutical industry, with a minimum of 5 years in a senior or executive leadership role

Demonstrated experience building and scaling QA functions in a clinical-stage or growth-phase biopharmaceutical company

Working knowledge of international regulatory frameworks including EMA, ICH, and PMDA requirements

Strong leadership presence with the ability to influence cross-functionally, communicate effectively at the executive level, and drive organizational alignment

Proven track record leading successful regulatory inspections (FDA, EMA, or equivalent) and managing health authority interactions and responses

Extensive experience managing CMO, CDMO, and CRO quality relationships and overseeing multi-site QA systems

Comprehensive, hands-on expertise in GMP and GCP regulations, including FDA 21 CFR Parts 210/211/312/600 and ICH Q7, Q9, Q10, and E6(R2)

Preferred

Experience across multiple modalities including biologics, and/or cell and gene therapies

Prior experience supporting a product through BLA/NDA approval and commercial launch

Our Working Model: In Person, By Design

At City, we believe that science and culture thrive together, and that happens best in person. Our working model is clear: we work onsite at our Kendall Square offices five days per week. This choice reflects our belief that great science and cultures run on connection, fairness, and growth.

Connection: Face time matters. Building an enduring biotech company is about people, science, and strategy. Working side by side sharpens ideas, accelerates feedback, and fuels innovation for patients.

Fairness: One model for all. Every voice counts, and fairness depends on shared experience. We hold ourselves to one standard across all levels and functions.

Growth: Learning moves faster in person. Growth comes from conversation, observation, and mentorship. We believe in developing talent, and that happens best when we are together.

We also know that life is not always predictable. When individual needs arise, we are flexible and supportive and work together to balance home life with life at City.

We believe diverse teams drive better science. We welcome applicants from all backgrounds and experiences who share our mission to bring transformative RNAi medicines to patients.

Compensation 

The base salary range provided reflects our current estimate of what we anticipate paying for this position. Your actual base salary will be based on several factors, including job-related skills, experience, internal equity, relevant education or training, and market dynamics. In addition, you will be eligible for an annual bonus, equity compensation, and a competitive benefits package. Pay range is $340,000 to $360,000

City Therapeutics is an Equal Opportunity and Affirmative Action employer. All qualified applicants will receive consideration without regard to race, color, religion, national origin, gender, gender identity or expression, sexual orientation, age, disability, veteran status, or any other characteristic protected by law.

City Therapeutics is accepting resumes/CVs from direct applicants only.  Recruitment Agency submissions will not be accepted at this time.