Senior Manager, Manufacturing Technical Services

Vertex Pharmaceuticals LLC; Boston (MA); On-site; USD 142,000 - 213,000; Full time

Job summary

The Senior Manager, Manufacturing Technical Operations (MTO) at Vertex Pharmaceuticals in Boston leads the quality-record program for CGT manufacturing, overseeing CAPAs, change controls, deviations, and investigations to ensure compliant, timely closures.

Reporting to Manufacturing and Quality Assurance, you will manage a team of five+, drive cross-functional collaboration, and focus on data-driven improvements, inspection readiness, and scalable quality-event practices on-site, including

Qualifications

• Bachelor's degree in engineering, Life Sciences, or related technical discipline.
• 6+ years of biopharmaceutical manufacturing, quality, or process development experience.
• 2+ years mentoring, supervising, or managing staff.
• Experience leading complex investigations, CAPAs, deviations, and change controls in GMP environments.
• Cell and gene therapy manufacturing experience is preferred.

Responsibilities

• Lead and develop a high-performing team for quality-record execution, including change controls, CAPAs, deviations, and investigations.
• Provide strategic oversight for CAPA and change-control records.
• Lead cross-functional investigations to determine root cause and actions.
• Establish best practices to advance quality-event center-of-excellence.
• Monitor performance metrics and data trends to prioritize work and allocate resources.
• Support inspection readiness and compliant documentation.

Skills

cGMP knowledge

GMP regulatory understanding

Project management

Analytical thinking

Communication skills

Leadership

Education

Bachelor's degree in engineering, Life Sciences, or related technical discipline

Job description

General Summary

The Senior Manager, Manufacturing Technical Operations (MTO), is responsible for developing and executing the quality-record strategy for quality events supporting internal Cell and Gene Therapy (CGT) manufacturing. The role provides end-to-end oversight of quality events, including corrective and preventive actions (CAPAs), change controls, deviations, and analytical investigations. Responsibilities include reviewing quality metrics and trends; escalating cross-functional risks and issues; and establishing operational excellence practices that strengthen quality event compliance, investigation quality, timely record closure, and the sustainable implementation of CAPAs and change controls. The Senior Manager partners closely with Manufacturing, Quality Assurance, and other cross-functional stakeholders to promote a quality event center of excellence and support continuous improvement across the site. This is an on-site position at the Boston site that requires 2nd shift/weekend availability to support manufacturing business needs.

Key Duties and Responsibilities

• Lead and develop a high-performing team of five or more responsible for quality-record execution, including change controls, CAPAs, deviations, and analytical investigations
• Provide strategic oversight and project leadership for complex, high-impact CAPA and change-control records
• Lead cross-functional investigations for major and critical deviations to determine root cause, define appropriate corrective and preventive actions, and present findings and recommendations to the leadership team for endorsement
• Establish, implement, and continuously promote MTO- and QA-aligned best practices to advance quality-event center-of-excellence capabilities
• Lead triage and proposal meetings for deviations, analytical investigations, CAPAs, and change controls
• Monitor quality-event performance, including compliance metrics, record-aging data, and recurring trends, to identify risks, prioritize work, and allocate resources using data-driven decisions
• Drive continuous improvement of departmental and site practices, procedures, systems, and activities related to quality-event management.
• Partner with cross-functional stakeholders to ensure timely, compliant, and effective closure of quality records
• Support inspection readiness by ensuring quality-event documentation is complete, scientifically sound, and aligned with applicable GMP requirements
• Perform other duties and lead additional projects as needed to meet departmental and business requirements

Knowledge and Skills

• In-depth knowledge of the conceptual and practical application of current Good Manufacturing Practices (cGMPs) within a pharmaceutical or biopharmaceutical manufacturing environment
• Strong understanding of global GMP requirements and quality-system expectations supporting GMP manufacturing
• Demonstrated experience managing complex projects, priorities, timelines, and cross-functional stakeholders
• Strong analytical and problem-solving skills, including the ability to evaluate trends, identify systemic issues, and implement sustainable improvements
• Excellent verbal and written communication skills, with the ability to tailor messaging, terminology, and level of detail to the intended audience
• Strong leadership skills and a demonstrated ability to collaborate, influence, and build productive relationships across functions
• Excellent planning, prioritization, and organizational skills, with the ability to balance production, development, compliance, and continuous-improvement needs

Education and Experience

• Bachelor's degree in engineering, Life Sciences, or a related technical discipline; equivalent combinations of education and relevant experience may be considered
• 6+ years of experience in biopharmaceutical manufacturing, quality, manufacturing sciences, process engineering, or process development
• 2+ years of experience mentoring, supervising, or managing staff
• Experience supporting GMP manufacturing environments and leading complex investigations, CAPAs, deviations, and/or change controls is preferred
• Experience in cell and gene therapy manufacturing is preferred

At Vertex, we embrace continuous learning and encourage employees to stay informed on advances in AI, technology, automation, and industry trends. We seek talent who bring an external perspective, demonstrate curiosity and sound judgment, and thoughtfully adopt new capabilities that improve decision-making, drive innovation, increase efficiency, and help deliver better outcomes for patients.

Pay Range

$142,000 - $213,000

Disclosure Statement

The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of facto