Vertex Pharmaceuticals Inc (US) Posted September 8, 2026

Senior Director, Analytical Development, Testing and Lab Automation

Boston, United States Full time
Manufacturing & CMC Senior Director
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Vertex Pharmaceuticals Inc (US) is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Job Description

General Summary:

The Senior Director, Analytical Development is a senior leadership role within the Cell and Gene Therapy Analytical Development function and will be responsible for setting and driving the company’s analytical testing strategy, including manual and automated testing approaches, analytical operations, and implementation of automation capabilities. This leader will oversee teams focused on automation of assays, testing in support of process workstreams, and analytical operations such as reagent and assay control management.

The role will work closely with Manufacturing, Process Development, Regulatory, Quality, CMC, and external partners to generate high-quality data that informs strategy and decisions, while advancing next-generation analytical automation tools for characterization of cell, gene and biologic therapy processes and products. This position will also shape broader analytical strategy across multiple programs and build organizational capability through strong scientific and people leadership.

Key Duties and Responsibilities:

Provide strategic leadership for the Testing, Operations, and Automation Analytical Development function across multiple programs

Establish and drive testing strategies using manual and automated methods to support process development, process characterization, and stability studies to build process/product understanding and inform control strategies (~70% of team resources)

Lead and oversee teams responsible for the development, optimization, and qualification of automated and PAT analytical methods and end-to-end automation platforms for process development and analytics (~20% of team resources)

Lead the establishment of laboratory informatics for highly automated equipment and digitization projects supporting data trending and visualization platforms that support interpretation of analytical datasets, including AI and machine learning tools. (~5% of team resources)

Establish and manage critical assay reagents, assay controls, and control charts to ensure optimal assay performance (~5% of team resources)

Set and reinforce operational best practices across analytical development, including sample management, data management, data integrity, documentation in notebooks and reports, and training

Build strong cross-functional and external partnerships to advance analytical and program goals

Author and review technical and scientific documents, including presentations, study protocols, reports, and test methods

Recruit, mentor, and develop organizational talent while managing department resources, budget, and headcount

Knowledge and Skills:

Extensive experience establishing and leading analytical testing teams, including establishment of testing strategies that include manual and automated methods

In-depth experience and aptitude in laboratory informatics and implementation of AI/machine learning tools for laboratory automation, partnering with Digital/IT functions

In-depth experience with automation of analytical method development, optimization, and qualification and end-to-end automation platforms supporting process development and analytics

In-depth experience with digitization projects including data trending and visualization platforms to support interpretation of datasets

Knowledge of product characterization testing and analytical procedure implementation. Experience supporting PAT method development, process development, process characterization, and stability studies

Expertise in sample management, data management, and data integrity practices

Experience managing critical assay reagents, assay controls, and control charts

Strong understanding of ICH, FDA, and USP guidelines, and ability to apply them in the context of pharmaceutical development stage

Experience authoring and reviewing study protocols, reports, test methods, and regulatory-supporting documentation

The following capabilities are especially important for success in this role:

Self-driven and recognized as a laboratory digitization champion

Proven track record of people leadership and managing high throughput testing

Ability to lead in a fast-paced environment, manage competing priorities, and maintain timelines across multiple activities

Strong scientific depth within one’s discipline, with a broad understanding of adjacent scientific disciplines and the drug development process

Excellent written, verbal, interpersonal, and matrix leadership skills

Ability to influence internal and external stakeholders and work effectively both independently and in team environments

Scientific leadership marked by high ethical standards and broad peer respect

Extensive experience establishing and leading analytical testing teams, including establishment of testing strategies that include manual and automated methods

Education and Experience:

Masters degree or PhD in relevant discipline (analytical chemistry, immunology, biochemistry, cell biology, biotechnology or related field) with progressive experience in technical leadership roles in the pharmaceutical industry. Experience with Cell Therapy, Biologics, and Genetic therapies is critical

Ph.D. (or equivalent degree) and 11+ years of relevant post-doctoral employment experience, or

Masters Degree (or equivalent degree) and 15+ years of relevant employment experience

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:

$226,100 - $339,100

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.

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

Job details

Seniority
Senior Director
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Boston, United States
Employment type
Full time

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 119 comparable Senior Director Manufacturing & CMC roles across 45 biopharma companies.

119Comparable roles tracked
117Currently active
45Companies hiring similar roles
13Countries represented

Salary context

66 of 119 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject $226,100/yr – $339,100/yr
Lowest disclosed · Director - Engineering Design Lead · Lilly $130,500/yr – $191,400/yr
Highest disclosed · Executive Director, CMC Regulatory Science · ModernaTX, Inc. $224,900/yr – $404,600/yr
Peer group range $160,950 – $314,750 (median $222,200)

Where these roles are based

Top locations among the 119 comparable roles

United States83
Ireland9
Netherlands7
India5
United Kingdom4
China3

+ 7 more countries

Seniority mix

119 of 119 peers have a known seniority level

Director82
Senior Director30
Executive/VP7

Therapeutic area mix

1 of 119 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Lilly Indianapolis, Indiana, United States of America Senior Director
Same function Same seniority Same country
60%similar
Regeneron Pharmaceuticals, Inc (USA) Renss, United States Senior Director
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60%similar
Amgen Inc. Thousand Oaks, United States Senior Director
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60%similar
Lilly Concord, North Carolina, United States of America Senior Director
Same function Same seniority Same country
60%similar
Lilly Huntsville, Alabama, United States of America Senior Director
Same function Same seniority Same country
60%similar
Lilly Huntsville, Alabama, United States of America Senior Director
Same function Same seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
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Lilly · Indianapolis, Indiana, United States of America · Senior Director
Function Therapeutic area Seniority Country
60%
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Gilead Sciences, Inc. · Foster City, United States · Senior Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.