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    Onboarding Employees in a GMP Environment: Best Practices for Foundational Employee Success

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    Website http://bit.ly/2Fi5K4y | Want to Edit it Edit Freely

    Category Online Professional Trainings;world class professionals trainings;professionals training courses

    Deadline: February 05, 2019 | Date: February 06, 2019

    Venue/Country: Online, U.S.A

    Updated: 2019-01-09 17:23:03 (GMT+9)

    Call For Papers - CFP

    Overview

    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 should you 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

    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

    Who Will Benefit

    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


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.