Senior Manager, RDQ Learning & Documentation Governance

Reposted 24 Days Ago
Be an Early Applicant
Boston, MA, USA
In-Office
129K-194K Annually
Senior level
Biotech • Pharmaceutical
The Role
Lead RDQ learning and documentation governance: establish curriculum governance across GxP domains, partner with Global Quality Training and Documentation, assess and optimize curricula and SOP/work instruction practices, coordinate reviews and effectiveness assessments, drive harmonization, change management, and inspection readiness across cross-functional stakeholders.
Summary Generated by Built In

Job Description

General position summary: 

The Senior Manager, RDQ Learning & Documentation Governance will lead the oversight and coordination of R&D Quality (RDQ) learning governance, documentation governance, and operational readiness activities in partnership across RDQ, with Global Quality Training, Global Documentation, and cross-functional stakeholders.
This role will serve as a central coordinator and governance lead for RDQ learning, documentation, and curriculum management activities, ensuring alignment to evolving regulatory expectations, quality systems, inspection readiness priorities, and organizational transformation initiatives. The individual will drive consistency, oversight, and continuous improvement of the RDQ curricula, such as establishing role based training and partner with stakeholders to develop and enhance role-based learning strategies that support capability development, operational effectiveness, and inspection readiness. In addition, this role will support harmonization and continuous improvement of RDQ documentation and operational practices to strengthen organizational readiness, operational consistency, and quality culture maturity.
Key Responsibilities:

Learning Governance & Curriculum Oversight

  • Establish and maintain governance processes for RDQ curricula across GxP domains (e.g., GCP, GVP, GLP)
  • Partner with Global Quality Training to ensure effective management of role-based curricula, learning pathways and associated training assignments
  • Evaluate existing RDQ curricula to identify gaps, redundancies, inconsistencies, and opportunities for optimization
  • Partner with SMEs and functional stakeholders to enhance curricula based on evolving business processes, regulatory expectations, and organizational priorities
  • Coordinate curriculum review cycles, change management activities, and periodic effectiveness assessments
  • Drive consistency and standardization across RDQ curriculum management practices

Documentation Governance & Operational Alignment

  • Represent RDQ within cross-functional documentation and training governance forums, including the Documentation & Training Process Owner Network (PON)
  • Partner with Global Documentation and RDQ stakeholders to support harmonization and continuous improvement of SOP and Work Instruction governance practices
  • Support development of standardized approaches for procedural documentation and associated training alignment
  • Assess RDQ documentation and training impacts associated with process, governance, or regulatory changes
  • Identify opportunities to streamline and harmonize documentation and training practices across RDQ

Qualifications & Experience:

  • Strong background in Quality Assurance, Compliance, and/or Quality Governance in the pharmaceutical/biotech industry.
  • 5+ years of experience in Quality Systems, GxP operations, compliance, inspection readiness, training governance, documentation management, or organizational capability development
  • Strong understanding of GxP training and documentation requirements and quality system governance
  • Experience working cross-functionally in complex matrix organizations
  • Strong facilitation, stakeholder management, and communication skills
  • Demonstrated ability to drive strategic initiatives, operational improvements, and organizational change

#LI-remote

Pay Range:

$129,400 - $194,200

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:

Remote-Eligible

Flex Eligibility Status:

In this Remote-Eligible role, you can choose to be designated as: 
1.    Remote: work remotely five days per week and come into the office on occasion – you’re always welcome on-site; or select 
2.    Hybrid: work remotely up to two days per week; or select
3.    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-Remote

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

  • Strong background in Quality Assurance, Compliance, and/or Quality Governance in the pharmaceutical/biotech industry
  • 5+ years of experience in Quality Systems, GxP operations, compliance, inspection readiness, training governance, documentation management, or organizational capability development
  • Strong understanding of GxP training and documentation requirements and quality system governance
  • Experience working cross-functionally in complex matrix organizations
  • Strong facilitation, stakeholder management, and communication skills
  • Demonstrated ability to drive strategic initiatives, operational improvements, and organizational change

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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