Regulatory Affairs Specialist Hybrid - London, United Kingdom - PE Global

PE Global
PE Global
Verified Company
London, United Kingdom

1 month ago

Tom O´Connor

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Tom O´Connor

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Description

PE Global is currently recruiting for a Regulatory Affairs Specialist for a leading multi-national Biotech client based in London (hybrid)


This client's Regulatory Affairs team manages a broad portfolio of prescription medicines for the UK largely across the vaccine, oncology and infectious disease therapeutic areas.


Role:


  • Ensures timely, accurate and compliant labelling and artwork preparation.
  • Stays updated on late pipeline filings, relevant EU and local regulations and guidelines and to develop and maintain positive relationship with key players in the regulatory environment.
  • Designs and implements regulatory adhoc local action plans, as necessary.
  • Works alongside Business Development, locally, regionally, and globally, to support business initiatives in sub region.
  • Maintains a positive relationship with internal and external regulatory contacts. GRACS on subregional, regional, and global level, MMD, EUQPPV and GCS&PV are the main contact points within the company. External contacts are regulatory authorities, aswell as other key players in the regulatory environment.
  • Ensures that marketing authorizations are maintained in compliance with related regulatory areas, through performing the necessary activities, including variations and renewals, with a high standard and within the agreed timeframes and communicates approvalsto stakeholders through the correct processes.
  • Works with Regulatory Affairs Europe to develop and implement regulatory strategies (including scientific advice and paediatric investigational plans, or orphan designation), identifies regulatory risks, and enables earliest possible approval. Ensures regulatorystrategies are aligned with local business objectives and deliverables.
  • Ensures timely preparation and maintenance of local Summary of Product Characteristics, Patient Information Leaflets, Prescribing Information, packaging material and other applicable regulatory documents according to the client and local standards and ArtworkManagement procedures.
  • Implement Prescribing Information within the correct timeframes for compliance.
  • Ensures that all internal customers receive relevant information with regard to the regulatory status of the assigned products.
  • Ensures the correct and proper utilisation of Artwork Management System to generate mockup artwork and to implement revisions to artwork.
  • Ensures efficient and consistent implementation and use of internal and external regulatory databases and systems in the country.
  • Ensures that files and archives related to Regulatory are kept updated and complete.
  • Participates in establishing and maintaining of relevant Standard Operating Procedures to secure that the current regulations are complied with.
  • Participates in implementation of updated regulatory documentation according to Agency requirements and inhouse guidance.
  • Ensures high quality translations and QRD check of Summary of Product Characteristics and Patient Information Leaflets.
  • Ensures availability of packaging material, including patient information leaflets and all other artwork in a timely and correct manner and according to relevant Artwork Management procedures.
  • Ensures adequate support to other functions to enable compliance in areas related to regulatory, such as PSUR submissions and review of promotional material.
  • Provides regulatory guidance and support to the license companies/joint venture/comarketing partners as appropriate.
  • Secures timely and adequate information and decision making with regard to regulatory issues that need to be brought to the attention of the Management Team, such as deletions, divestitures and acquisitions.
  • Takes part in subsidiary product and launch teams to provide regulatory input and strategy advice.
  • Participates, provides active input and lead if the case the local Medical Governance

Requirements:


  • Comprehension of the fastevolving EU/UK regulatory procedures especially in light of BREXIT, and EU and UK Medicines Legislation. Exposure to regulatory submissions and working with a Regulatory Authority.
  • Ability to communicate well verbally and in writing is essential, as are good organizational and planning skills.
  • Ability to identify compliance risks and escalate when necessary
  • Sound knowledge of labelling requirements.
  • Experience in managing regulatory projects
  • Meticulous attention to detail and be flexible enough to successfully handle conflicting time pressures and a large volume of work.
  • A mature and disciplined approach to work is essential as is the ability to coordinate the work of others.
  • Demonstrate diplomacy and assertive skills in dealing with internal and external parties.
Please click the link below to apply, or alternatively send an up to date CV to
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