Regulatory Project Manager

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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.
Why Freyr?
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.
Join Our Team:
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.
? To Apply:
Please apply to this job post or you can visit our Careers page for more openings
Visit our Careers page at (https://www.freyrsolutions.com/careers/current-positions) to explore current job openings and submit your application.
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.
Must have experience:
US / EU Major submissions Experience
Hands on exp with IND/NDA/BLA
PM experience - MS Projects
SWG Meeting management( Driving cross functional Team meetings)
Key Responsibilities:
Submission Working Groups (SWG) management of –
SWG Kick Off Meetings
Recurrent SWG Meetings
Detailed Regulatory Timelines
Risks, Actions, Issues, Decisions (RAID) log
Rapid Response Team (RRT)
Lessons Learned log, as applicable
Global Regulatory Teams (GRT) management of -
Meetings support, as required.
Regulatory Project Plan (RPP)
GRT Goals
Risks, Actions, Issues, Decisions (RAID)
Independently leading additional Non-SWG submission types
Requirements:
Bachelor’s degree in Pharma / Medical or another associated scientific discipline OR equivalent
Min. 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 ).
Experience in driving/supporting submissions for major markets - US, EU, etc. (e.g. IND, NDA, BLA, EU MAA, EU variations, etc.) would be preferred.
Strong conceptual and analytical thinking skills.
Ability to work under deadlines and fast-paced work environment.
Excellent business collaboration/interpersonal skills.
Intermediate proficiency in Microsoft Office products such as Word, Excel, and Outlook.
Ability to multitask and prioritize competing assignments.

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