Supervisor, Process Development Engineering

Vertex Pharmaceuticals LLC; Boston (MA); On-site; USD 104,000 - 156,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Paid time off

Job summary

Vertex Pharmaceuticals Incorporated in Boston, MA is seeking a Media and Buffer Preparation Supervisor to lead daily media, buffer, and stock solution preparation for cell therapy manufacturing, ensuring GMP-ready execution and high-quality output.

This role will develop a strong, accountable team, partner with cross-functional groups to improve processes, support scale-up and automation, and drive continuous-improvement initiatives across manufacturing operations.

Qualifications

• 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.

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.

Skills

Media preparation

Buffer preparation

Stock solution preparation

GMP/GMP-ready operations

Team leadership

Lean principles

Cross-functional collaboration

Automation awareness

Education

BS in Biochemistry, Engineering, Biology or related

MS with 6 years of industry experience

Tools

Aseptic processing

Laboratory safety practices

Job description

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:

$104,000 - $156,000

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.

#LI-Onsite

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.