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GSK remains committed to achieving bold commercial ambitions for the future. By 2031, we aim to deliver £40 billion in annual sales, leveraging our existing strong performance momentum to significantly increase our…
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for…
A QA specialist at GE Healthcare ensures product quality by handling deviations, CAPAs, complaints, and SOPs while supporting projects and cross-functional teams in a fast-paced environment. Core tasks include GMP compliance, batch documentation, and problem-solving for pharmaceutical manufacturing and regulatory processes.
Parexel is seeking experienced CMC (Chemistry, Manufacturing, and Controls) professionals to join us as a Regulatory Affairs Consultant CMC Author to support our client. This position requires expertise in regulatory…
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice…
Senior Technical Product Analyst on Merck's RDLM Product Team, bridging business and IT to deliver regulatory document lifecycle management capabilities—gathering requirements, analyzing processes, and supporting delivery using JIRA and Veeva RIM in a regulated pharma environment.
An entry-level intern supporting senior analysts with data management, analytics, and reporting tasks using SQL Server, Power BI, Excel, and MDM tools.
At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop,…
Review and approve batch records and technical documentation for biological products in a GMP-regulated environment, ensuring compliance with USDA, FDA, and EU regulations; uses SAP, Veeva, and Microsoft Suite.
At Elanco (NYSE: ELAN) – it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At…
Whether it's the unique breadth of our integrated offering that covers Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology products; or our commitment to recognizing and rewarding people for…
Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full…
Title: Senior Manager, Medical Communications & Publications Company: Ipsen Biopharmaceuticals Inc. About Ipsen: Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in…
Who We Are: Neurocrine Biosciences is a leading biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering, developing and commercializing…
When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every…
About the Role We are seeking an experienced Regulatory Affairs professional to lead IVD (in vitro diagnostic devices) regulatory strategy. In this pivotal role, you will provide expert guidance on regulatory pathways…
About the Role We are seeking an experienced Regulatory Affairs professional to lead medical devices and combination products regulatory strategy. In this pivotal role, you will provide expert guidance on regulatory…
COMPANY: At BioCryst, we share a deep commitment to improving the lives of people living with hereditary angioedema (HAE) and other rare diseases. We leverage our expertise in structure-guided drug design to develop…
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