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Vertex Pharmaceuticals
Boston, Massachusetts, United States
(on-site)
Posted
2 days ago
Vertex Pharmaceuticals
Boston, Massachusetts, United States
(on-site)
Job Type
Full-Time
Job Function
Other / Not Listed
Director, Analytical Development, Biologics
The insights provided are generated by AI and may contain inaccuracies. Please independently verify any critical information before relying on it.
Director, Analytical Development, Biologics
The insights provided are generated by AI and may contain inaccuracies. Please independently verify any critical information before relying on it.
Description
Job DescriptionGeneral Summary:
Vertex is seeking a talented and experienced leader to join our Analytical Development Team to lead CMC analytical development for Biologics. The experienced leader will play a central role in advancing our biologics portfolio by building analytical development strategies through a combined internal and external network. The individual is responsible for providing strategic and technical leadership for analytical development of biologics from the discovery interface to first license approval and beyond, such as post approval 2nd generation product development. The individual is expected to lead multiple analytical matrix team leaders, in defining and execution analytical development strategies with phase appropriate development approaches.
The successful candidate must work well in a fast-paced, integrated team environment. Strong experience in managing external CRO/CTO is a must. The individual is expected to drive effectively with external partners in the execution of analytical development activities for multiple programs. The candidate must demonstrate strong technical expertise in state-of art analytical methodologies and problem-solving skills. Strong technical background is desired in the area of analytical techniques commonly used in the analysis of biologics products, along with data analysis and statistics used in product specification setting.
The candidate is expected to collaborate closely with the Research, Process Development, Manufacturing, Quality, Regulatory functions to develop and deliver products to the clinical. The ability to work both independently and in a matrix team environment is essential. As a member of dynamic and diverse Analytical Development and CMC teams focused on science and innovation, this position will provide opportunities for continued learning and cross-functional collaboration enabling the individual to grow broadly beyond one's own discipline as a scientific and strategic leader.
Key Duties and Responsibilities:
- Leads analytical strategy development of biologics
- Partnering with internal and external labs in executing analytical development activities, including designing, planning, and executing all analytical activities that can lead to successful IND/IMPD and/or BLA/MAA applications.
- Authors CMC sections of regulatory submissions. Ensures that all regulated work and documents conform to GMP standards
- Proactive resource planning to align with established development strategy
- Planning budget proposals and manages execution of approved activities within budgets
- Maintain a strong internal and external network for the execution of analytical activities
- Mentoring a team of analytical matrix leaders. Remove roadblocks. Build strategy roadmaps in advancing technical leadership in biologics development
- 10% travel
Knowledge and Skills:
- Excellent communication skills and interpersonal skills with the ability to build strong cross-functional relationships and communicate complex issues and concepts
- Track-record in leading cross-functional matrix team
- Track record in developing analytical phase appropriate strategy for biologics development
- Excellent problem-solving skills in biologics development
- Deep technical understanding of analytical methodologies, such as LC, iCE, CE-SDS, ELISA, PCR, particulates etc.
- Deep technical expertise to lead analytical method validation and analytical transfer, establish analytical control strategy, design stability programs and comparability studies.
- Experience authoring CMC sections of regulatory documents.
- Experience of Regulatory guidelines relevant to biologics development
- Knowledge of cGMP requirements
- A strategic thinker with a strong result orientation and a sense of urgency to deliver quality results on time and in a highly ethical and professional manner
- The ability to work in a dynamic, fast pace, matrix environment, manage priorities and maintain timelines for multiple projects.
Education and Experience:
- 9+ years (PhD) or 12+ years (MS) in relevant discipline (analytical, biochemistry, molecular biology, biotechnology or related field) with progressive experience in technical leadership roles in the biotech industry, and specifically in the development of analytical control strategies. Experience with Biological products CMC development is critical.
#LI-BS1
Pay Range:
$197,500 - $296,200
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 ID: 80937700
At Vertex, we bring together the brightest minds in the relentless pursuit of creating transformative medicines for people with serious and life-threatening diseases. Founded in 1989 in Cambridge, Massachusetts, we are one of only a handful of biotechnology companies founded since 1976 that has discovered and developed four or more approved medicines in our own labs. In addition to the four medicines we’ve developed to treat the underlying cause of cystic fibrosis, we have ongoing research programs focused on the underlying ...
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