Sr. Manager, R&D Quality Compliance and Systems

Company: Takeda
Location: Lexington
Posted on: April 1, 2026

Job Description:

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description Title: Sr. Manager, R&D Quality Compliance and Systems Location: Lexington, MA About the Role: As a Sr. Manager, R&D Quality Compliance and Systems, you will provide cross functional expertise and input to the quality systems supporting Takeda’s R&D Quality organization across the RDQ enterprise and ensuring that it is robust, aligned with, and compliant to applicable regulatory requirements, and governed and positioned for continual improvement. You will provide key input to the establishment of the framework for quality oversight of the R&D Quality Management System. Serve as a Quality Partner across R&D Quality and contribute to the design, implementation and advancement of the R&D Quality Management System operations. How will you contribute: Responsible for autonomously executing activities associated with the RDQ framework of audit and inspection management, inspection readiness, gap assessments, risk management and incident escalation. Partners with RDQ to develop plans for R&D audit programs and inspection preparation to minimize critical observations and ensure Takeda’s regulatory reputation remains positive with global authorities. Responsible for the implementation of Risk Management principles across RDQ, ensuring consistency of approach and compliance to SOPs. Responsible for authoring, editing, and circulating for approval the associated family of documents. Ensure the execution of the RDQ Regulatory Intelligence program, reviewing, documenting and gap assessing global regulatory changes across all GxPs (GMP, GCP, GDP, GLP, PV) used within R&D/R&D Quality to ensure continued compliance with current global regulations. Accountable for application of the gap assessment process, ensuring consistency of approach and compliance to SOPs. Responsible for identifying and executing on process improvements that are identified associated with the process. Steward the R&D Quality Management System, ensuring R&D and R&D Quality remain in compliance with Global GxP regulations in coordination with the R&D Quality Compliance team. Serve as system owner for centrally accessed QMS processes Advances R&D/RDQ-wide forums to increase awareness, foster cross-functional learning, and improve knowledge. Develops metrics, trending programs, and continuous improvement plans for processes and systems used across R&D/R&D Quality. Lead and independently execute projects which enhance RDQ’s efficiencies and innovation. Engages in global, enterprise-wide cross-functional projects and programs on behalf of RDQ. Provide subject matter expertise and consultation for R&D Compliance related to deviations, CAPAs, change controls, responses to inspection outcomes and incident escalations. Working knowledge of current GxP (e.g. Good Manufacturing Practice, Good Laboratory Practices, Good Clinical Practices, Pharmacovigilance) requirements for the pharmaceutical industry. Experience in compliance and systems related processes and tasks. Experience with risk management strategies and general project management. Proven success in identifying and implementing continuous improvement initiatives. Proficient in analyzing data to identify performance trends. Ability to proactively manage the development and re-engineering of key processes and systems in support of the business’s mission. Able to manage projects, programs and tasks with little, to no, oversight. Able to analyze data and make recommendations to management and/or escalate as appropriate. Experience working within complex/matrixed organizations. Ability to read, analyze and interpret common scientific and technical data/reports and legal/regulatory documents. Effectively presents information to management, internal groups, and stakeholders. Ability to anticipate potential problems and risks related to quality expectations and regulatory compliance, formulate action plans, and implement solutions. Ability to work effectively in a fast paced, rapidly changing environment and to work on multiple work streams and projects simultaneously. What you bring to Takeda: Bachelor’s Degree in Chemistry, Biology, Engineering, or related field. Minimum of 8 years professional working experience in the field of healthcare products or related activities such as pharmaceutical or device manufacturing, Quality Control or Quality Assurance including at least 4 years in GMP Quality or Compliance. Six sigma/lean processing, project management professional and/or auditor certification preferred. Takeda Compensation and Benefits Summary We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. For Location: Lexington, MA U.S. Base Salary Range: $137,000.00 - $215,270.00 The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location. U.S. based employees may be eligible for short-term and/ or long-term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation. EEO Statement Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law. Locations Lexington, MA Worker Type Employee Worker Sub-Type Regular Time Type Full time Job Exempt Yes It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Keywords: Takeda, Manchester , Sr. Manager, R&D Quality Compliance and Systems, Science, Research & Development , Lexington, New Hampshire