Almac Group

Almac Group

Almac is a financially secure, privately owned organisation with over 3,700 employees located within the US, UK and Asia. 600+ companies worldwide, including all the market leaders, use our services, testament itself to the quality, innovation and efficiency of our business as proven over the past 40+ years

Our vast range of services include:

  • Biomarker Discovery & Development: Pre-clinical biomarker discovery, through to full companion diagnostic development and clinical test delivery from our CLIA lab.

  • API Services & Chemical Development: Services for all stages of drug development for small molecules, potent and cytotoxic compounds and peptides.

  • Pharmaceutical Development: Developing clinical candidates into an optimum formulation and manufacturing drug product for all phases of clinical trial supply.

  • Analytical Services: Delivering comprehensive solutions supporting drug substance and product development programmes.

  • Clinical Trial Supply: Comprehensive global clinical supply chain solutions providing physical resources and supportive technologies ensuring your clinical supply chain continually delivers across the globe. Clinical Technologies: Providing randomisation and trial supply management technology, electronic Clinical Outcome Assessments (eCOA), patient alerts and reminders, data integration and biostatistical consulting services.

Commercial Services: Providing commercial manufacturing and packaging solutions and supporting commercial product launch

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Almac Group Jobs

Manufacturing Opportunities

  • Not disclosed
  • Updated 19/02/2018
  • Armagh

The manufacturing team within Almac Sciences is currently 56 strong and a number of new positions for Manufacturing Technicians, Senior Technicians and Manufacturing Chemists are now available due to internal promotions and strengthening customer demand.

Drug Safety Specialist

  • Not disclosed
  • Updated 14/02/2018
  • Armagh

Working as part of the Regulatory Affairs team based in our global headquarters in Craigavon, you will be responsible for the day-to-day management of specialist pharmacovigilance activities in the US



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