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Are you motivated by the opportunity to influence and improve the environmental performance of water companies?. You will increase the effectiveness of our evidence based communications to protect and improve the environment for people and wildlife. Ability to work under own initiative in a disperse

The Director, Manufacturing and Site Lead role at LGC offers a chance to lead in innovative manufacturing in a dynamic setting. Lead manufacturing teams and site administration to ensure compliance with applicable quality, safety, and regulatory standards. A minimum of a decade of experience within

Collaborate with Senior VP Regulatory Sciences to develop and execute global regulatory strategies with Global Regulatory Leads for all products. Global regulatory leads, head of regulatory operations, tactical implementation team, and lead of Regulatory/Medical Writing will report to this role. The

As Associate Director, Global Regulatory Science – CMC, you will lead regulatory CMC strategy and execution for one or more mRNA programs. Support cross‑functional collaboration and embed a global regulatory mindset into CMC initiatives. You will operate at the cutting edge of regulatory science

Regulatory Affairs manager – Medical Devices. Regulatory Affairs manager – Medical Devices. A new role in Regulatory Affairs has become available at an exciting medical devices organisation with products undergoing clinical trials.

VP Global Regulatory Affairs / Regulatory Affairs / Advanced Therapy / Gene Therapy / Biologics / ATMP / CGT / CDMO / CMC / FDA / EMA / MHRA / Leadership / Compliance / Regulatory Strategy / Quality Systems / Biotechnology. To be successful in your application to this exciting role as the VP, Global

The Regulatory Affairs Analyst and Competition Policy Analyst is an exciting role in the Legal and Corporate Affairs (LAC) team providing senior level advice relating to antitrust, litigation, regulation, and M&A. We’re looking for a Regulatory Affairs Analyst and a Competition Policy Anal