Senior Manager, Manufacturing Technical Services

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

Benefits offered by this job

Annual bonus

Annual equity awards

Medical, dental, and vision benefits

Paid time off

Job summary

Vertex Pharmaceuticals is seeking a Senior Manager, Manufacturing Technical Operations (MTO) to own the quality-record strategy for CGT manufacturing. This on-site Boston role oversees CAPAs, change controls, deviations, and analytical investigations, driving improvements across quality-event management with cross-functional collaboration.

The position requires 2nd shift/weekend availability and leadership of a team; 6+ years in biopharma manufacturing and strong cGMP knowledge are essential.

Qualifications

• 6+ years of experience in biopharmaceutical manufacturing, quality, manufacturing sciences, process engineering, or process development.
• 2+ years mentoring, supervising, or managing staff.
• Experience supporting GMP manufacturing environments and leading complex investigations, CAPAs, deviations, and/or change controls is preferred.

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 corrective and preventive actions, and present findings to leadership.
• Establish and promote MTO- and QA-aligned best practices to advance quality-event center-of-excellence capabilities.
• Drive continuous improvement of quality-event management practices, systems, and activities.
• Partner with cross-functional stakeholders to ensure timely closure of quality records and inspection readiness.

Skills

cGMP knowledge

Quality-event management

Cross-functional leadership

Data analysis

Verbal and written communication

Project 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.

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 factors, including skills, competencies, experience, and other job-related factors permitted by law.

At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.

Flex Designation

On-Site Designated

Flex Eligibility Status

In this On-Site designated role, you will work five days per week on-site with ad hoc flexibility.

Note: The Flex status for this position is subject to Vertex’s Policy on Flex @ Vertex Program and may be changed at any time.

Company Information

Vertex is a global biotechnology company that invests in scientific innovation.

Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at [e-mail]