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