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As a Senior Manager, Regulatory Affairs CMC, you are an integral part of MoonLake’s Clinical Development team responsible for the development, execution and tracking of regulatory CMC and medical device activities.
You will be responsible for the development of a CMC and device regulatory strategy, working closely with Technical Operations colleagues. The Senior Manager, Regulatory Affairs CMC will serve as a subject matter expert, which will involve collaborating with multiple internal and external partners and will ensure adherence to relevant regulatory requirements.
Key Responsibilities:
Education:
MoonLake Immunotherapeutics is a clinical-stage biopharmaceutical company unlocking the potential of sonelokimab, a novel investigational Nanobody® for the treatment of the inflammatory disease, to revolutionize outcomes for patients.
We continue to make significant progress in our Global Clinical Development Programs. The company’s focus is on inflammatory diseases with a major unmet need, including hidradenitis suppurativa and psoriatic arthritis – conditions affecting millions of people worldwide with a large need for improved treatment options. MoonLake was founded in 2021 and is headquarted in Zug, with hubs in Cambridge & Porto.
Further information is available at
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The work culture at MoonLake Immunotherapeutics must adhere to the Ethics of Work Culture as described in the Ethical framework of the UN Charter. You can gain more insights into their local workplace environment by exploring their jobs MoonLake Immunotherapeutics and also by visiting their official website through Google.
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Yes, we found live job(s) for MoonLake Immunotherapeutics in Cambridge.
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