Auftragsdetails

Consultant, Regulatory Sciences - propharma group

Datum der Veröffentlichung: Mar 27, 2023
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Auftragsdetails

  • Ort:
    Stockholm, Stockholm, Sweden
  • Gesellschaft:
  • Typ:
    Full Time/Permanent
  • Shift:
    First Shift (Day)
  • Karrierelevel:
    Experienced Professional
  • Positionen:
    4
  • Erfahrung:
    2 Year
  • Geschlecht:
    Keine Präferenz
  • Grad:
    Masters
  • Vorher bewerben:
    Nov 30, 2023

Job Summary

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.

Detailed Description

ProPharma Group Sweden is located in central Stockholm with a smaller site in Malmö, south of Sweden. As a result of the continuous growth of our company, we are now looking to recruit a Regulatory Affairs Consultant to our Regulatory Affairs Division. Location could be either Stockholm or Malmö.

 

In the role as Regulatory Affairs Consultant you will be working on projects from a variety of Pharmaceutical, Biotechnology and Medical Device companies. On 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.

 

The work may include, but is not limited to:

  • Working with Regulatory Affairs, primarily on a local level, with focus on the Nordic countries (Sweden, Denmark, Norway, Finland and Iceland).
  • Regular contact with health authorities
  • Regulatory intelligence
  • Local regulatory advice
  • New registrations/variations/MAH-transfer applications
  • Launch preparations
  • Local database updates
  • Update/translation of product information
  • Review of artwork
  • Updates to compendiums.

 

The position can be based either in Stockholm or in Malmö.

 

Qualifications

  • 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.
  • 2-3 years of experience in Regulatory Affairs.
  • MSc in Pharmacy, or equivalent.
  • Excellent communication skills (oral and written) in one or several Nordic languages and English language

 

All candidates must be legally eligible to work in Sweden.

 

***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.

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Company Overview

Berlin, Berlin, Germany

ProPharma Group is the leading global, independent, single-source provider of regulatory, clinical, and compliance services serving the pharmaceutical, biotechnology, and medical device companies. Our team of experts brings a comprehensive portfolio... Read More

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