Senior Training Specialist

At Kindeva, we make products that save lives, ensuring better health and well‑being for patients around the world. We're driven by our mission to serve as a world‑class, global CDMO that enables the next generation of medicines through excellence in drug delivery. Guided by our vision of Manufacturing More Tomorrows™, our KIND values define how we work and how we deliver what matters. The Senior Training Specialist is responsible for designing, delivering, and maintaining robust training programs that ensure personnel within the CDMO facility are fully qualified to perform their roles in compliance with regulatory, quality, and safety standards. This role supports cross‑functional teams—including Manufacturing, Quality, QC, Engineering, Supply Chain, and MSAT—by coordinating onboarding, technical skills development, and ongoing training initiatives aligned with cGMP requirements. The successful candidate will collaborate with subject matter experts to develop learning solutions; develop and maintain training tools (curricula, OJTs, SOPs, e‑learning); deliver training; assure site compliance with Quality Standards; roll‑out site training initiatives; and achieve compliance and business results through strong partnerships with other site functions. Responsibilities Develop, implement, and continuously improve training curricula for manufacturing operations, quality systems, and other GxP‑regulated functions. Deliver instructor‑led training (ILC) sessions, hands‑on training, and blended learning modules. Collaborate with subject matter experts (SMEs) to create clear, accurate SOP‑based training materials. Ensure training aligns with EU Annex 1, FDA, EMA, ICH, and other applicable regulatory expectations. Ensure training content and execution meet internal and external audit expectations. Support regulatory inspections by providing training documentation and acting as the training SME. Identify gaps in training programs and lead corrective and preventive action (CAPA) activities. Manage onboarding programs for new hires in GxP and non‑GxP functions. Coordinate cross‑training initiatives to support operational flexibility. Facilitate competency assessments and qualification programs for critical job tasks. Analyze training effectiveness using feedback, performance data, and error/trend reports. Recommend and implement improvements to training delivery, materials, and workflows. Champion adult learning principles and modern training methodologies within the organization. Qualifications Bachelor’s degree in Life Sciences, Education, Organizational Development, or related field (or equivalent experience). 3+ years of experience in a pharmaceutical, biotech, or CDMO environment preferred. Must have experience working in a highly regulated manufacturing environment. Knowledge of cGMP, GxP, and regulatory expectations for training and documentation. Experience with electronic Learning Management Systems (LMS/TMS). Strong communication, facilitation, and interpersonal skills. Ability to collaborate with SMEs across technical functions. Experience designing technical training for aseptic processing, biologics manufacturing, packaging and inspection, or sterile fill–finish operations preferred. Certification in training, instructional design, or adult learning (e.g., ATD, CPTM) preferred. Demonstrated experience supporting regulatory inspections. Familiarity with risk‑based training approaches and quality systems. Strong working knowledge of Adult Learning Principles. Equal Opportunity Employer Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law. Job Family C - Training & Development - Training Delivery #J-18808-Ljbffr