Onboarding Employees in a GMP Environment: Best Practices for Foundational Employee Success
This course will address the issues that accompany onboarding new or transferred employees and enable you to navigate them successfully, Learn to interact with Human Resources to create a coordinated onboarding strategy, A successful onboarding strategy will combine the inputs of all these stakeholders and help create a consistent and well-understood process for the company.
Monday, June 28, 2021
10:00 AM PDT | 01:00 PM EDT
More Trainings by this Expert
Product Id : 503832
Live: One Dial-in One Attendee
Corporate Live: Any number of participants
Recorded: Access recorded version, only for one participant unlimited viewing for 6 months ( Access information will be emailed 24 hours after the completion of live webinar)
Corporate Recorded: Access recorded version, Any number of participants unlimited viewing for 6 months ( Access information will be emailed 24 hours after the completion of live webinar)
The FDA's expectations for training new employees are summed up in 21 CFR 211.25(a), i.e., pharmaceutical professionals require the education, training and experience to complete their job functions.
Onboarding new or transferred employees in a Pharmaceutical Good Manufacturing Practices (GMP) environment and ensuring compliance with these requirements create some unique challenges.
Although FDA expectations provide some of the framework regarding types and frequency of training, there are decisions that the company will need to make in light of its evaluation of how to best achieve compliance for its employees, maintain a quality culture, and manage the work environment.
Often there are questions regarding how to translate these requirements to the day-to-day operations of the company. Of particular interest are the different perspectives of onboarding from Human Resources and Quality Assurance (particularly Training), each of which have their own priorities.
Managers, likewise, are eager to have their employees qualified to perform their job functions as efficiently as possible because of pressure to keep pace with the business, and will communicate their expectations to these two organizations.
A successful onboarding strategy will combine the inputs of all these stakeholders and help create a consistent and well-understood process for the company.
Why you should Attend:
Onboarding in a GMP environment leads to some questions and confusion. Are contractors treated the same as long-term employees? Where does GMP Training end and HR training begin? When can employees begin working? How differently should new and transferred employees be treated in the onboarding process?
This course will address the issues that accompany onboarding new or transferred employees and enable you to navigate them successfully.
By the end of this webinar, you should be able to:
- Define the onboarding process in the context of compliance
- Learn to interact with Human Resources to create a coordinated onboarding strategy
Differentiate the training requirements for full-time employees and contractors, and for new employees vs. employees transferring internally
Prioritize training items to both ensure compliance and reduce the learning curve for new or transferred employees.
Areas Covered in the Session:
Who Will Benefit:
- FAQs for employee onboarding
- Management's expectations for new employees
- HR onboarding
- Quality's role in the onboarding process
- GMP training requirements
- Handling full-time employees vs. contractors and other temporary personnel
- Benchmarks for training and competency
In a Pharmaceutical Environment Either at Corporate Offices or At manufacturing facilities or distribution centers:
- Managers with direct Reports
- Human Resources professionals
- Quality Assurance and Training departments
Michael Esposito has over 30 years experience in the pharmaceutical industry and 17 years experience in GMP training and document management. He has worked for Wyeth Pharmaceuticals, Pfizer and Johnson & Johnson's McNeil Consumer Healthcare Division in a variety of areas including Packaging, project administration, 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 organizations GMP Training Educators Association and Association for GXP Excellence (AGXPE) and is fully fluent in Spanish. His areas of interest include systems training, training effectiveness, post-training user support, process improvement, and sustainable packaging.