Vertex Pharmaceuticals
Director, Clinical Quality & Development Operations
Boston, MA · Director
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odds of building a lasting career here
Sponsors, but it's cap-subject — you still face the weighted lottery (~61% per draw at Level IV). Good if you win; have a cap-exempt backup on your list.
Lottery odds assume a STEM candidate.
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This range already reaches Level IV — the maximum four lottery entries.
DOL prevailing wage, 2026-27 wage year · Mechanical Engineers (17-2141) · Boston-Cambridge-Newton, MA-NH. Wage level is derived by USCIS from the offered wage, occupation and worksite; the occupation shown is inferred from the job title.
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Green-card follow-through: 83%
Files H-1B transfers
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About the role
- Defines and executes the overarching vision and strategy for Operational Excellence ensuring alignment with GCO and enterprise objectives.
- Provide leadership and coordination across all domains to ensure operational excellence and ensure timely delivery of all goals.
- Oversees strategic vendor relationships, including selection, performance monitoring, and risk mitigation for ancillary supplies, safety submissions, and training services.
Responsibilities
- Maintains inspection readiness and compliance within all domains and adherence to regulatory standards.
- Builds and maintains strong and productive relationships with key stakeholders within GCO, the Quality Organization, and LMS Organization influencing senior stakeholders and contributing to enterprise-level decision-making.
- Comprehensive understanding of own discipline concepts and principles in multiple disciplines and a broad knowledge of others. Oversees multiple projects within domain in support of CQDO deliverables and is a SME for their domain.
- Leverage knowledge of the potential future stakeholder landscape and to support the pipeline and identify those who will be the most influential, internal and external, to Vertex
- Drive the development of innovative solutions that address evolving business needs in line with standards
- Deep understanding of concepts and principles in own discipline. Basic knowledge of other disciplines. Responsible for managing technical tasks or assigned as a SME for more than one area.
Requirements
- Basic knowledge of other disciplines.
- Guided by policies and departmental plan, impacts the team's ability to achieve objectives.
- Bachelor of Science degree in a life sciences discipline
Skills
- Advanced understanding of GCP, CFR and ICH guidelines and Health Authority regulations
- Significant experience managing clinical quality activities and in-depth knowledge of clinical operations
- Demonstrated attention to detail, accuracy, excellent review and analytical skills in a fast-paced environment.
- Expert knowledge in system/technical tools and processes
- Results oriented
- Significant experience with line management of employee
- Excellent leadership and interpersonal skills with an ability to effectively work and problem solve within a multidisciplinary team
- Experience in collaborating and working with global and cross-functional teams
- Excellent oral and written communication skills to influence, inform, or guide others and to communicate complex concepts
- Demonstrated adaptability, flexibility, independence and resourcefulness to thrive in a mid-sized company environment
- Proven successful track record in maintaining knowledge and compliance of regulatory requirements
- Education and Experience:
Compensation
- $184,000 - $276,000
- 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.
Benefits
- Typically requires 10 years of experience, or the equivalent combination of education and experience, in the biopharmaceutical industry
- Provides strategic oversight for GCO-wide training programs, competency development, and continuous learning initiatives to build a high-performing workforce.
Company info
- work remotely five days per week and come into the office on occasion - you're always welcome on-site; or select
- work remotely up to two days per week; or select
- work five days per week on-site with ad hoc flexibility.
- 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 ApplicationAssistance@vrtx.com
This listing is sourced directly from Vertex Pharmaceuticals's careers page and normalized into a canonical job model.