Senior Manager, CGP Compliance & Issue Management (Hybrid)

Reposted 11 Hours Ago
Be an Early Applicant
Boston, MA, USA
In-Office
138K-207K Annually
Senior level
Biotech • Pharmaceutical
The Role
The Senior Manager is responsible for compliance oversight, managing investigations, root cause analysis, and implementing CAPAs while ensuring adherence to GCP standards.
Summary Generated by Built In

Job Description

GENERAL POSITION SUMMARY:

The Senior Manager, RDQ Compliance is responsible for leading quality assurance and compliance activities in support of Compliance and Issues Management. This role requires expertise in overseeing investigations, root cause analysis, CAPA development, and effectiveness checks, as well as the ability to educate and guide stakeholders in performing effective root cause investigations. The ideal candidate will have experience in linking issues and risks, conducting data analysis, performing spot checks, and leveraging data trending to identify patterns and drive continuous improvement. This individual will work closely with Quality Leads, Study Team members, and other stakeholders while exemplifying Vertex Core Values.

RESPONSIBILITIES:

  • Quality Oversight and Monitoring:
    • Conduct regular spot checks to ensure adherence to GCP (Good Clinical Practice) standards and compliance with established processes.
    • Perform data trending and analysis to identify recurring issues, emerging risks, and opportunities for process improvement.
    • Monitor and evaluate key performance indicators (KPIs) to assess the effectiveness of quality and compliance activities.
  • Issue Management and Investigations:
    • Oversee internal and external GCP Quality Events, including but not limited to investigations, CAPAs, root cause analysis, and effectiveness checks.
    • Perform initial triage of event criticality in collaboration with Quality or Program Leads, Event Owners and other Subject Matter Experts (SMEs).
    • Escalate critical and major findings to Quality management and ensure timely resolution.
    • Oversee and provide guidance on root cause investigations, ensuring they are thorough, well-documented, and address the underlying issues.
    • Educate and mentor stakeholders on best practices for conducting effective root cause analysis to improve investigation quality and outcomes.
  • Corrective and Preventive Actions (CAPAs):
    • Oversee the development, implementation, and monitoring of corrective and preventive actions to address identified issues.
    • Ensure CAPAs are aligned with root cause findings and monitor their effectiveness through regular reviews and effectiveness checks.
    • Assist in driving alignment on CAPAs and process updates.
  • Data Management and Reporting:
    • Generate metrics, KPIs, dashboards, and reports to provide insights into quality trends and compliance performance.
  • Collaboration and Communication:
    • Collaborate with Quality Leads, Program Leads, and business contacts to ensure alignment on quality and compliance objectives.
    • Communicate proactively with internal and external partners, as well as management, to provide updates and address concerns.
  • Inspection Readiness and Training:
    • Participate in inspection readiness and support activities, ensuring all documentation is accurate, complete, and readily accessible.
    • Assist with onboarding and ongoing training of team members to ensure consistent understanding and application of quality standards.
    • Provide training and education to stakeholders on effective root cause analysis techniques and tools to enhance investigation outcomes.
  • Process Improvement:
    • Participate in and lead process improvement initiatives related to Issue Management, leveraging insights from spot checks and data trending to drive enhancements.
    • Assist in additional Quality Assurance initiatives as applicable

REQUIRED KNOWLEDGE, SKILLS, AND COMPETENCIES

  • Experience successfully leading and overseeing event investigations, Root Cause Analysis and CAPA
  • Strong analytical skills to evaluate complex data sets, identify trends, and derive actionable insights to support quality assurance and compliance activities
  • Knowledge of current industry trends and ability to use the latest technologies
  • Highly organized with strong planning capabilities
  • Compliance and quality management experience
  • Strong communication, problem solving and critical thinking skills
  • Ability to work under minimal supervision
  • Experience with quality management applications such as Veeva preferred

EDUCATION AND EXPERIENCE:

  • Bachelor’s Degree and 6 years of relevant work experience or a combination of training and experience

#LI-hybrid

Pay Range:

$137,800 - $206,800

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 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 [email protected]

Skills Required

  • Bachelor's Degree and 6 years of relevant work experience
  • Experience successfully leading and overseeing event investigations, Root Cause Analysis and CAPA
  • Strong analytical skills to evaluate complex data sets
  • Compliance and quality management experience
  • Knowledge of current industry trends and ability to use the latest technologies

Vertex Pharmaceuticals Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Vertex Pharmaceuticals and has not been reviewed or approved by Vertex Pharmaceuticals.

  • Parental & Family Support Policies provide 12 weeks of 100% paid bonding leave for all U.S. parents with additional fully paid time for birth parents. Family-forming supports include adoption and surrogacy assistance, fertility options like IVF and egg cryopreservation, breast‑milk shipping, subsidized childcare, backup care, and a DCFSA match.
  • Leave & Time Off Breadth Time off includes roughly four weeks of vacation, 13 holidays, sick time, and two companywide shutdowns (summer and year‑end). Some roles also include flexible or unlimited time off and paid volunteer time.
  • Retirement Support Programs include a 401(k) plan with employer contributions and an employee stock purchase plan. Filings describe employer contributions occurring in company stock, supporting long‑term ownership.

Vertex Pharmaceuticals Insights

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The Company
HQ: Boston, MA
5,000 Employees
Year Founded: 1989

What We Do

Vertex is a global biotechnology company that invests in scientific innovation to create transformative medicines for people with serious and life-threatening diseases. We discovered and developed the first medicines to treat the underlying cause of cystic fibrosis (CF), a rare, life-threatening genetic disease. In addition to clinical development programs in CF, Vertex has more than a dozen ongoing research programs focused on the underlying mechanisms of other serious diseases. Founded in 1989 in Cambridge, Massachusetts, our corporate headquarters is now located in Boston’s Innovation District, and our international headquarters is in London, United Kingdom. We currently employ approximately 3,500 people in the United States, Europe, Canada, Australia and Latin America with nearly two-thirds of our staff dedicated to research and development. Vertex is consistently recognized as one of the industry’s top places to work by Science Magazine, The Boston Globe, Boston Business Journal and the San Diego Business Journal. Our research and medicines have also received esteemed recognitions, including the Robert J. Beall Therapeutics Development Award, the French Prix Galien and the British Pharmacological Society awards.

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