Training Partner for Global Regulatory Affairs– is that you?
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Ballerup
Do you have a flair for training and adult learning? Do you know the pharmaceutical industry and Regulatory Affairs or would like to learn more about this? Do you want to be part of building a training set-up more or less from scratch and do you want to join a company that has embarked on a very ambitious journey to become the world’s preferred dermatology care partner? Then please continue reading as this may be the job you have been waiting for.
About the job
In Global Regulatory Affairs at LEO Pharma A/S we are looking for a Training Partner who will help us ensure a strong, well-established and well-functioning global organization with skilled and well-trained employees.
You will join a newly established team (Regulatory Projects & Business Support) in Ballerup, Greater Copenhagen, consisting of 10 people working with various tasks either as project managers for strategic business projects, with budgeting, planning and forecasting or with communication.
As Training Partner you will be a key driver in ensuring the right focus and balance to ensure a compliant training setup as a natural part of the daily work in our Global Regulatory Affairs organization.
Your primary tasks will be to:
Implement and drive the global training strategy and training set-up Maintain and develop our global on-boarding program Work with the global Regulatory organization to ensure we have the right training in place Train the trainers in the Regulatory organization ensuring simple and high-quality training exploring possibilities for training in a new way Collaborate with the R&D - and LEO Pharma Academy on how to do training across the organization with special focus on demystifying what Regulatory Affairs is about Look into benchmarking with other companies/ external institutes doing Regulatory pharmaceutical training and explore the possibilities for knowledge sharing and for doing training outside of the LEO organization
In addition to driving the training strategy and set-up you are also expected to do part of the training yourself, as an example basic Regulatory training to both regulatory and non-regulatory employees. Furthermore, you can expect to be involved in regulatory business projects either as project manager or as a project member according to the needs of the organization.
Qualifications
You hold a Master’s degree within Communication, Education or Psychology OR within Life Sciences with a solid training or communication background. Preferably you have experience from Regulatory Affairs or the pharmaceutical Industry.
You know how to utilize your strong social and communication skills to become an excellent go-to person who can lead the way by engaging and motivating colleagues. You have a track record of building strong relations to stakeholders across the organization. You are not afraid to challenge the status quo or look for new ways of doing things aspiring to take training in Global Regulatory Affairs to the next level.
You are fluent in both written and spoken English and you like to work across cultures and skill types in a busy environment. Experience with change management processes and project management will be an advantage but not a prerequisite.
Contact
For more information, please contact Head of Regulatory Projects & Business Support Louise Wanning Tvede Anderson on +45 31587437
About the job
In Global Regulatory Affairs at LEO Pharma A/S we are looking for a Training Partner who will help us ensure a strong, well-established and well-functioning global organization with skilled and well-trained employees.
You will join a newly established team (Regulatory Projects & Business Support) in Ballerup, Greater Copenhagen, consisting of 10 people working with various tasks either as project managers for strategic business projects, with budgeting, planning and forecasting or with communication.
As Training Partner you will be a key driver in ensuring the right focus and balance to ensure a compliant training setup as a natural part of the daily work in our Global Regulatory Affairs organization.
Your primary tasks will be to:
In addition to driving the training strategy and set-up you are also expected to do part of the training yourself, as an example basic Regulatory training to both regulatory and non-regulatory employees. Furthermore, you can expect to be involved in regulatory business projects either as project manager or as a project member according to the needs of the organization.
Qualifications
You hold a Master’s degree within Communication, Education or Psychology OR within Life Sciences with a solid training or communication background. Preferably you have experience from Regulatory Affairs or the pharmaceutical Industry.
You know how to utilize your strong social and communication skills to become an excellent go-to person who can lead the way by engaging and motivating colleagues. You have a track record of building strong relations to stakeholders across the organization. You are not afraid to challenge the status quo or look for new ways of doing things aspiring to take training in Global Regulatory Affairs to the next level.
You are fluent in both written and spoken English and you like to work across cultures and skill types in a busy environment. Experience with change management processes and project management will be an advantage but not a prerequisite.
Contact
For more information, please contact Head of Regulatory Projects & Business Support Louise Wanning Tvede Anderson on +45 31587437
Information og data
Denne ledige stilling har jobtypen "Apoteker", og befinder sig i kategorien "Sundhed og forskning".
Arbejdsstedet er beliggende i Ballerup.
Jobbet er oprettet på vores service den 20.1.2020, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Apoteker
- Ballerup
- Fredag den 31. januar 2020
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