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Recorded WebinarNew

Onboarding In A GMP Environment — Best Practices

Build a compliant and effective GMP onboarding program — cover training coordination, contractor vs. employee differences, and how to reduce the compliance learning curve.

4.8(0 reviews)
1.5 hours
Michael Esposito

Instructor

Michael Esposito

GMP Training & Document Management Specialist

What You'll Learn

How to define the onboarding process in the context of GMP compliance
Where GMP training ends and HR training begins
How to differentiate training for new employees vs. internal transfers
Training requirements for full-time employees vs. contractors
How to coordinate with HR to create an integrated onboarding strategy
How to prioritize training items to ensure compliance and reduce the learning curve

About This Event

Onboarding in a pharmaceutical GMP environment is a difficult task. Compliance considerations, quality culture, and work culture are all important points of focus. This interactive 90-minute course addresses the issues that accompany onboarding new or transferred employees and enables you to customize your efforts based on job function. Topics include where GMP training ends and HR begins, when employees can begin working, and how to differentiate training for new vs. transferred employees. Participants will learn to interact with Human Resources to create a coordinated onboarding strategy and prioritize training items to ensure compliance. Code: FDB2885

Curriculum

Defining the Onboarding Process in the Context of Compliance
12 min
GMP Training vs. HR Training — Where the Lines Are Drawn
12 min
New Employees vs. Internal Transfers — Different Requirements
12 min

Requirements

  • Hiring managers, supervisors, and HR employees in GMP manufacturing environments
  • Applicable to training managers and anyone responsible for onboarding manufacturing personnel in life sciences

Meet Your Instructor

Michael Esposito

Michael Esposito

GMP Training & Document Management Specialist

Michael Esposito has 30 years experience in the pharmaceutical industry and 13 years experience in GMP training and document management. He has worked for Wyeth Pharmaceuticals, Pfizer and Johnson & Johnson's McNeil Consumer Healthcare Division in areas including Packaging, Quality Assurance, Government Contracts, translations, systems training, and international operations. He collaborated in the development and implementation of the training portion of the Consent Decree workplan for McNeil and revised their introductory GMP course. He is a member of the training organization GMP TEA and is fully fluent in Spanish.

30 Years Pharmaceutical IndustryPfizer & J&J AlumniGMP TEA MemberConsent Decree Expert
Quantity
1

Recording – 1 Viewer

$450.00
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Certificate of completion

Event Details

Format

Recorded Webinar

Duration

1.5 hours

Certificate

Included

Access

Lifetime

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