MoonLake Immunotherapeutics

1-20

FTE

MoonLake Immunotherapeutics AG is pioneering advanced medicines utilizing innovative Nanobody® technology to tackle immunologic disorders, particularly in inflammatory skin and joint diseases.

MoonLake Immunotherapeutics AG is a dynamic clinical-stage biopharmaceutical firm dedicated to harnessing cutting-edge Nanobody® technology. The company focuses on developing transformative therapies for immunologic conditions, with a specific emphasis on inflammatory skin and joint diseases. With a commitment to innovation and excellence, MoonLake is poised to make significant strides in the biopharmaceutical landscape.

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Funding

€104.55M

HQ City

Zug

Revenue Model

B2B

Employee Count

1-20

Last Funding Round

06/2023

Stage

Late

Team Growth

-4%

YoY Website Traffic Growth

58%

Manager Quality GCP Compliance

MoonLake Immunotherapeutics

MoonLake Immunotherapeutics AG is pioneering advanced medicines utilizing innovative Nanobody® technology to tackle immunologic disorders, particularly in inflammatory skin and joint diseases.

MoonLake Immunotherapeutics AG is pioneering advanced medicines utilizing innovative Nanobody® technology to tackle immunologic disorders, particularly in inflammatory skin and joint diseases.

Porto

Munich

• Senior-Level

• Hybrid

• Finance/Legal & Compliance

2025-05-29 0:03:10

2025-05-29 0:03:10

About Company
About Company
About Company

TL;DR

TL;DR
✨ The Role in One Sentence

MoonLake is seeking a Senior Manager Quality GCP Compliance to ensure robust GCP quality oversight across clinical programs and vendors.

📋 What You'll Likely Do
  • 30%: Support implementation and delivery of GCP Quality oversight requirements within MoonLake and its vendors.

  • 30%: Serve as GCP Subject Matter Expert, providing independent quality guidance to assigned clinical trial teams.

  • 40%: Support GCP inspection readiness activities and management of regulatory inspections of MoonLake.

🧑‍💻 Profiles Doing This Job
  • High Priority: Comprehensive (8+ years) experience in Clinical Quality Assurance and/or Clinical Operations.

  • High Priority: Substantial knowledge of Good Clinical Practice (GCP) requirements across all phases of clinical development.

  • High Priority: Experience conducting GCP clinical audits.

📈 How This Role Will Look on Your CV
  • Ensured GCP compliance across clinical programs and vendors in a biotech environment.

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