Job Description

General Summary:

The Associate Director is responsible for managing the operations of Vertex’s external commercial network which includes Drug Substance, Drug Product Intermediate and Drug Product manufacturing, working in the External Manufacturing Operations team. Managing the external manufacturing network is a critical component of the Commercial Manufacturing and Supply Chain team’s role in ensuring that the company effectively and efficiently delivers medicines to patients. The Associate Director provides vision, leadership, and both strategic and enterprise thinking in the management of the external partners. This leader will also cultivate and leverage multiple cross-functional business relationships to identify and execute creative solutions to organizational opportunities and challenges. The Associate Director of External Manufacturing reports directly to the Senior Director, External Manufacturing. This position will be based in Vertex’s corporate headquarters in Boston, MA. This role will be accountable for a specific CDMOs external commercial manufacturing operations activities across all phases for small molecules. This role will partner closely with colleagues across Vertex to ensure seamless supply of all commercial products manufactured at the CDMO. The candidate will be in a hybrid role (3 days/week onsite), with travel to CDMO sites, as necessary.

Key Duties and Responsibilities:

• Acts as main point of contact for CDMO(s) including leader of CDMO working teams and strategic business review chairperson.
• Responsible for Long Term Strategic supplier management and accountable for Supplier Relationship Management (SRM) and SRM related processes for given CDMOs.
• Responsible for driving execution of commercial production plans: Provide operational oversight and troubleshooting support to ensure all deliverables meet or exceed Vertex requirements (including but not limited to successful execution of manufacturing operations, on-time shipments, quality compliance and cost management).
• Responsible for driving execution of the production plan at CDMO. (PO through delivery).
• Partners with MS&T, Quality and CMSC Strategy and Business Operations to champion a culture of quality with our CDMO’s and to ensure that all activities and documentation comply with regulatory requirements.
• Establish a robust tracking and reporting process to monitor CDMO performance using a set of standard KPIs (Key Performance Indicators) and report progress to management.
• Leads identification and resolution of business/contract issues (bring in legal, CMSC LT, Strategy +Bus Ops, Strategic Sourcing)
• Partners with Vendor Management, Strategic Sourcing and Strategy and Business Operations to further develop our Supplier Relationship Management and Supplier Contracting Programs.
• Partners with Global Supply Chain to develop long-term manufacturing network strategy and to maintain a flexible, reliable, robust, and cost-effective manufacturing network.
• Champions a strong winning culture, fostering teamwork and commitment to excellence through transparent communication.
• Ability to travel, international, up to 40%.

Knowledge and Skills:

• Understanding of the science and technology underlying small molecule manufacturing as well as analytical techniques that support commercial manufacturing activities.
• Demonstrated understanding of the principles and applications associated with commercial manufacturing operations, maintenance, and engineering.
• Strong knowledge of cGMP requirements.
• A strategic thinker with strong result-orientation and a sense of urgency to deliver quality results on time and in a highly ethical and professional manner.
• Understanding of the technical aspects of manufacturing, testing, and controls, the regulations governing pharmaceutical operations, as well as financial systems and controls.
• Excellent communication and interpersonal skills with the ability to work in strong cross-functional relationships and communicate complex issues and concepts enterprise-wide, from the executive team to the manufacturing floor.
• Excellent team player and be able to build and sustain organization respect and trust at all levels.
• Problem solver with a hands-on approach and ability to anticipate adverse scenarios and provide contingency plans to address them.
• Resilient and able to work well in a demanding, fast-paced entrepreneurial environment.
• Sound judgment and business acumen with personal versatility and flexibility as business and team evolve.
• Keeps current on professional knowledge, expertise and best practices.

Education and Experience:

• BS or MS or PhD in Chemical Engineering, Chemistry or related discipline
• BS and 8+ years of experience (6+ years with Masters, 4+ years with PhD)
• Previous experience working on process development, optimization and commercialization of drug substance and drug product

Pay Range:

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:

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 ApplicationAssistance@vrtx.com