Quality Site Head

Crispr Therapeutics Inc; Framingham (MA); On-site; USD 230,000 - 260,000; Full time

Benefits offered by this job

Equity

Bonus

Benefits

Job summary

CRISPR Therapeutics Inc. is seeking a Quality Site Head to lead the Quality function at the internal manufacturing site and guide QA strategy across operations in Boston-based facilities.

The role emphasizes excellence in GMP manufacturing, regulatory readiness, and continuous improvement to support transformative gene-based therapies. The position requires extensive QA leadership experience in GMP biopharma, with a focus on inspections, life-cycle management, and cross-functional collaboration

Qualifications

• BS/MS in relevant scientific discipline with 15–20+ years in biopharma QA at GMP facilities.
• Deep knowledge of FDA/EMA/ICH regulations and product development lifecycle.
• Ability to operate strategically and hands-on within GMP environments.

Responsibilities

• Foster a Quality culture emphasizing innovation, improvement, and accountability.
• Provide strategic direction and operational leadership for site Quality and QA at the facility.
• Oversee end-to-end Quality activities including FUSE qualification/validation, materials management, batch record reviews, change control, and exceptions.
• Ensure Product Disposition aligns with GMP and regulatory submissions.
• Establish quality metrics to demonstrate GMP adherence and CRISPR procedures.
• Collaborate with partners to enable compliant manufacturing, tech transfers, validation, testing, and lifecycle management.
• Lead site inspection readiness and host Health Authority inspections.
• Coordinate with Quality Systems, Compliance, and External Quality Operations to advance GMP processes.
• Provide leadership to drive a fast-paced, learning culture; champion data-driven decisions.
• Promote a collaborative, transparent, ownership-focused work environment.

Skills

Quality Assurance

GMP Compliance

Leadership

Regulatory Experience

Cross-functional Collaboration

Inspection Readiness

Education

BS/MS in Life Sciences

Advanced degree (PhD)

Job description

Job Description:

Company Overview

Founded over a decade ago,CRISPR Therapeuticsis a leading biopharmaceutical company focused on developing transformative gene-based medicines for serious human diseases. The Company has evolved from a pioneering research-stage organization into an industry leader, marking a historic milestone with the approval of CASGEVY®(exagamglogene autotemcel (exa-cel)), the world’s first CRISPR-based therapy, approved for eligible patients with sickle cell disease and transfusion-dependent beta thalassemia.CRISPR Therapeuticsis advancing a broad and diversified pipeline across hemoglobinopathies, cardiovascular, autoimmune, oncology, regenerative medicine and rare diseases. The Company continues to expand its leadership in gene editing through the development of SyNTase™ editing, a novel and proprietary gene-editing platform designed to enable precise, efficient, and scalable gene correction. To accelerate and expand its impact,CRISPR Therapeuticshas established strategic collaborations with leading biopharmaceutical partners, includingVertex Pharmaceuticals.CRISPR Therapeutics AGis headquartered inZug,Switzerland, with its wholly-ownedU.S.subsidiary,CRISPR Therapeutics, Inc., and R&D operations based inBoston, MassachusettsandSan Francisco,California.

Position Summary

Reporting to the Vice President, Head of Quality, the Quality Site Head will play a key leadership role both at CRISPR’s internal manufacturing site and within the Quality Assurance function as a whole. The ideal candidate will lead by example to promote excellence in every aspect of internal manufacturing operations as part of CRISPR’s mission to develop impactful therapies at the forefront of gene-editing technology.

Responsibilities

• Foster a Quality culture that values innovation, continuous improvement, and personal accountability
• Provide strategic direction and operational leadership for the site Quality function at CRISPR’s internal manufacturing facility
• Responsible for end-to-end Quality within the site, including FUSE qualification/validation, materials management, batch record reviews, change control, and exceptions
• Responsible for Product Disposition ensuring that intermediates and drug products are manufactured and tested in accordance with GMP and regulatory submissions,
• Establish quality metrics to demonstrate adherence to GMP regulations and CRISPR procedures
• Collaborate with internal partners to enable compliant and successful manufacturing (e.g. technology transfers, validation, testing, and lifecycle management)
• Lead and maintain site inspection readiness, and host audits and Health Authority inspections
• Work closely with Quality Systems and Compliance and External Quality Operations to advance all aspects of CRISPR’s GMP Quality processes
• Provide leadership and management support for activities to drive a fast paced, highly efficient learning culture.
• Be a champion of a highly collaborative, transparent, data driven, make it happen’ culture.

Minimum Qualifications

• BS/MS in relevant scientific discipline and 15-20+ years of experience in a biopharmaceutical organization; including direct experience in Quality Assurance at a GMP manufacturing facility
• Expertise in FDA/EMA/ICH regulations and guidelines and a strong understanding of pharmaceutical product development lifecycle are required
• Able to simultaneously operate at both a strategic and hands-on level in a GMP environment
• Inclusive leadership skills and keen organizational awareness, enabling the development of strong working relationships with colleagues regardless of job level or function
• Ability to navigate a constantly evolving scientific and regulatory environment, and approach challenges with a proactive, ownership mindset
• Direct experience hosting HealthAuthority inspections
• Demonstrated ability to mentor staff and build an effective Quality team
• Self-awareness, integrity, judgment, and ability to remain calm and consistent under pressure
• Role model for Quality mindset, as well as the CRISPR CUREsvalues (Collaboration, Undaunted, Results Oriented, Entrepreneurial)
• Ability to execute and follow-through to completion.
• Strong leadership and an innate ability to collaborate and build relationships is critical.

Preferred Qualifications

• Prior experience in the manufacture of cell and gene therapy products
• Progressive Quality Control and/or Analytical Sciences experience, including method transfer, validation and routine release and stability testing operations
• Advanced degree such as PhD in Life Sciences or a related field

Competencies

• Collaborative – Openness, One Team
• Undaunted – Fearless, Can-do attitude
• Results Orientation – Delivering progress toward our mission. Sense of urgency in solving problems.
• Entrepreneurial Spirit – Proactive. Ownership mindset.

Due to the nature of their work, our manufacturing and lab-based positions are located fully on-site.

Quality Site Head: Base pay range of $230,000 to $250,000+ bonus, equity and benefits

The range provided is CRISPR Therapeutics’ reasonable estimate of the base compensation for this role. The actual amount will be based on job-related and non-discriminatory factors such as experience, training, skills, and abilities.

CRISPR Therapeutics, Inc. is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law.

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