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legal engineer, government & jobs near stuvsta

VIE - Medical Information and Quality Nordic & Baltics

Ipsen Pharma (SAS) -
Stockholm

Ansök nu

Jobbinformation

Heltid

Kvalifikationer

Franska
Engelska
Masterexamen
Organisationsförmåga
Farmaci och farmakologi

Fullständig jobbeskrivning

V.I.E (Volontariat International en Entreprise) is a program run by Business France, the French government agency. It allows young professionals from the European Economic Area to work for a French company outside of France for a limited period. Participants are not Ipsen employees but have a special V.I.E status.

To take part in the program, there are specific eligibility criteria that must be met and will be verified by Business France. Those who do not meet the eligibility criteria cannot be part of this program but can apply to other opportunities within Ipsen.

***********************

Location : Stockholm, Sweden

Duration : 18 months

At Ipsen, we are a global biopharmaceutical company focused on bringing innovative medicines to patients in oncology, rare diseases and neuroscience. We are looking for a motivated and scientifically minded VIE to join our Nordic Medical team and support both Medical Information and quality activities across the Nordics & Baltics.

This is a unique opportunity to gain exposure to Medical Affairs, Quality, Regulatory and cross-functional collaboration within an international healthcare environment.

Your Key responsibilities

Medical Information

Provide accurate, balanced and timely medical information to healthcare professionals and internal stakeholders.
Support medical information activities across Sweden, Norway, Denmark, Finland, Estonia, Latvia and Lithuania.
Conduct scientific literature searches and summarize key medical insights.
Maintain and update standard response documents and medical information content.
Support the administration and optimization of medical information systems and databases.
Collaborate closely with Medical Affairs, Pharmacovigilance, Quality, Regulatory Affairs and Commercial teams.

Quality & Regulatory Support

Support artwork reviews and quality checks.
Assist with regulatory dossier management activities.
Participate in the management of product quality complaints.
Contribute to KPI reporting and training administration activities.
Support GDP compliance and continuous quality improvement initiatives.

About you

Master's degree or higher in Pharmacy, Life Sciences, Medicine or a related scientific discipline.
Strong scientific mindset with the ability to analyze and communicate complex medical information.
Excellent written and verbal communication skills in English.
Highly organized, proactive and comfortable working in a dynamic international environment.
Interested in Medical Affairs, Quality and Regulatory Affairs within the pharmaceutical industry.
Previous experience in Medical Information, Quality or Regulatory Affairs is a plus.

Why Ipsen

You'll gain valuable international experience, work with experienced professionals across multiple countries, and contribute to improving patient care through scientific excellence and quality.

We are committed to creating a workplace where everyone feels heard, valued, and supported; where we embrace “The Real Us”. The value we place on different perspectives and experiences drives our commitment to inclusion and equal opportunities. When we include diverse ways of thinking, we make more thoughtful decisions and discover more innovative solutions. Together we strive to better understand the communities we serve. This means we also want to help you perform at your best when applying for a role with us. If you require any adjustments or support during the application process, please let the recruitment team know. This information will be handled with care and will not affect the outcome of your application.

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