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Catalent Inc

Instructional Designer

Catalent Inc, Kansas City, Missouri, United States, 64101

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Instructional Designer

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. Catalent's Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. The site provides a range of integrated services for oral solid dosage forms, from formulation development and analytical testing to clinical and commercial-scale manufacture. The Kansas City facility is a Center-of-Excellence for our Biologics Analytical Services business. Our talented team has over 25 years of experience providing analytical services for stand-alone and integrated biologics projects. Catalent Pharma Solutions in Kansas City, MO is hiring an Instructional Designer. The Instructional Designer position is responsible for developing and implementing highly professional, effective, engaging, and innovative training/educational content for sitewide application as well as customized content for individual business units, departments, and teams. The Instructional Designer will work in cooperation and alignment with site leadership and departmental training personnel across the site to design, plan, implement, maintain, and grow our GMP training program. This is a full-time, salary, onsite position. This is a 1st shift position. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee. The Role

Develop, implement, and manage high-quality training content for both GMP and non-GMP purposes, following principles of instructional design. Assist Manager, Training Systems, with measurement and evaluation of the effectiveness of the overall site training program by conducting routine system assessments and providing input to development of long-term plans to enhance overall effectiveness of the training program. Support Operations training personnel in providing role-specific training to site personnel by offering guidance on best practices for delivering training to adult learners. Perform hands-on and instructor-led classroom training, focusing on individual target groups. Partner with OJT trainers and department personnel to develop training modules and programs. Serve as internal consultant to management, focused on targeting performance improvement needs, providing feedback, and recommending training and non-training solutions, including human reliability and investigations of human errors. Create and manage metrics and KPIs to measure the effectiveness of site training processes & systems, including pre- and post-assessments, surveys, and feedback loops to ensure continuous improvement. Clear understanding of SOPs, cGMP, and applicable pharmaceutical regulations as required to accomplish daily tasks and projects, including Learning Management System administration. All other duties as assigned. The Candidate

Bachelor's degree in education, instructional design, or related field required. 3+ years of responsibility for content development/instructional design or other relevant experience. 2+ years of experience delivering educational content to adult learners. Expertise in the use of Learning Management Systems (LMS), AI, content authoring tools (i.e., Articulate, Camtasia, etc.), and/or multimedia editing software required. Knowledge of GMP and compliance training, with the ability to develop content that meets strict industry standards highly desired. Why You Should Join Catalent:

Defined career path and annual performance review and feedback process Diverse, inclusive culture Positive working environment focusing on continually improving processes to remain innovative Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives 152 hours of PTO + 8 paid holidays Several Employee Resource Groups focusing on D&I Dynamic, fast-paced work environment Community engagement and green initiatives Generous 401K match Medical, dental and vision benefits effective day one of employment Tuition Reimbursement - Let us help you finish your degree or start a new degree! WellHub- program to promote overall physical wellness Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. Personal initiative. Dynamic pace. Meaningful work.