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Biocides Regulatory Affairs Manager

Kenton Black
Job LocationChester
EducationNot Mentioned
Salary£40,000 - £50,000 per annum, inc benefits
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent, full-time

Job Description

Biocides Regulatory Affairs Manager (AH006)Location: Chester, Cheshire£40K - £50K Basic + 25 Days Holiday + Bonus Scheme + Share Options + 5% Matched Pension + Flexible Working OptionsOur client is a market-leading healthcare business who manufacture a huge range of infection control products. They are an organisation who pride themselves on employee career progression which, coupled with significant future investment into the Regulatory Affairs team, will offer many opportunities for the right individual.Recognised as a leading manufacturer in their field, they have seen huge growth over the last 12 months and are looking to recruit a Biocides Regulatory Affairs Manager to continue to drive this impressive growth.Role ResponsibilitiesAs a Biocides Regulatory Affairs Manager, you will be responsible for:

  • Ensuring regulatory compliance of new products being developed by R&D
  • Controlling regulatory compliance of existing products
  • Compiling product dossiers for submission in line with Biocidal Product Regulations (BPR)
  • Interacting regularly with regulatory bodies including HSE
  • Networking at seminars to increase market knowledge
  • Keeping abreast of any changes to BPR
  • Being the Biocides SME in the business and providing technical expertise to senior management
  • Liaising with a multitude of departments within the business including Sales, Marketing, Supply Chain and R&D
  • Working alongside the Medical Devices Regulatory Affairs Manager to share knowledge and ideas.
    • Role RequirementsTo be successful in this role, you will have proven experience in a regulatory affairs or product safety / product stewardship role in a detergents / biocides / healthcare company; and therefore possess extensive knowledge of Biocidal Product Regulations (BPR).Experience with product dossier submissions is essential - ideally, and more specifically, previous experience with dossier compilation too.You will be degree-level qualified (or equivalent) in Chemistry or a closely related subject, with the ability to communicate effectively at all levels.Keywords: Regulatory Affairs, Regulatory, Regulatory Compliance, Regulations, Biocides, BPR, Biocidal Product Regulations, Dossier, Healthcare, Med Device, Medical Device, ISO13485, ISO 13485. Required skills
  • Biocides
  • Regulatory Affairs
  • Dossiers

    • Keyskills :
    Biocides Regulaty Affairs Dossiers

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