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Join our mission to close in on cancer.
As a member of our CMC (Regulatory Affairs) team, you will play an important role in managing, writing, preparation, and review of RA-CMC regulatory filings for submissions of Merus’ product candidates in compliance with the applicable regulatory and quality requirements. You will also provide biopharmaceutical CMC-content related regulatory advice to the rest of the CMC team.
As Regulatory Affairs CMC Officer, your main tasks and responsibilities are the following:
Managing the communication and follow-up with Competent Authorities on CMC regulatory related feedback received.
We are looking for a Regulatory Affairs CMC Manager with the following knowledge and expertise:
We offer a once-in-a-lifetime opportunity to work with some of the best and brightest in the biotech industry. As part of Merus, you’ll experience a steep learning curve from your very first day in the job. And you’ll get to interact with a great international team of people who love what they do! To top it all, we offer a competitive salary, flexible working hours, an excellent pension scheme, a company bonus, and 30 days’ annual leave (based on a full-time position). Most importantly, you’ll have the chance to help us close in on cancer – everything you do matters at Merus.
At Merus, we are clinically advancing leading-edge, targeted treatments to address the unmet needs of patients with various types of cancer. Utilizing our proprietary technology platforms, we are developing innovative multispecific antibody therapeutics, referred to as Multiclonics.
Deze bedrijfspagina is automatisch gegenereerd en bevat daarom nog weinig informatie. Je vindt meer informatie over ‘bedrijfsnaam’ op hun website: ‘’Carrierewebsite’’
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