Kindeva Drug Delivery

Senior Training Specialist

Kindeva Drug Delivery  •  Missouri (Onsite)  •  1 month ago
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Job Description

Our Work Matters
At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.
The Impact You Will Make
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.

#LI-ON-SITE

California residents should review our Notice for California Employees and Applicants before applying.

Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees—regardless of format—without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.

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.

Do you see yourself as part of the Kindeva mission? Click Apply Now Today!
Kindeva Drug Delivery

About Kindeva Drug Delivery

Kindeva is a purpose-fueled, people-centric CDMO dedicated to advancing your project, your ambitions, and our industry. With a legacy of innovation and deep expertise in complex drug development, we serve as a trusted partner to pharmaceutical companies worldwide.

For us, fast-tracking healthier tomorrows starts with industry-leading finished-dose expertise. From early-stage formulation to full-scale commercial production, we optimize every step to help bring life-changing therapies to patients faster.

Built on a rich heritage of regulatory diligence and blockbuster devices, our expertise sharpens, optimizes, and maximizes your project—combining best-in-class facilities with specialist capabilities in injectable, inhalation, and dermal delivery, to ensure exceptional-by-design solutions throughout.

Strategically minded and dedicated to your lasting legacy, we provide value beyond manufacturing, turning your long-term possibilities into achievable milestones.

Because every patient deserves tomorrow.

For more information about how we can transform tomorrows together, please visit www.kindevadd.com.

Industry
Chemicals & Materials
Company Size
1,001-5,000 employees
Headquarters
Woodbury, Minnesota
Year Founded
2020
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