Vertex Pharmaceuticals
Manager, Manufacturing Operations (2nd Shift)
Boston, MA · Mid
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Green-card filing pattern in this occupation
Green-card follow-through: 83%
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About the role
- This role is responsible for defining and directing activities for cell therapy and cell therapy personnel while maintaining organizational balance across the group.
- This position is accountable for safe, compliant, and efficient cGMP operations, including equipment setup, assembly, operation, disassembly, and cleaning, while providing leadership to supervisors and manufacturing staff.
- Direct the activities of the group through management of staff, prioritization, and assignment of tasks.
Responsibilities
- Lead and manage daily manufacturing operations.
- Provide leadership, direction, and support to Manufacturing Supervisors and frontline manufacturing personnel.
- Ensure accurate execution, authoring, review, and approval of batch documentation to maintain compliant manufacturing records.
- Partner with cross-functional teams to support facility operations, maintenance activities, investigations, deviations, change controls, and manufacturing objectives.
- Maintain the facility in an audit-ready state through adherence to procedures, documentation practices, and inspection readiness standards.
- Ensure compliance with SOPs, policies, and work instructions to support safe and successful facility operation.
Requirements
- Experience in pharmaceutical manufacturing operations within a cGMP-regulated environment required.
Skills
- Strong interpersonal, communication, and organizational skills.
- Sound understanding of relevant drug development and manufacturing activities, including applicable standard operating procedures (SOPs).
- Ability to clearly communicate rationale for procedures, practices, and technical approaches.
- Demonstrated competency in the principles and practice of cGMPs and associated regulatory considerations in a pharmaceutical environment.
- Solid understanding of process, equipment, and facility validation requirements.
- Solid understanding of the cGMP framework in both development and commercial pharmaceutical drug product manufacturing environments.
- Working knowledge of inspection readiness, deviation management, CAPA, change control, and continuous improvement practices.
- Education and Experience:
- Bachelor's degree required, preferably in a scientific, technical, or engineering discipline.
- 4+ years of experience or the equivalent combination of education and experience.
- Prior people leadership experience required, including experience managing staff, supervisors, and/or manufacturing teams.
- Prior cell therapy and aseptic manufacturing experience preferred.
Compensation
- $119,900 - $179,900
- 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.
Company info
- At Vertex, we embrace continuous learning and encourage employees to stay informed on advances in AI, technology, automation, and industry trends.
Equal opportunity
- 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 ApplicationAssistance@vrtx.com
This listing is sourced directly from Vertex Pharmaceuticals's careers page and normalized into a canonical job model.