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Contact Info
Paula O'Reilly
Life Science

+353 1 507 9265
[email protected]
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Details

Trade Compliance Manager


Reference:POR/634475 Location: Limerick
Qualification:DegreeExperience:7-9 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: Compliance Specialist

A Trade Compliance Manager is required to join a leading biotechnology company in Limerick. The Associate Manager/Manager Trade Compliance will be responsible for the direction, organisation and supervision of all Trade Compliance activities within a pharmaceutical industry operation.

The Role

  • Responsible for delivery of all Trade Compliance requirements for the site.
  • Maintains a strong working relationship with external bodies (e.g. Customs, Revenue, Department of Agriculture) and works to resolve items as they arise through cross- functional team engagement.
  • Leads the Revenue Customs relationship and maintains up to date records for all Revenue and Customs requirements.
  • Ensures all requirements are in place to meet obligations as an AEO (Authorised Economic Operator).
  • Lead all Revenue Authorisation’s including the Customs Warehouse and Inward Processing, EIDR and Comprehensive Guarantee.
  • Ensure the Trade Compliance process/Systems are robust.
  • Follows established safety practices and SOPs in a cGMP environment.
  • · Provides coaching to your team, including employee development plans, and champions a healthy work environment where employees feel valued and respected.

    The Person
  • As Associate Manager you must hold a Bachelor’s degree in Business, Supply Chain Management or Science background and 6 years of relevant experience.
  • As Manager, you must hold a Bachelor’s degree in Business, Supply Chain Management or Science background and 7 years of relevant experience or equivalent combination of education and experience.
  • Also, experience in a related industry within a Trade Compliance role is preferred and if you have experience with Inward Processing, Authorised Economic Operator and Known Consignor that is a plus. GMP regulated and pharmaceutical/biotech experience is an added advantage.

    This role might be for you if:
    • You have previous experience in planning, drug development, performance metrics and project management.
    • You have the ability to lead multiple, complex projects and changing priorities and work effectively in a team environment.
    • You have a strong working knowledge of supply chain management at both the development stage for clinical supplies as well as at the commercial stage a plus.
For further details please contact; Paula O’Reilly on 087 7094141 or send CV in confidence to [email protected]