About Freyr Freyr is a fast-growing, innovative company specializing in providing end-to-end regulatory solutions and services for the Life Sciences industry. With a commitment to excellence and innovation, we assist pharmaceutical, medical device, and biotech companies in navigating the complexities of regulatory compliance.
At Freyr, we believe in fostering a collaborative and dynamic work environment that empowers our team to make a real impact. As we expand our footprint, we are on the lookout for passionate and skilled Regulatory professionals to join us in shaping the future of regulatory services.
If you're ready to embark on a journey of growth and innovation, connect with us to explore the exciting opportunities awaiting you at Freyr. Together, we can shape the future of regulatory solutions.
Don't miss this chance to be a part of Freyr's expansion and make your mark in the world of regulatory services. Let's redefine regulatory excellence together!
Title : Regulatory Project Manager
Location : Remote ( Base location should be in EU, preferably in UK/ Hungary/ Poland / Romania/ Czech/ Croatia)
Experience : 5 years in Medicinal Products Regulatory Affairs with 2 years in Project Management.
PM experience - MS Projects
SWG Meeting management( Driving cross functional Team meetings)
Submission Working Groups (SWG) management of –
Detailed Regulatory Timelines
Risks, Actions, Issues, Decisions (RAID) log
Global Regulatory Teams (GRT) management of -
Regulatory Project Plan (RPP)
Risks, Actions, Issues, Decisions (RAID)
Bachelor’s degree in Pharma / Medical or another associated scientific discipline OR equivalent
# 4 years of experience in the Regulatory field and 2 years of demonstrated project management skill sets ( required )
# Experience working with Microsoft Project or equivalent program ( preferred ).
# Excellent business collaboration/interpersonal skills.
# Intermediate proficiency in Microsoft Office products such as Word, Excel, and Outlook.
# Fluency in English (written, verbal, reading).