GMP Operational Quality Senior Manager

Job Description

General/Position Summary

SeniorManager, GMP Quality Operationsis a technical resource in the principles and application of quality assurance and compliance. TheSr.Manager coordinates or executes activities on a wide range of projects and takes a role in the design and execution of new projects.Theroleisresponsible formaintainingdocuments reconciliation, labeling control, master batchrecordsand issuance of batch records for production.The quality senior manageris responsible forimplementing strict issuance tracking, controlling version updates, and ensuring data integrity (ALCOA+) to prevent unauthorized changes and ensure product safety

The role will closely partner with operational stakeholders to lead product disposition activities and resolution. A key expectation is the ability to closely collaborate and build relationships with internal and external stakeholders for advancing quality outcomes and operational excellence.

Key Duties & Responsibilities

• AuthorSOP'sto support commercial quality functions.

• Assistwith regulatory agency inspections

• Ensuring that Master Batch Records are managed to maintain compliance over the life cycle.

• Identifyandfacilitatecontinuous improvement efforts

• Managing the issuance of BPRs, ensuring onlyauthorized,current versions are printed for production.

• Maintaining logs for the issuance, return, and reconciliation of batch records to prevent misuse and ensure accountability.

• Ensure audit readiness:Maintainingorganized, accessible documentation for regulatory inspections

• Establishment of quality oversight for internal quality and external CDMO operations for the batch disposition process, across development, launch and commercial manufacturing.
• Manage the day-to-day timely release of finished product to ensure compliance with Regulatory and Vertex cGMP requirements.
• Assure disposition activities across CGT Therapy related products manufacturing are compliant and consistent.
• Develop, establish, and implement Batch disposition operational Quality and Compliance metrics.
• Act as the batch disposition subject matter expert (SME) in support of regulatory inspections and audits, respond to information requests, adjudicate compliance discussions, and negotiate any required corrective actions.
• Identify and communicate risks and assist with risk mitigation plans as necessary.
• Represent Quality to lead/participate in complex projects and partner with key stakeholders for alignment in strategic and operational planning.
• Participate and lead GxP Cell & Gene Therapy Management Reviews to gain insights regarding efficiency and operational performance across the GXP operations, including identification of opportunities for improvement and associated actions.
• Lead and mentor other team members, support development of organizational capabilities and talent building.
• Manage the department resources with regards to budget and personnel.
• Build strategic relationships with internal and external partners - CDMOs within the Quality organization to ensure Quality issues are raised and addressed, as necessary.

Required Education Level

• Bachelor's degree or Masters degree relevant comparable background.

Required Experience

8+ years of experience and 5+ years in a management/supervisory role, or the equivalent combination of education and experience in a regulated pharmaceutical environment

Required Knowledge/Skills

• In-depth global health regulatory agency knowledge and experience across GXP life cycle in Cell & Gene therapy and/or Biologics (EU GMPs, FDA 21CFR Part 1271, GxPs).
• Broad and current knowledge of batch disposition industry trends and best practices in Cell/Gene therapies.
• Preferred QA Operational experience for Autologous Cell Therapy Operations.
• Broad technical knowledge in Cell technology, aseptic manufacturing technology, analytical assays, cell & genetic therapies/Biologics processing, fill/finish and testing.
• Demonstrated strategic planning and execution skills required for operational effectiveness and compliance. Proven ability with Root Cause Analysis, data analytics, and other Operational Excellence experience, such as LEAN, DMAIC, Six Sigma.
• Excellent communication skills and a proven track record Influencing/building/promoting a culture of Quality and Excellence.
• Ability to apply risk management principles to decision making and operational priorities.
• Critical Thinking and Problem Solving skills
• Ability to closely collaborate and build relationships with internal and external stakeholders.

Other Requirements
Up to 15% Travel may be required

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Pay Range:

Disclosure Statement:

Flex Designation:

Flex Eligibility Status:

In this On-Site designated role, you will 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.

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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