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Vertex

Associate Director, Regulatory CMC, Biologics

Salary$166k – $250k
LocationBoston, MA
Work modehybrid
Typefull-time
SeniorityDirector
Experience8+ yrs
EquityIncluded
Company size10,000+ people
First seenOct 7, 2026 · 4d ago
Verified live1d ago
At a glanceSummarised by Seekless from the posting.
Must have15
Advanced knowledge of global regulatory CMC requirements (FDA, EMA, ICH, Health Canada) for biologics
Strategic thinking and problem solving
Excellent communication skills
Ability to lead and influence cross-functional teams
Strong planning and prioritization skills
Ability to work in a global matrixed environment
Commitment to quality and compliance
Working knowledge of AI tools for regulatory document preparation and review
Experience with structured content and data-driven authoring
Ability to critically review AI-assisted outputs
Familiarity with digital submission and data integrity expectations
Ability to identify automation and AI opportunities
Bachelor's degree in Biology, Chemistry, Pharmacy, Regulatory Affairs, or related life science field
8+ years of experience in pharmaceutical or biotechnology industry with a focus on biologics
Experience leading CMC regulatory submissions and HA interactions for biologics
Nice to have3
Advanced degree
Experience with complex or multi-product strategies
May include people management responsibilities
Skills
AI tools for regulatory document preparation and review
automation and AI opportunities
Benefits
Health insurance
Dental
Vision
Paid time off
Educational assistance
Student loan repayment
Commuting subsidy
Charitable donations match
401(k)
Job Description
General Summary:
The Chemistry Manufacturing Controls (CMC) Associate Director leads and executes global regulatory CMC strategies across investigational and commercial products focusing on biologics. This role is accountable for authoring, reviewing, and delivering high-quality regulatory submissions, while serving as the primary CMC interface with Health Authorities. The role integrates advanced digital and AI-enabled approaches to enhance the quality, consistency, and efficiency of regulatory document preparation and review.
Key Duties and Responsibilities:
•
Leads preparation, review, and lifecycle management of CMC sections of global regulatory submissions for biologics (INDs/CTAs, NDAs/BLAs/MAAs)
•
Develops and drives global CMC regulatory strategies for assigned programs
•
Serves as primary regulatory CMC lead for Health Authority interactions
•
Provides regulatory guidance to cross-functional teams
•
Leads regulatory assessment of CMC changes, deviations, and investigations
•
Applies AI-enabled tools for authoring, review, and consistency checks
•
Drives structured content and data traceability approaches
•
Supports AI/digital capability development
•
Contributes to process improvements and innovation initiatives
•
Represents Regulatory CMC in governance forums
•
Stays abreast of and adopts emerging technologies, including AI, and maintains a continuous learning mindset to strengthen regulatory CMC’s decision-making and innovation.
•
Proactively remains up to date on advances in technology, AI, automation, competitive intelligence, and changes in the regulatory environment.
Knowledge and Skills:
•
Advanced knowledge of global regulatory CMC requirements (FDA, EMA, ICH, Health Canada) for biologics
•
Strategic thinking and problem solving
•
Excellent communication skills
•
Ability to lead and influence cross-functional teams
•
Strong planning and prioritization skills
•
Ability to work in a global matrixed environment
•
Commitment to quality and compliance
•
May include people management responsibilities
Digital & AI-Enabled Regulatory Capabilities
•
Working knowledge of AI tools for regulatory document preparation and review
•
Experience with structured content and data-driven authoring
•
Ability to critically review AI-assisted outputs
•
Familiarity with digital submission and data integrity expectations
•
Ability to identify automation and AI opportunities
Education and Experience:
•
Bachelor’s degree in Biology, Chemistry, Pharmacy, Regulatory Affairs, or related life science field (advanced degree preferred)
•
8+ years of experience in pharmaceutical or biotechnology industry with a focus on biologics
•
Experience leading CMC regulatory submissions and HA interactions for biologics
•
Experience with complex or multi-product strategies preferred
About the company
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:
$166,400 - $249,600
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.
Benefits
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:
Hybrid-Eligible Or On-Site Eligible
Flex Eligibility Status:
In this Hybrid-Eligible role, you can choose to be designated as:
1.
Hybrid: work remotely up to two days per week; or select
2.
On-Site: 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 [email protected]
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