Biocide Regulatory Specialist – National/Transitional dossiers

JR United Kingdom; Preston; On-site; GBP 25,000 - 35,000; Full time

Job summary

A leading company in the manufacturing of disinfectant products offers an opportunity to join their EU Regulatory Affairs team. The role involves preparing regulatory dossiers for biocide products, collaborating closely with an experienced regulatory manager. Ideal candidates will have 1-2 years of experience in regulatory affairs with biocides, demonstrating their capability to produce detailed submissions for compliance.

Qualifications

• 1-2 years’ experience in regulatory affairs, ideally with biocides.
• Experience in dossier preparation for plant protection products, chemicals, or cosmetics is a plus.
• Not suitable for complete beginners; some regulatory experience required.

Responsibilities

• Preparing dossiers for biocide products via national notifications to EU countries.
• Collating and reviewing data, checking stability and efficacy studies.
• Passing dossiers to partner organisations for submission to authorities.

Skills

Regulatory Affairs

biocides

regulatory submission

dossier preparation

data gathering

collation

compilation

national product notifications

Job description

Social network you want to login/join with:

col-narrow-left

Client:

VRS Regulatory

Location:

preston, lancashire, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

col-narrow-right

Job Views:

4

Posted:

31.05.2025

Expiry Date:

15.07.2025

col-wide

Job Description:

An opportunity to join the EU Regulatory Affairs team at a global disinfectant products manufacturing company. You will work alongside an experience regulatory manager who will provide training where needed; your role will be to work on preparing dossiers for biocide products via the national/transitional notifications to EU countries.

This role will focus on dossier preparation for disinfectants (PT2, 3, 4 & 5); you will collate and review data, check the studies e.g. stability, efficacy, method of analysis etc, pull the dossier together and pass on to the partner organisation who will submit to the relevant country authority. You will focus on EU countries.

We are looking for someone with 1-2 years’ experience in regulatory affairs – ideally with biocides; experience of pulling together data for dossiers for other product types would also be of interest eg PPP (plant protection products), chemicals (REACH) and cosmetics (preparing PIFs) – this is not a role for a complete beginner – you must have some regulatory/dossier preparation experience.

Key Skills: Regulatory Affairs, biocides, regulatory submission, biocidal products, dossier preparation, data gathering, collation, compilation, national product notifications.

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.