Regulatory Affairs Specialist

2 weeks ago

Cambridge, United Kingdom VRS Regulatory Full time

An excellent opportunity to join a well-established regulatory consultancy that is just entering a period of sustained growth. They have a large range of clients including SMEs and multi-nationals; they act as outsourced regulatory department for some clients and have projects of all sizes with a EU wide portfolio. The roles are delivery focussed, there is no pressure to win new business, you will be concentrating on delivery of registration and risk assessment projects.

They are looking for a regulatory officer/specialist with biocide experience - this is a hands-on delivery role preparing registration dossiers, gathering data, commissioning studies etc. They offer excellent on-going training and development.

This role would be ideal for a 2nd or 3rd career move - you are likely to have 2-5 years’ experience in biocide regulatory affairs - this could be with another consultancy or a manufacturer. The roles are very flexible on location, you can be remotely based, work on a Hybrid basis or from the offices. They will also consider full and part-time.

**Key Skills**: Regulatory affairs, registrations, dossiers, data gap analysis, products, substances, active ingredients, study monitoring, data gathering, report writing, study summaries, waivers, generalist, specialist, biocides, biocidal products, BPR

**VRS Regulatory** is the Regulatory Affairs and Risk Assessment division of specialist scientific recruiter VRS. We focus on recruitment in Regulatory Affairs, Registrations, REACH, CLP, SDS Authoring, Product Safety, Compliance, Risk Assessment, Regulatory Toxicology, Regulatory Ecotoxicology and Environmental Fate in the chemicals, agrochemicals and biocides sectors.

**Benefits**:

- Work from home

Schedule:

- Monday to Friday

Reference ID: VRSREG1898

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