GMP onboarding raises questions that ordinary onboarding doesn't. Are contractors treated like long-term employees? Where does GMP training end and HR training begin? When can new people start working, and how should new hires differ from internal transfers?
This 90-minute webinar answers those onboarding FAQs and shows how a well-designed program becomes part of your company culture, improving new hire retention and getting people contributing independently sooner. You'll cover management's expectations, HR onboarding, quality's role, GMP training requirements, full-time staff versus contractors and temporary personnel, and benchmarks for training and competency.
WHY SHOULD YOU ATTEND?
Onboarding is your one chance at a first impression and shapes early motivation, while compliance, quality culture and work culture all need attention. Many hiring managers struggle with it, yet a few simple steps can produce a successful, compliant program.
The session suits training managers and professionals, instructional designers, HR staff who coordinate with GMP training, QA/QC, manufacturing and operations supervisors, auditors, compliance officers, validation staff, technical writers and counsel.
AREA COVERED
- FAQs for employee onboarding
- Management's expectations for new employees
- HR onboarding
- Quality's role in onboarding
- GMP training requirements
- Full-time employees vs contractors and other temporary personnel
- New employees vs internal transfers
- Benchmarks for training and competency
LEARNING OBJECTIVES
- Define the onboarding process in the context of compliance
- Work with Human Resources on a coordinated onboarding strategy
- Differentiate training requirements for full-time employees and contractors
- Distinguish training needs for new hires and internal transfers
- Prioritize training items to ensure compliance
- Shorten the learning curve for new or transferred employees
WHO WILL BENEFIT?
This course will be of benefit to anyone responsible for managing or delivering training in a GMP environment, and HR employees who interact frequently with the GMP training organization to coordinate onboarding.
- Training department management
- Human Resource personnel
- Training professionals
- Instructional designers
- Supervisory management of operational departments
- QA/QC personnel
- Manufacturing managers/supervisors
- Pharmaceutical and cGMP auditors
- Compliance officers
- Validation specialists, scientists, engineers
- Medical/technical writers
- Consultants/service providers
- Engineering and design controls teams
- General/corporate counsel
Onboarding is your one chance at a first impression and shapes early motivation, while compliance, quality culture and work culture all need attention. Many hiring managers struggle with it, yet a few simple steps can produce a successful, compliant program.
The session suits training managers and professionals, instructional designers, HR staff who coordinate with GMP training, QA/QC, manufacturing and operations supervisors, auditors, compliance officers, validation staff, technical writers and counsel.
- FAQs for employee onboarding
- Management's expectations for new employees
- HR onboarding
- Quality's role in onboarding
- GMP training requirements
- Full-time employees vs contractors and other temporary personnel
- New employees vs internal transfers
- Benchmarks for training and competency
- Define the onboarding process in the context of compliance
- Work with Human Resources on a coordinated onboarding strategy
- Differentiate training requirements for full-time employees and contractors
- Distinguish training needs for new hires and internal transfers
- Prioritize training items to ensure compliance
- Shorten the learning curve for new or transferred employees
This course will be of benefit to anyone responsible for managing or delivering training in a GMP environment, and HR employees who interact frequently with the GMP training organization to coordinate onboarding.
- Training department management
- Human Resource personnel
- Training professionals
- Instructional designers
- Supervisory management of operational departments
- QA/QC personnel
- Manufacturing managers/supervisors
- Pharmaceutical and cGMP auditors
- Compliance officers
- Validation specialists, scientists, engineers
- Medical/technical writers
- Consultants/service providers
- Engineering and design controls teams
- General/corporate counsel
Speaker Profile
Michael Esposito
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 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 Johnson & Johnson Consumer Healthcare and revised their introductory GMP course. He is a member of the training organizations GMP Training Educators Association and Association for GXP Excellence and …
Upcoming Webinars
NEW Nacha Rule - Third-Party Sender (TPS) Roles and Respons…
Paying and Receiving Payments for Referrals: You Can Go to …
FDA Technology Modernization Action Plan (TMAP) and Impact …
Human Factors Usability Studies Following ISO 62366 and FDA…
Validation Statistics for Non-Statisticians
Construction Lending And Real Credit Administration: Evalua…
Thriving in a Hybrid Workplace: Keys to Leadership and Team…
Excel Power Skills: Master Functions, Formulas, and Macros …
Discover how Emotional Intelligence turns AI from a technic…
Batch Record Review and Product Release
Tattoos, hijabs, piercings, and pink hair: The challenges …
Handbook Overhaul 2026: Compliance, OBBB Act & Beyond
Copilot and HR: An Introduction for HR Professionals
Female to Female Hostility @Workplace: All you Need to Know
ChatGPT for HR - Build HR Policy Framework and Strategy
Excel Spreadsheets; Develop and Validate for 21 CFR Part 11…
Major cGMP Issues: FDA Concerns in 2026
The Perfect Storm Coming to Healthcare: Value Based Care Me…
Fostering a Culture of Respect: Eliminating Gossip, Rumour…
Language is Code - Intro to AI - Generative AI - ChatGPT an…
Excel + AI: The Smart User's Guide to Faster, Easier Work w…
The Importance of the first 5 seconds when presenting
Managing Difficult Employee Conversations
ChatGPT and Project Management: Leveraging AI for Project M…
I-9 Audits: Strengthening Your Immigration Compliance Strat…
Pivot tables beginner to advanced + 20 advanced Pivot table…
Emotional Intelligence: Mastering the Emotions of Great Lea…
2026 Nacha Rules Changes (Part 1): Fraud Monitoring & Ops B…
Accounting For Non Accountants : Debit, Credits And Financi…
Medical Device Cybersecurity Following FDA’s 2026 Premarket…
Performance of Root Cause Analysis, CAPA, and Effectiveness…
Human Error Reduction Techniques for Floor Supervisors