Director, GDP Operational Quality (Hybrid)

Reposted 24 Days Ago
Be an Early Applicant
Boston, MA, USA
In-Office
182K-274K Annually
Expert/Leader
Biotech • Pharmaceutical
The Role
The Director of GDP Operational Quality oversees quality processes for distribution operations, ensuring compliance and continuous improvement, while leading a team and collaborating with internal and external stakeholders.
Summary Generated by Built In

Job Description

The Director, GDP Operational Quality is responsible to partner with Trade Operations to support the distribution of Vertex’s commercial product portfolio.  The role is responsible for oversight of team activities, development of personnel and ensuring timely completion and quality of deliverables/goals within their remit.   The role supports GDP quality operations for all distribution activities within the US; key stakeholders include Trade Operations, Vendor Quality Management & Quality Compliance.

Key Duties and Responsibilities:

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

  • Primary quality partner for Vertex US Trade Operations organization, providing quality input and perspective to US Trade Ops continuous improvement initiatives and projects

  • Accountable for ensuring US Trade Ops organisation are operating within the Vertex GDP Quality Management System, accountable to ensure deviations are investigated, recorded in the QMS and CAPAs are identified.

  • Establish robust Quality Processes/Process Ownership for the distribution of Vertex Commercial Finished Goods within the US

  • Responsible for local release activities required to support distribution of Vertex Commercial products

  • Support Trade Operations with Risk Management activities

  • Support the Shipping, Storage & Distribution (SS&D) Process Owners Network (PON).  Build, maintain and drive and manage PON activities set out in the SS&D Roadmap

  • Responsible for the Quality oversight and management of Vertex strategic US third party logistics providers : creating and maintaining Quality Agreements, developing KPIs, establishing Quality meetings and participating in governance forums

  • Support inspection preparation and management, prior to, during and following any Authority inspection; Support manufacturing locations as required.

  • Support the GDP Management Review process; Review and assess the risk of inputs such as metrics, regulatory intelligence, and identified risks and gaps; recommend mitigation approaches.

  • Participate in New Product Launch activities to ensure that Quality related actions are planned into projects and completed in line with the commitments, e.g., QMS build out, audits, and Quality Agreements.

  • Act as QA assessor/approver on Change Controls: resolve gaps, approve change plans, classifications, strategy for GDP/GMP actions.

  • Develop, utilize and continue to mature tools to ensure efficiency in execution of Distribution Quality Processes

Qualifications/Requirements/Skills:

  • GDP & GMP work experience, or relevant comparable background.

  • Expert knowledge of International GDP regulations; broad knowledge of GMP and GVP regulations,

  • Knowledge and demonstrated experience in application of risk-based quality principles in a pharmaceutical environment.

  • Demonstrated capability to lead a team through organisational change and a dynamic/ evolving business model.

  • Proven leadership ability to design/evolve and implement quality strategies to support their commercial and supply chain partners in both a clinical and commercial setting.

  • Strong ability to collaborate cross functionally across all levels of the organization with strong communication skills and the ability to persuade others to adopt a new point of view, achieve consensus and negotiate effectively,

  • Highly skilled at managing change, and driving Continuous Process improvements,

  • Highly skilled at time and resource management, prioritization of own work and departmental initiatives, and planning/organization skills,

  • Highly skilled in technical writing,

  • Demonstrates advanced ability to effectively communicate to local, international and global audiences,

  • Significant experience in managing/leading others to include performance management and career development,

  • Strong problem solving and critical thinking skills, accompanied by Analytical thinking/Data Analysis skills required to make sound decisions

  • Demonstrates the Vertex behaviours.

  • Proficiency in using Microsoft Office applications required (MS Word, MS Excel, MS PowerPoint).

Education and Experience:

  • Bachelors degree in a scientific or allied health field

  • Typically requires 10 years of relevant work experience, or the equivalent combination of education and experience

We’re enabling flexibility and choice between individuals and their managers to maintain our strong culture of collaboration and ensure a daily vibrancy within our sites globally. In this Hybrid or On-Site-Eligible role, you can choose to work:

1. Hybrid and work remotely up to two days per week; or select

2. On-Site and work 5 days per week with ad hoc flexibility.  

#LI-AR1  #LI-Hybrid

Pay Range:

$182,300 - $273,500

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]

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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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