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Apsida Life Science

Verified Job SourceRecruitment agency

Specialist Global Leaders in Life Science Recruitment: Empowering Life Science innovation with integrity.

Surrey, England

Staffing and Recruiting
11–50 people

About

Founded in 2019, Apsida Life Science is a specialist recruitment business Headquartered in Surrey, with offices in London UK, Boston USA and Pretoria, SA. Leveraging our inch-wide, mile-deep networks we’re expertly placed to support your hiring needs across the CRO, Pharmaceutical, Biotechnology, Medical Device, CDMO, eClinical, Patient Recruitment & DCT space. We recognised the opportunity to provide a recruitment service that delivers genuine value and exceptional experiences through bespoke, cost-effective solutions grounded in quality and integrity. We build lasting relationships by earning trust through transparency and consistency, utilising our expansive network and deep industry knowledge. Rather than focusing solely on transactions, we guide clients and candidates through every stage of the hiring process, offering strategic insights and tailored support. _________________________________________________ Listen to Apsida Insights Podcast on Spotify, Apple Podcasts & watch on YouTube. The podcast that takes you inside the world of life science. We bring you exclusive conversations with industry leaders, deep dives into market trends, and discuss career growth, hiring strategies, and international expansion.

Open positions

CMC Regulatory Consultant

Remote · Canada

Review CMC regulatory documentation and provide hands-on support with Module 3 materials, including identifying gaps and supporting submission readiness. Draft, review, and update SOPs in response to Health Canada guidance, collaborate with the client's CMC colleague, and assist with additional regulatory tasks.

Senior Regulatory Affairs Consultant

Remote · Canada

Review CMC regulatory documentation and provide strategic expertise, while drafting and updating SOPs based on Health Canada guidance and regulatory changes. Support the client’s CMC team in preparing and finalizing CTD Module 3 documentation, and provide additional short-term regulatory support as needed.