Associate Director, QMS Training & Document Management (Global R&D & PV QA)

At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. Job Summary The Associate Director, QMS Training Management (Global

R D & PV QA

) reports to the Head Global Quality Management System (QMS) (Americas/Europe) and is responsible for managing and supporting the implementation of the global

GCP/GVP/GLP

training and onboarding strategy, training development and delivery, and measuring training effectiveness and compliance. The Associate Director will play a global training lead role in supporting the global R D, PV, MA, and QA organizations to ensure the

GCP/GVP/GLP

training and communication strategies, processes, procedures, programs, and systems comply with applicable

GCP/GVP/GLP

standards, relevant regulatory requirements, and applicable Daiichi Sankyo policies and procedures.

Job Description Training Program Management:

Manage the creation and implementation of training courses as identified in annual training plans, role-based training curricula, GCP/GVP/GLP computer systems training plans, and other projects as needed in collaboration with functional leaders, SMEs/SOP authors, training vendors, and regional/local training leads. Assess training needs and determine optimal training delivery approach, training audience, and communication strategy in a training implementation plan with global/local training leads, SMEs/SOP Authors Facilitate identifying training content for development and delivery with functional leaders and SMEs/SOP Authors. Oversee/manage the creation of training courses in various modalities, including blended approaches (e.g., instructor-led training, eLearning, etc.) with SMEs/SOP Authors, vendors. Engage with and manage external training vendors as required to ensure training content availability and delivery. Create, implement, and maintain the global

GCP/GVP/GLP

New Employee Onboarding program that ensures effective functional onboarding of

GCP/GVP/GLP

resources by partnering with functional leaders and representatives. Oversee/manage the global and local learning management system activities, including role-based training curricula development and administration, training and roster registration/assignment, course creation and availability, and training histories. Qualify

GCP/GVP/GLP

SMEs identified to deliver instructional design/adult learning principles training by implementing the SME Train-the-Trainer qualification program. Stay current with industry-leading training practices and incorporate them into

GCP/GVP/GLP

training. Partner with Global QA leaders, functional leaders, or their SMEs to incorporate CAPAs and lessons learned into training activities. Qualifications Education A Bachelor's Degree in a science-related discipline required. A higher-level degree such as a Master's Degree is preferred Basic Requirements 7 or more years of professional pharmaceutical industry experience managing GxP learning development activities in the pharmaceutical or biotech industry, or equivalent experience is required. Must have in-depth knowledge of Quality Management Systems and related GxP principles: Broad understanding of global expectations of Regulatory Health Authorities Extensive knowledge with managing global Training Programs, Development, Implementation, Management, including System management application Strong interpersonal and prioritization skills with demonstrated ability to build collaborative relationships Excellent problem solving and decision-making skills. Skilled at conflict resolution / negotiation. Organization awareness (e.g., interrelationship of depts., business priorities), including significant experience working cross-functionally and in global teams across different regions of the world Experience with participation in regulatory inspections presenting or defending subject matter area in audits or regulatory inspections. Understanding and familiarity with FDA, EMA, MHRA, and other European and international regulatory requirements, guidelines Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.

Salary Range:

USD$150,800.00 - USD$226,200.00 Download Our Benefits Summary PDF