Job Openings Regulatory Specialist

About the job Regulatory Specialist

Job Title: Regulatory Specialist

Job Location: Ashington, UK

Job Location Type: Hybrid

Job Contract Type: Full-time

Job Seniority Level: Entry level

About

The Company

Our client is a specialist in the manufacturer for the pharmaceutical sector. Due to growth, they are now looking to recruit a Regulatory Specialist.

The Role

  • Manage and maintain EU, GB and EMEA authorisations of biocidal products; ensure compliance with other chemical regulations where applicable e.g. CLP; manage and maintain transitional biocidal registrations.
  • Submission, maintenance, changes and renewals for products under EU BPR, GB BPR and other EMEA regulations as per market requirements.
  • IUCLID dossier build, use of R4BP, preparation of SPCs, submission of IUCLID dossiers, preparation and submission of Poison Centre Notifications.
  • Supporting Quality Assurance with implementing regulatory changes e.g. label artwork and Change Controls.
  • Providing regulatory input for SDS preparation, marketing, sales, technical and R&D.
  • Attend regulatory meetings in EU and elsewhere as required.
  • Regulatory monitoring, including awareness of new regulations and changes to existing regulations, including internal communication of any potential impact to the company.
  • Maintain compliance with other chemical regulations e.g., REACH, CLP, Detergents, as applicable for product range.
  • Submission of annual biocidal product sales quantities to selected Member States.
  • Liaise with all departments, project teams, suppliers, testing laboratories, distributors, consultants and Member State Competent Authorities to co-ordinate and monitor regulatory submissions and requirements
  • Support other group sites with global disinfectant registrations.
  • Could be full time or part time depending on the person.
  • Could also offer remote working but site visits at least once a month or expected.

The Person

  • Will have experience within a similar role.
  • Must have biocides and BPR experience.
  • You will have good IT Skills (Word, PowerPoint and Excel).
  • Be proficient in use of IUCLID and R4BP.
  • Good scientific communication (written and oral).
  • Experience with human health toxicology and environmental risk and exposure assessments would be desirable.
  • Experience with efficacy testing for regulatory purposes is desirable.
  • Experience with CLP, REACH, SDS authoring and regulatory labelling would be beneficial.

The Benefits

  • Discretionary annual bonus.
  • Private Medical Insurance for you and your family.
  • Pension Scheme.
  • Corporate benefits platform and Cycle to Work Scheme.
  • Death in Service Benefit.
  • Remote or part time working.

TITL1_UKTJ

  • Ashington, England

Languages

  • English


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