Skip to main content

Associate Director, R&D Quality Learning Development Lead

Lexington, Massachusetts

Lexington, Massachusetts| Zurich, Switzerland

Apply Now

At Takeda, Quality has always been a priority for us, throughout our long history. Today, what we do in Global Quality touches every part of our diverse organization. It’s reflected in our end-to-end Quality Management System that encompasses R&D, Manufacturing & Distribution, Commercial, Vaccines and our BioLife Plasma collection network. When you’re a part of our team, you’ll do meaningful work that makes an impact on the lives of patients. Learn more about us and explore the opportunities to build a remarkable career.

Job ID R0136739 Date posted 10/18/2024 Location Lexington, Massachusetts

Lexington, Massachusetts| Zurich, Switzerland

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’sPrivacy Noticeand 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

Job Title: Associate Director, R&D Quality Learning Development Lead

Location: Lexington, MA

About the role:

As the Associate Director, R&D Quality Learning Development Lead you will identify learning journeys and curricula, and the creation of learning content within the R&D and R&D Quality organization. You will lead training needs analysis using a risk-based model to determine the relevant training required to support the relevant functions in partnership with the relevant R&D functional leaders, R&D Quality (RDQ) functional leaders, business process owners and key learners. You will be responsible for content development, learning experience and instructional design, and creation of tools and templates to support the development and revision of learning deliverables.

How you will contribute:

  • Assess performance and monitor progress on deliverables assigned to them, ensuring learning content completion and approvals are achieved.
  • Implement and maintain procedural learning development and curricula design standards (following Global Standards and SOPs), guidance and support for identification of necessary modalities to support earning development, and learning partnership with key R&D and RDQ stakeholders.
  • Drive continual improvement for learning content deliverables for relevant functions within R&D and R&D Quality, leveraging best-in-class industry standards, innovative approaches, and new technologies, through partnerships with the functions.
  • Lead key process improvement and learning projects within R&D and R&D Quality, partnering with internal and external stakeholders to identify process and/or learning gaps; establish milestones and deliverables to address the gap(s) identified
  • Lead the design, development, and implementation of relevant R&D learning programs, including assessment of translation requirements, learning management system (LMS) curricula design, learning experience design, assignment strategy, and end-user support
  • Lead efforts (using Kaizen, Six Sigma, Gemba Walk, Empathy maps), to identify and improve end-user performance and learning effectiveness in partnership with the R&D business.
  • Ensure R&D learning programs are designed, developed, and distributed effectively, and meet all applicable regulatory requirements, in close coordination with R&D functions.
  • Ensure all deliverables are tracked and delivered on time, and learning KPIs are identified and monitored for determination of training effectiveness and retention, in close coordination with R&D functions.
  • Provide learning design support within appropriate systems: Ensuring all learning content is uploaded in the Document Management System (DMS), all content (for mandatory training) is compiled into appropriate curricula in the Learning Management System (LMS) and additional supplementary content is created or curated within the Learning Experience Platform (LXP).
  • Provide process and system training on activities related to the R&D QCS documentation and learning programs
  • Lead workshops to drive a culture of Documentation and Learning Excellence across the R&D organization
  • Provide harmonized learning design, ensuring high-quality content, format and metadata for learning content stored within the DMS.
  • Be a qualified Master Trainer to train and qualify trainers across the R&D and R&D Quality organization who will deliver Instructor-led training (ILT) or On-the-job training (OJT) GxP training.
  • Provide guidance on learning best practices for stakeholders, following the training need analysis and risk-based approach defined to develop learning content within the R&D and RDQ organization.
  • Uploads supportive documentation for learning deliverables into the DMS (e.g., storyboards, overview presentations, SCORM packages) for internal and external audits and regulatory inspections.

What you bring to Takeda:

  • BS/BA degree required.
  • Minimum 8 years' experience in Learning, Training, and/or Process Excellence/Continuous Improvement in a regulated industry
  • Experience as project/people manager; leading large-scale, cross-functional, global projects with multiple stakeholders
  • Experience designing and developing eLearning solutions (Vyond, Smartsheet, Captivate, Storyline…) would be ideal
  • Fluency in written and spoken English
  • Experience facilitating large workshops and/or training classes
  • Experience with Change Management
  • Proficient in managing multiple projects simultaneously
  • Strong computer skills, including Microsoft Office suite and experience with other innovative collaboration tools and technology

Important Considerations:

At Takeda, our patients rely on us to deliver quality products. As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product. In this role, you may:

  • May be required to wear personal protective equipment (PPE) and other clean room garments daily. This may include safety shoes, safety glasses, aprons, face shields, lab coats, full body gowns, hair nets and gloves and hearing protection.
  • Need to remove all make-up, jewelry, contact lenses, nail polish and/or artificial fingernails while in the manufacturing environment.
  • Work in a cold, wet environment.
  • Work multiple shifts, including weekends, or be asked to work supplemental hours, as necessary.
  • Work around chemicals such as alcohol, acids, buffers and Celite that may require respiratory protection.

More about us:

At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.

Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

#GMSGQ #ZR1 #LI-MA1

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:

149,100.00 - 234,300.00

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-termincentives. 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, MAZurich, Switzerland

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

Job Exempt

Yes
Apply Now

Working at Takeda

  • Inclusion

    Here, you will feel welcomed, respected, and valued as a vital contributor to our global team.
  • Collaboration

    A strong, borderless team, we strive together towards our priorities and inspiring mission.
  • Innovation

    Bold initiatives, continuous improvement, and creativity are at the heart of how we bring scientific breakthroughs from the lab to patients.
  • Top Workplace

    Recognized for our culture and way of working, we’re one of only 17 companies to receive Top Global Employer® status for 2024.
  • Work-Life

    Our people-first mission extends beyond patients to include their families, communities, and our own Takeda family.
  • Empowerment

    Through trust and respect, you will have genuine support from leaders, managers, and colleagues to do your best work.

What we believe in

Our values of Takeda-ism are Integrity, Fairness, Honesty and Perseverance, with Integrity as the core. These are brought to life through actions based on Patient, Trust, Reputation and Business, in that order.

Our belief in putting people first extends beyond our patients — it includes their families and communities, as well as our Takeda colleagues and their families.

We are committed to embracing our differences, valuing different perspectives, and fostering a culture of respect, inclusiveness and empowerment.

Our embedded Diversity, Equity & Inclusion (DE&I) strategy enables us to attract and retain exceptional talent, drives innovation, and helps address systemic inequalities in our communities.

  • Integrity

  • Fairness

  • Honesty

  • Perseverance

We're Steadfast In Our Commitment to Four Key Imperatives

Patient


Responsibly translate science into highly innovative medicines and accelerate access to improve lives worldwide.

People


Create an exceptional people experience.

Planet


Protect our planet.

Data & Digital


Transform Takeda into the most trusted, data-driven, outcomes-based biopharmaceutical company.

Join our talent community

Get customized job alerts sent right to your inbox. Plus, get the latest in company news and other important resources by signing up for our talent community.

Learn about job updates