Location
Boston, MA
Compensation
$148k–$222k USD
Market range · company + function + seniority
p25 · target · p75 · n=12
Posted $222k · below the band
Tailor your résumé to this role in 30 seconds.
Free account · ATS keyword check · per-job bullet rewrite by Claude.
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
Requires 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 ability 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, communication, and coaching/influencing skills
Proven ability 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 - $222,000Disclosure 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 EligibleFlex 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 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
More open roles at Vertex Pharmaceuticals
Hiring velocity, headcount trend, and every open posting on one page.
Open postings ranked by description similarity — useful if this role isn't quite right.