Manager, Quality Assurance Operations

Genetix Biotherapeutics; Boston (MA); Hybrid; USD 118,000 - 166,000; Full time

Benefits offered by this job

Health insurance

401(k) plan

Tuition reimbursement

Paid holidays

Paid parental leave

Commuter subsidy

Job summary

Genetix Biotherapeutics in Somerville, MA is seeking a Manager, Quality Assurance Operations to provide end-to-end QA oversight of CMOs and ensure cGMP compliance. You will partner with Manufacturing, MS&T, QC, and Patient Supply to drive risk management and change controls.

You will lead QA governance forums, review quality systems, manage Deviations and Change Controls, and maintain CMO Quality Agreements. This hybrid role requires strong leadership in a fast-paced biopharma environment.

Qualifications

• Bachelor’s degree in Life Sciences, Engineering, or related discipline (advanced degree preferred).
• 7+ years of experience in Quality Assurance within GMP-regulated biopharmaceutical or cell/gene therapy manufacturing.
• Strong experience supporting CMO oversight and external manufacturing environments.

Responsibilities

• Provide on-call QA support for manufacturing operations and manage quality events.
• Lead QA governance forums and joint governance meetings with CMOs.
• Review and approve Deviations and Change Controls; manage investigations.

Skills

QA Oversight

Cross-functional leadership

Risk-based decision making

Communication

Matrix environment

Education

Bachelor’s degree in Life Sciences/Engineering

7+ years QA GMP experience

Tools

Change Control systems

Deviation management

Investigation processes

Job description

About Genetix Biotherapeutics

At Genetix Biotherapeutics every role has meaning, every team member is respected, and every day is a chance to make a difference. When you join Genetix, you're not just landing a new role, you become part of a company that's pursuing curative gene therapies to give patients and their families more days. We are doers, thinkers and collaborators who embrace and live by our values:

At Genetix Biotherapeutics every role has meaning, every team member is respected, and every day is a chance to make a difference. When you join Genetix, you're not just landing a new role, you become part of a company that's pursuing curative gene therapies to give patients and their families more days. We are doers, thinkers and collaborators who embrace and live by our values: Our innovation is rooted in the diversity of our teams and results are achieved through cooperation and the integration of multiple viewpoints. This is personal and we approach every challenge with radical care.

Summary

The ‘Manager, Quality Assurance Operations’ role is responsible for providing end-to-end quality oversight of Contract Manufacturing Organizations (CMOs) to ensure compliance with cGMP regulations, regulatory commitments, and Genetix quality standards. This role serves as a key quality partner to Manufacturing, MS&T, Quality Control, and Patient Supply. The role is expected to serve as a CMO Lead point-of-contact and primary quality interface with external partners, driving proactive risk management, and Deviation and Change Control lifecycle management. The position ensures effective quality oversight through structured governance forums, review and approval of quality systems, and continuous monitoring of performance metrics. This is a full-time hybrid position (3 days a week) in our Somerville – Assembly Row, Massachusetts office.

Responsibilities

• Provide on-call QA support for manufacturing operations, ensuring proactive identification, escalation, and mitigation of quality events and risks impacting ongoing manufacturing and product disposition
• Maintain a consistent and effective external oversight model, including leading QA-to-QA forums and guiding quality discussions in joint governance meetings with CMOs.
• Lead regular internal Deviation/Lab Investigation Management meetings, ensuring compliance, quality, and timeliness.
• Review and Approve internal and external CMO Deviations and Change Controls
• Serve as QA point-of-contact for Product Complaints, ensuring appropriate investigation, documentation, and closure.
• Perform Quality Impact Assessments for Change Controls, ensuring appropriate risk evaluation and mitigation.
• Represent Quality Assurance Operations in Manufacturing Tier meetings, ensuring alignment on quality risks, priorities, and escalation pathways.
• Represent Quality Assurance Operations in Change Control Review Board (CCRB) meetings.
• Serve as QA reviewer and approver for: process validation protocols and reports, technical reports and supporting documentation, and internal and external validation deliverables
• Monitor CMO quality performance metrics, identify trends, and drive continuous improvement initiatives.
• Own and manage CMO Quality Agreements, including authoring, reviewing, negotiating, and maintaining compliance with current regulatory expectations.
• Author and review Annual Product Quality Reviews (APQRs) to ensure comprehensive evaluation of product and process performance.
• Identify trends, risks, and opportunities for improvement across the product lifecycle.

Required Education, Experience, or Qualifications (or equivalent)

Education & Experience

• Bachelor’s degree in Life Sciences, Engineering, or related discipline (advanced degree preferred)
• 7+ years of experience in Quality Assurance within GMP-regulated biopharmaceutical or cell/gene therapy manufacturing
• Strong experience supporting CMO oversight and external manufacturing environments

Technical Skills

• Deep knowledge of: cGMP regulations (FDA, EMA, ICH guidelines), Deviation, CAPA, and investigation processes, Change Control systems and validation lifecycle
• Knowledge of lentiviral vector process preferred
• Knowledge of process validation preferred
• Strong understanding of cell/gene therapy manufacturing or biologics

Leadership & Competencies

• Demonstrated ability to lead cross-functional quality governance forums
• Strong risk-based decision-making and escalation capabilities
• Excellent communication, stakeholder management, and influential skills in internal and external settings
• Ability to operate effectively in a fast-paced, matrixed CMO environment
• High attention to detail with an inspection-ready mindset

Key Success Factors

• Proactive risk identification and escalation during manufacturing operations
• Timely closure and high-quality management of deviations and investigations
• Strong, compliant oversight of CMO operations and quality systems
• Effective cross-functional collaboration and governance leadership
• Continuous improvement of quality systems and performance metrics

Additional Information

This pay transparency range provided below is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. We may ultimately pay more or less than the posted range, and the range may be modified in the future. This role is eligible for an annual bonus and long-term incentive. Actual base salary pay will be based on several factors, including but not limited to experience, skills, relevant education/qualifications, external market, internal equity, and other job-related factors permitted by law. Genetix’s total rewards package also provides employees with a comprehensive and competitive benefits suite to support a variety of employee needs. These benefits include comprehensive health, life and disability insurance, employer-matched 401(k) plan, lifestyle spending account, flexible time‑off + paid holidays and winter holiday period, tuition reimbursement & loan repayment assistance, paid parental leave, paid onsite parking, commuter subsidy, and much more.

Pay Transparency: $118,000 USD - $166,000 USD

Equal Opportunity Employer

Genetix is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status or any other applicable legally protected characteristics.