Open Permanent Positions

Our client is a clinical stage biopharmaceutical company which is utilizing a novel Artificial Intelligence platform to identify and develop medicines for neuropsychiatric indications.  They are seeking a Vice President of Regulatory Affairs (or Executive Director) who can develop and lead clinical

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This company is a global leader in advanced molecular testing solutions. They are seeking a Regulatory Affairs Director who can lead global regulatory strategies for a portfolio of IVD products and manage a small team.  You will provide regulatory guidance to internal teams, while also interfacing

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This successful biopharma company develops and commercializes innovative cancer immunotherapies. They are seeking a Regulatory Affairs Senior Manager who can contribute to regulatory strategies for multiple novel immune-oncology programs.  You will work closely with cross-functional teams to advanc

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This growing company is developing innovative RNAi-based therapeutics for the treatment of rare diseases.  They are seeking a Regulatory Strategy Director or Senior Director to develop and implement global regulatory strategies for their early-stage programs. You will be responsible for the prepara

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This biotech startup is developing gene therapies for people with rare, devastating diseases.  They are seeking a Head of Regulatory Affairs who can lead their Regulatory function and file their first IND.  You will develop and execute regulatory strategies for AAV gene therapy programs and build

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This company is a global leader in advanced molecular testing solutions. They are seeking a Regulatory Affairs Senior Manager who can develop and manage global regulatory strategies and filings for a portfolio of IVD products.  You will lead the preparation and submission of regulatory applications

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This company is a global leader in advanced molecular testing solutions. They are seeking a Regulatory Affairs Manager who can lead commercial regulatory activities for approved IVD products.  This includes promotional review, labeling, and other regulatory filings. You will work closely with Marke

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This innovative diagnostics company develops automated IVD solutions for molecular testing. They are seeking a Regulatory Affairs Manager who can develop regulatory strategies and provide regulatory guidance for a portfolio of IVD products.  You will lead the preparation and submission of regulator

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This innovative diagnostics company develops automated IVD solutions for molecular testing. They are seeking a Regulatory Affairs Specialist to coordinate regulatory submissions with the FDA and EU for their IVD products. You will maintain technical files and regulatory documentation and support pro

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This innovative diagnostics company develops automated IVD solutions for molecular testing. They are seeking a Regulatory Affairs Senior Specialist to work on regulatory submissions with the FDA and EU for their IVD products. You will reviewing technical reports, labeling and advertising material fo

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This San Diego biopharma company specializes in identifying, developing and delivering life-changing therapies to people living with rare disease. They are seeking a Regulatory Affairs Senior Director who can develop and lead global regulatory strategies for approved products and programs in develop

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This San Diego biopharma company specializes in identifying, developing and delivering life-changing therapies to people living with rare disease. They are seeking a Regulatory CMC Director to lead their CMC Regulatory function globally and manage one direct report.  You will develop global CMC str

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This small, clinical stage pharmaceutical company is developing life-changing therapies for genetic diseases.  With their lead candidate for DMD in Phase 3, they are seeking a Regulatory Affairs Manager to join their growing team.  You will contribute to and execute upon global regulatory strategi

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This client develops, manufactures, and markets a broad range of innovative diagnostic products. They are seeking a Regulatory Affairs Manager who can manage a small team of Regulatory professionals and oversee regulatory submissions for pre-market IVD products. You will work closely with cross-func

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This San Diego biotechnology company is focused on novel biological and drug delivery technologies.  They are seeking a Regulatory CMC Director that can develop and execute on regulatory CMC strategies for assigned partner programs, and manage junior-level staff. You will work closely with cross-fu

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This small but growing Bay Area pharmaceutical company has one approved product and a very strong pipeline of novel therapeutics for the treatment of rare diseases.  They are seeking a Regulatory Affairs Director or Associate Director that can contribute to and execute on regulatory strategies for

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This Bay Area pharmaceutical company is developing and commercializing innovative therapies for women's health and prostate cancer.  With the anticipated FDA approval of two NDAs this year, they are growing rapidly and expanding their team.  They are seeking a Clinical Regulatory Affairs Director

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This Bay Area pharmaceutical company is developing and commercializing innovative therapies for women's health and prostate cancer.  With the anticipated FDA approval of two NDAs this year, they are seeking an Associate Director or Director of Commercial Regulatory Affairs who can review and approv

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This San Diego biotechnology company is focused on novel biological and drug delivery technologies.  They are seeking a Regulatory CMC Director that can develop and execute on regulatory CMC strategies for assigned partner programs, and manage junior-level staff. You will work closely with cross-fu

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This client is one of the largest contract manufacturers of biologics in the world.  Due to a significant expansion at their Portsmouth site, they are seeking a Regulatory CMC Manager (or Sr. Associate) to provide regulatory support for multiple client projects.  In this role you will contribute t

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This global pharmaceutical company is seeking a Senior Director, Regulatory Team Leader to oversee its Rare Disease portfolio.  In this role you will provide strategic input into US and global regulatory strategies, while leading a team of direct reports.  You will also serve as the primary contac

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