Director, Drug Product Process Development - Biologics

Job Description

Biologics, Cell and Gene Therapy is a rapidly growing part of Vertex Pharmaceuticals where research, development, and clinical manufacturing are highly integrated together at our new R&D site in Boston Seaport.

General Summary

Vertex is seeking a highly skilled technical leader to join our Process Development / Engineering team to lead the development and manufacturing of biologics drug products for our growing pipeline. The Vertex Process Development team offers a dynamic, fast-paced, and highly collaborative environment with a tremendous impact on our programs and for our patients. Our team focuses on bringing together the best process design, scale‑up and cutting‑edge manufacturing technologies to enable the successful implementation of Biologics, Cell and Genetic therapeutics.

The successful candidate will lead the development and manufacturing of biologics drug products. The responsibilities include formulation development, primary container development, fill‑finish process development, technology transfer of manufacturing processes to CDMOs, and process validation to support our clinical pipeline toward commercialization. This is a highly cross‑functional role that will work closely with drug substance development, analytical development, device development and supply chain management in CMC teams to drive technical and strategic decision‑making.

Key Duties and Responsibilities

• Lead phase‑appropriate strategies for drug product development, process transfer, scale‑up and process characterization to support commercial readiness.
• Set‑up and oversee external capabilities for developability assessment and formulation screening for high‑concentration biologics, ADCs and other biologics modalities.
• Define and develop robust fill‑finish manufacturing processes for liquid and lyophilized drug products in vials, pre‑filled syringes and other novel primary packaging.
• Oversee drug product technology transfer, process development and GMP manufacturing operations at CDMOs.
• Define and develop clinical dose preparation and administration strategies for drug products for multiple indications. Collaborate with clinical and supply chain teams to prepare clinical study documentation.
• Collaborate with the device development team to develop combination product presentations such as pre‑filled syringes, autoinjectors and advance delivery technologies.
• Define and implement drug substance and drug product stability and shelf‑life assessment approaches.
• Develop and manage project timelines, resource allocation, and budget for drug product programs.
• Manage deviations and OOT / OOS investigations at the CDMOs in collaboration with Quality, External Manufacturing and Regulatory team.
• Define and implement control strategies, validation protocols, and process characterization studies in accordance with Quality by Design (QbD) principles.
• Author and review regulatory submissions : IND / IMPD, briefing books and BLA.
• Serve as a subject matter expert in regulatory agency interactions, audits, and inspections.
• Identify and implement innovative technologies and best practices to improve process robustness, efficiency, and compliance.
• Potential in the future to build and manage a team of scientists and engineers to deliver high‑quality, scalable, and compliant drug product processes from early development through commercialization.
• Expected travel : 10-20% (domestic and international).

Required Education

Required Experience and Skills

Pay Range

$195,500 - $293,200

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.

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.

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