Regulatory Affairs Advisor
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Søborg
Use your experience to transform Regulatory Affairs
NNIT is looking for a principal advisory consultant with a deep regulatory affairs expertise who wish to make a mark on some of the most exciting IT projects in the Life Sciences industry.
The NNIT Life Sciences Advisory team is at the forefront of advising global pharmaceutical and medical device clients on the latest changes within Regulatory Affairs and the IT impact to the industry. Are you our new colleague?
Your responsibilities as a Regulatory Affairs Advisor
You will join an exciting, international advisory department with highly skilled colleagues that have a deep understanding of the life sciences industry and the ability to bridge this knowledge with digital technologies such as machine learning and Cloud solution such as Veeva Vault.
Working closely with international clients, you will use your experience from Regulatory Affairs to advise and assist companies in a vast array of projects, spanning from RA process optimization to new regulatory changes. You will be expected to advice clients on vendor selections for new IT solutions within the area of electronic document management systems (EDMS), eCTD, labelling and regulatory information management systems (RIMS), including IDMP. You may also have knowledge of Pharmacovigilance or Medical Devices processes and systems.
A key part of the job is business development activities related to new offerings that will support our continued growth within the areas of Regulatory Affairs. The job will include close collaboration with a multitude of stakeholders within NNIT where your specialist knowledge will strengthen our companies' strategic aspirations in Regulatory Affairs. You will also be expected to give presentations and speaker sessions at conferences and write articles about Regulatory Affairs topics.
You will be part of NNIT’s Life Sciences Advisory
NNIT’s Life Sciences Advisory is an ambitious department with a key importance to NNIT’s strategy. We appreciate openness, honesty and a winning attitude.
Our customers expect us to know about upcoming trends and regulatory changes, as well as they expect us to be at the forefront in terms of technical solutions. Your career will include continuous training and competence development to support our department and your personal ambitions.
NNIT was recently nominated as the most attractive workplace within the IT consulting area in Denmark.
Your qualifications and experiences
You hold an MSc degree in Life sciences or IT with 3-5 years of experience from the life sciences industry (preferably Regulatory Affairs). You have a strong understanding of IT, and you manage to bridge your professional experience from the life sciences industry with IT. You must have a curious nature and interest in new technologies.
It is an advantage if you have experience with business processes and regulatory requirements within Regulatory Affairs and that you have a good overall understanding of IT solutions within this area.
You are used to advice and build trust on all levels, and you might have gained this experience from a past job within the consulting area. NNIT has offices in Copenhagen, Frankfurt and Basel, and we will expect you to live in the proximity of these pharma hubs.
Fluency in oral and written English is a must. German or Danish is beneficial. Travel must be expected.
NNIT is looking for a principal advisory consultant with a deep regulatory affairs expertise who wish to make a mark on some of the most exciting IT projects in the Life Sciences industry.
The NNIT Life Sciences Advisory team is at the forefront of advising global pharmaceutical and medical device clients on the latest changes within Regulatory Affairs and the IT impact to the industry. Are you our new colleague?
Your responsibilities as a Regulatory Affairs Advisor
You will join an exciting, international advisory department with highly skilled colleagues that have a deep understanding of the life sciences industry and the ability to bridge this knowledge with digital technologies such as machine learning and Cloud solution such as Veeva Vault.
Working closely with international clients, you will use your experience from Regulatory Affairs to advise and assist companies in a vast array of projects, spanning from RA process optimization to new regulatory changes. You will be expected to advice clients on vendor selections for new IT solutions within the area of electronic document management systems (EDMS), eCTD, labelling and regulatory information management systems (RIMS), including IDMP. You may also have knowledge of Pharmacovigilance or Medical Devices processes and systems.
A key part of the job is business development activities related to new offerings that will support our continued growth within the areas of Regulatory Affairs. The job will include close collaboration with a multitude of stakeholders within NNIT where your specialist knowledge will strengthen our companies' strategic aspirations in Regulatory Affairs. You will also be expected to give presentations and speaker sessions at conferences and write articles about Regulatory Affairs topics.
You will be part of NNIT’s Life Sciences Advisory
NNIT’s Life Sciences Advisory is an ambitious department with a key importance to NNIT’s strategy. We appreciate openness, honesty and a winning attitude.
Our customers expect us to know about upcoming trends and regulatory changes, as well as they expect us to be at the forefront in terms of technical solutions. Your career will include continuous training and competence development to support our department and your personal ambitions.
NNIT was recently nominated as the most attractive workplace within the IT consulting area in Denmark.
Your qualifications and experiences
You hold an MSc degree in Life sciences or IT with 3-5 years of experience from the life sciences industry (preferably Regulatory Affairs). You have a strong understanding of IT, and you manage to bridge your professional experience from the life sciences industry with IT. You must have a curious nature and interest in new technologies.
It is an advantage if you have experience with business processes and regulatory requirements within Regulatory Affairs and that you have a good overall understanding of IT solutions within this area.
You are used to advice and build trust on all levels, and you might have gained this experience from a past job within the consulting area. NNIT has offices in Copenhagen, Frankfurt and Basel, and we will expect you to live in the proximity of these pharma hubs.
Fluency in oral and written English is a must. German or Danish is beneficial. Travel must be expected.
Information og data
Denne ledige stilling har jobtypen "Apoteker", og befinder sig i kategorien "Sundhed og forskning".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 10.8.2020, 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
- Søborg
- Mandag den 31. august 2020
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