Senior Regulatory Affairs Consultant
Altran Sverige AB / Administratörsjobb / Stockholm
2021-02-17
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➡️ Klicka här för den senare publicerade platsannonsen "Senior Regulatory Affairs Consultant" (publicerad 2022-11-15) ⬅️
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hela Sverige Our offer
Altran offers you a work environment that is characterized by innovation. As a consultant at Altran, you are part of something bigger.
The assignments are mainly at customer's sites but also in the form of internal projects. In our Life Sciences division, which in Stockholm consists of approximately 15 employees, we have a wide range of different competencies represented, which gives you good opportunities to learn from your colleagues.
Great atmosphere and present managers who have their main task to facilitate and work closely with the consultants, are all in line with Altran's values - Ambition & Care.
We care about you as a colleague and offer you a safe and favorable employment. For us, community is important and in addition to professional development, we offer you a variety of activities. We work to promote participation by continuously arranging lunches, breakfasts, After Works, sports events and more.
In the role as Senior Regulatory Affairs Consultant you will be working in a variety of Life Science projects. In the projects you will be dealing with challenging and varied tasks that requires you to be result and client orientated and to display excellent interpersonal skills. At the same time you will have the opportunity to actively participate in the company's continued development.
Your role
Working operationally and strategically with Regulatory Affairs, both at a local and global level.
In projects, provide regulatory expertise and guidance on procedural and documentation requirements.
Be the regulatory advisor for new product registrations/variations/renewals and launch preparations.
Identify potential regulatory risks and propose options to mitigate these.
Regular communication with health authorities and regulatory intelligence
Function as the Regulatory expert in inhouse projects at Altran.
Your profile
MSc in Pharmacy or Engineering
At least 5 years of experience in Regulatory Affairs from the Life Sciences industry
Excellent understanding of registration procedures and requirements as well as product life cycle management from regulatory affairs perspective.
Strong project management skills.
Having an open eye for the needs of your customers and the ability to adjust to these needs.
Able to work to deadlines and solving issues in a pragmatic and proactive way
Ensuring you are able and willing to dig into the details yet keeping an eye on the overall goal of the project.
Fluent in Swedish and English language.
Feel free to apply through our website
www.altran.com or through Linkedin. For questions, please reach out to Anette Nilsen, Talent Acquisition Partner, 073 025 05 17,
anette.nilsen@altran.comPubliceringsdatum2021-02-17Så ansöker duSista dag att ansöka är 2021-03-19
Klicka på denna länk för att göra din ansökanAdressAltran Sverige AB
Holländargatan 10
11136 Stockholm
Omfattning Detta är ett heltidsjobb.
Arbetsgivare Altran Sverige AB (org.nr 556542-2531)
Holländargatan 10 (
visa karta)
111 36 STOCKHOLM
Jobbnummer 5582090
Observera att sista ansökningsdag har passerat.