This position is suitable for a Chemistry or Science Graduate who has an interest and desire to work in a regulatory / quality compliance role in the Chemical, Pharmaceutical and Personal Care industries.
Our Client is a Chemical Distributor.
This position will be office based near Bracknell, Berkshire and is a full-time permanent role.
The Regulatory Associate is responsible for providing global regulatory expertise for Clinical Trials.
They are the primary interface between global functions and affiliates to deliver clinical development regulatory strategies, operations and outcomes.
General
SRG are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office in Maidenhead/Remote.
Fabulous Health and Wellness company are looking for an experienced Senior Regulatory Affairs Associate to play a pivitol role in an exciting new project focused on developing a comprehensive product claims database.
IDEALLY HAVE FOOD SUPPLEMENT, MARKETING EXPERIENCE, HAVE EXPERIENCE IN FOOD SAFETY, LEGISLATION, NUTRITION.
This well-known biopharmaceutical company is looking for a Regulatory Affairs Labelling Associate Project Manager to join their Labelling team on a contracting basis.
Your new company.
This is a 12-month contract job with scope for extension and is fully remote.
A Regulatory Specialist is urgently required or the responsibility of ensuring the company complies with Global Chemical Regulations in the markets and territories it operates within.
I am looking for a experienced, client facing Regulatory Risk Associate Director for a international, market leading client.
You will be based in their London office and be engaged in providing guidance, pragmatic advise and insight in to their clients regulatory and risk issues.
My client works with global financial institutions from investment and wholesale banks, asset managers and insurers.
An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU and early stage development experience to join their team on a 12 month temporary contract.
Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance across the region and make sure that regulatory deadlines and approvals are achieved.
Other responsibilities include
You will develop, contribute and ensure the accurate preparation of high-quality regulatory documents needed to support clinical trials and medical products.