Associate Director, Quality Systems - Cell and Gene Therapies (VCGT)

About this role

Job Description Position Summary The Quality Systems Associate Director supports strategic   design   of   and ensures tactical execution of quality systems, risk management, and quality culture across the Vertex Cell and Gene Therapy (VCGT) organization.   The role   is responsible for   partnering with cross-functional technical development and commercial teams to align and   facilitate   harmonization of strategy, procedures and processes related to the Quality Management System and to drive Quality improvements.  

This position reports directly to the Director of Quality.  

Key Duties & Responsibilities The responsibilities of this position may include, but are not limited to, the following:

-Process Lead for Annual Product Quality Review (APQR) and Quarterly Product Quality Assessment (QPQA) including:  

• Responsible for leading and providing functional process oversight for APQR and QPQA  

• Ensure all APQR and QPQA are executed on time and   in accordance with   procedures and regulatory requirements  

• Monitor and support the quality risk   management   program items associated with CGT .    Identify   and implement continuous improvement projects to improve processes and make them efficient and scalable  

-Process Lead for VCGT Data Integrity (DI) program  

• Define DI compliance   operational   strategies   to be   deployed   at the local site level   and   monitored   for effectiveness, including governance  

• Collaborate with Global Process owner to   identify   and implement DI continuous improvement projects to mature processes and make them efficient and scalable  

• Responsible for local Quality system oversight, metrics, and improvement including change control, events, CAPA, escalation, and risk management  

• Leads the monitoring, interpretation, and communication of QMS processes and metrics requirements including remediation plans  

• Collaborates with internal and external business partners to resolve complex quality issues to ensure compliant solutions  

• Provide hands-on   expertise   in the   day-to-day   management of data collection systems and control within the   GxP   Quality Management System using digital solutions  

• Responsible for strategic, Risk Management monitoring support, and Data Integrity initiatives and activities to drive prioritization and in-support continuous improvement across VCGT QMS/Compliance processes   

• Supports internal audit or external audit programs  

• Works to enhance Quality Culture across VCGT organization  

• Provides Project Management leadership for department projects/initiatives.  

Required Education Level • Bachelor's degree in a scientific discipline, operations research, operations management, business administration or a related field

Required Experience • R equires 10 +   years of experience or the equivalent combination of education and experience  

• Experience in product life cycle from discovery to commercial product development  

Required Knowledge/Skills • Broad and deep   expertise   in global GMP regulations,   guidances , and Quality Management Systems, as well as a strong understanding of industry standards and best practices across the   GxP   lifecycle  

• Strong leadership skills with a bility to be agile and effectively collaborate in a dynamic, cross-functional matrix environment  

• Ability to assess impact across multiple procedures and systems  

• Ability to lead and manage complex projects/teams within corporate   objectives   and project timelines  

• Proficiency   utilizing   project management processes / tools to lead meetings,   assist   with project planning and   facilitate   completion of tasks  

• Excellent technical writing,   presentation   and communication skills  

• Ability to effectively influence others within technical area of expertise  

• Outstanding facilitation,   c ommunication, and   c oaching/influencing skills  

• Proven   a bility to lead improvement projects and project teams  

• Ability to navigate through ambiguity and rapid growth and adapt to change  

• Proven ability to   identify   and analyze performance indicators.    

• Extensive experience conducting investigations, performing root cause   analysis   and   identifying   CAPA  

Other Requirements Up to 15% travel

Pay Range: $148,000 - $222,000 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: 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. 

#LI-Hybrid  

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 empl

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