Supervisor, Process Development Engineering

Job Description

General Summary

Vertex is seeking a Media and Buffer Preparation Supervisor to support media development and cell therapy manufacturing activities in Boston, MA. This role leads daily media, buffer, and stock solution preparation operations; ensures reliable, high-quality, and GMP-ready execution; and develops a strong, accountable team. The Supervisor will partner with cross-functional teams to improve processes, support scale-up and manufacturing readiness, and advance automation and continuous-improvement initiatives.

Key Duties and Responsibilities

• Supervise daily media, buffer, and stock solution preparation, including scheduling, prioritization, troubleshooting, and escalation of issues.
• Lead, coach, train, and develop team members to strengthen technical skills, accountability, and operational discipline.
• Ensure consistent, accurate, and high-quality output by following standard work, procedures, and quality requirements.
• Plan staffing and resources to meet customer needs and maintain reliable operations.
• Partner with cross-functional teams to support operational readiness, scalable manufacturing practices, and business priorities.
• Drive continuous improvement, lean initiatives, and automation solutions to improve efficiency, scalability, and data visibility.
• Maintain GMP/GMP-ready compliance, safety, documentation, investigations, CAPAs, and a collaborative team environment.

Knowledge and Skills

• Knowledge of media, buffer, and stock solution preparation in laboratory, pilot-scale, or biopharmaceutical manufacturing settings.
• Understanding of GMP/GMP-ready operations, including documentation, data integrity, deviations, change controls, and CAPAs.
• Working knowledge of aseptic processing, cell culture support, scale-up, and laboratory safety practices.
• Ability to lead daily operations, including work prioritization, scheduling, troubleshooting, and escalation management.
• Demonstrated people-leadership skills, including coaching, training, development, and accountability.
• Strong problem-solving and continuous-improvement skills, including lean principles, waste reduction, and process optimization.
• Strong organizational, communication, and cross-functional collaboration skills.
• Preferred: Experience with cell or gene therapy manufacturing, technology transfer, automation, digital manufacturing systems, and Industry 4.0 tools.

Education and experience

• BS in Biochemistry, Engineering, Biology or related discipline with 7 years of industry experience or an MS with 6  years of industry experience.
• Practical industry experience in media preparation, stock solution preparation, manufacturing support, or related biopharmaceutical operations.
• Experience leading day-to-day operations in a laboratory, pilot-scale, or manufacturing support setting.
• Hands-on leadership experience with training, scheduling, troubleshooting, and team accountability.

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:

Disclosure Statement:

Flex Designation:

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.

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