Training Specialist I

Training Specialist I

About Site

Catalents Winchester KY site is the companys flagship U.S. manufacturing location for largescale oral solid dose forms operating from a 180000squarefoot facility with fully integrated development and analytical services. The site specializes in complex and controlledrelease oral dose technologies supporting product development technology transfer and commercial manufacturing across pharmaceutical and consumer health programs. Winchester has a long commercial manufacturing track record having launched 100 products and producing billions of tablets and capsules annually making it a critical site within Catalents oral dose network.

Position Summary

We have an opportunity for a Training Specialist I to join our this role you will coordinate develop implement and maintain site-wide training programs that support employee onboarding GMP compliance operational excellence and workforce development. You will work closely with Production Quality Safety and Human Resources to ensure employees receive effective training and maintain the skills required to perform their roles safely and efficiently. This position also manages training documentation and Learning Management System records while supporting leaders in identifying and addressing training needs across the site.

Shift: Monday-Friday 8 AM - 5 PM
Location: Winchester KY
100% Onsite

The Role

• Lead and facilitate new employee orientation programs

• Coordinate onboarding activities to ensure employees are successfully integrated into the organization

• Deliver introductory GMP safety quality and compliance training

• Partner with hiring managers to ensure timely completion of onboarding requirements

• Support new employee engagement and early development initiatives

• Partner with Production Quality Engineering and Safety teams to identify training needs and develop effective training solutions

• Assist in the development implementation and continuous improvement of training programs for manufacturing employees

• Collaborate with subject matter experts to develop training content for equipment processes standard operating procedures and work instructions

• Monitor employee training progress and communicate completion status to department leaders

• Support initiatives that improve employee capability quality performance right-first-time execution and operational efficiency

• Maintain and administer the sites Learning Management System and training records

• Ensure training curricula assignments and records remain current and compliant with regulatory and business requirements

• Coordinate periodic reviews and updates of training materials and curricula

• Generate compliance reports training metrics and status updates for leadership teams

• Maintain document control for training-related procedures materials and records

• Evaluate training effectiveness through assessments observations and feedback

• Identify opportunities to improve training processes tools and content

• Other duties as assigned

The Candidate

Minimum Requirements

• Bachelors degree in Human Resources Education Organizational Development Life Sciences Business or related field preferred

• High school diploma or GED required

• An equivalent combination of education and relevant experience will be considered

• Strong understanding of GMP quality compliance and manufacturing operations

• Experience managing training records and learning management systems (ComplianceWire)

• Strong presentation and facilitation skills

• Excellent written communication and technical documentation skills

• Ability to develop training materials and instructional content

• Individual may be required to sit and stand for an extended period of time

• Specific vision requirements include reading of written documents and frequent use of computer monitor

Preferred Skills & Background

• Minimum 3 years of experience in a GMP-regulated manufacturing environment preferred

• Experience supporting manufacturing production or operations training is strongly preferred

• Experience delivering training or facilitating group learning sessions preferred

• Experience working within pharmaceutical biotechnology medical device consumer health food or other regulated manufacturing industries

• Experience with adult learning principles and instructional design

• Experience supporting audits and regulatory inspections

• Lean Continuous Improvement or Six Sigma exposure is a plus

Why You Should Join Catalent

• Positive and fast-paced working environment focusing on continually improving processes to remain innovative and dynamic

• Competitive Paid Time Off plus 8 paid holidays

• Medical dental and vision benefits effective day one of employment

• Tuition Reimbursement support to finish your degree or earn a new one

• Site-based Employee Engagement activities such as NCAA Basketball Brackets Golf Scrambles Annual Onsite Pet Adoption Events and Mentorship Partnerships with Local Schools

• Employee Resource Groups focusing on Diversity and Inclusion

• Environmentally friendly community engagement green initiatives including Adopt-a-Highway Clean-up

• Defined career path and annual performance review process with potential for career growth

• WellHub program to promote overall physical and mental 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 7000 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.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability you may submit your request by sending an email and confirming your request for an accommodation and include the job number title and location to . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

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California Job Seekers can find our California Job Applicant Notice HERE.