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Technical Manager

Job LocationLeicester
EducationNot Mentioned
Salary£33,000 - £38,000 per annum
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent, full-time

Job Description

Technical Manager Salary c£35k dep on experience and benefitsThe Company: Our client is a leading UK based consumer healthcare provider. They supply UK & European retailers with high quality branded and own branded eye / healthcare products. They are looking to appoint a Technical Manager working from their site near Melton Mowbray.The Role: Working within the Quality / Technical / Regulatory department. You will provide Technical support to the company’s Customers, Suppliers and Regulatory Bodies. Ensuring their products comply with relevant legislation such as GDP, ISO 13485 and BRC requirements. That they fulfil its obligation as legal manufacture of medical devices and MHA holder for licenced medicines.Key responsibilities and duties include:

  • To provide support to the Head of Compliance
  • Completion and accuracy of customers technical databases, through new product set up and on-going maintenance
  • Point of initial technical contact with customers and suppliers, including raising issues when required to Head of Compliance
  • Management of product registrations in-line with sales demand utilising external and internal support where required
  • Supporting the Pharmacovigilance system, ensuring business compliance, supporting external consultants where required
  • Management of product technical compliance through MHRA Approvals, Notified Body Approvals, etc.
  • Providing technical support to external medical device consultants
  • Ensuring technical agreement compliance across the business
  • Completion of customer and supplier technical paperwork
  • Management of UK REP activities
  • The ideal candidate will have:With a background in pharmaceutical manufacturing and a strong understanding of current GMP and technical processes you will consider yourself to be highly motivated and a natural leader.
  • At least 3 years’ experience within a regulated environment, ideally medical devices or medicinal products
  • Understanding of regulations supporting healthcare product development, ie GMP, GDP, Medical Device ISO 13485
  • Experience of operating within a Quality Management system
  • Ability to evaluate information and draw conclusions based on facts.
  • Experience in conducting internal audits
  • Key phrases: Technical Manager, QA, HACCP, Melton Mowbray Required skills
  • GDP
  • GMP
  • ISO
  • BRC
  • Keyskills :
    GDP GMP ISO BRC

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