Almac Sciences works with organisations large and small across the globe, including the top pharmaceutical companies, Biotechs, Virtuals, and Universities. Services extend from contract R&D, through small scale custom synthesis, to cGMP synthesis up to 10s Kgs and at the levels of containment required for highly potent/cytotoxic compounds. In addition to providing support for synthesis operations, our extensive analytical facilities and expertise are available as a stand-alone service.
Almac Clinical Services
Fact: 18 out of the top 20 pharmaceutical companies trust Almac Clinical Services with their clinical supplies.
Almac Clinical Services also works with many smaller companies including biotech, virtual, CRO's and also participates in government sponsored studies. Services extend from phase one to four and include child resistant supplies for the US market and release of product by a Qualified Person on first entry into Europe.
Almac Clinical Technologies
Almac Clinical Technologies specializes in the implementation of i-nteractive trial management solutions. Almac Clinical Technologies serves both pharmaceutical and biotechnology industries, managing multiple facets of clinical trials. Almac Clinical Technologies clinical technology enables clients to expedite clinical trial development on a global scale through advanced randomization schemes, real-time enrollment data, and efficient clinical trial material (CTM) management.
Almac Pharma Services
Almac Pharma Services is an FDA-approved outsourcing partner to the international pharmaceutical and biotechnology sectors.
Almac Pharma Services offers the complete solution to your drug development needs, from formulation development, including a full range of analytical services, to commercial-scale manufacture and packaging.
With more than 25 years’ experience in the pharmaceutical industry, and with the most up-to-date technologies, we can guarantee that your product will reach your target market on time.
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The Procurement department is responsible for acquiring the desired goods using best market knowledge, at the best possible total cost of ownership, in the right quantity, of the right quality, at the right time.
Working as part of the Manufacturing team based in our global headquarters in Craigavon, you will be responsible for controlling the process operation (staff and/ or equipment) within the designated production room while assuring that the quality of the product produced complies with cGMP.
Reporting within the Project Services team, the Label Service Solutions Manager will be responsible for the management, development and commercialisation of the extended Almac Label Services offering at a global level to our client base.
Working as part of the engineering team based in our global headquarters in Craigavon, you will be responsible for assisting Project, Process and Automation Engineers with the engineering design, project management, commissioning and operation of plant and systems.
Working as part of the automation team based in our global headquarters in Craigavon, you will be responsible for assisting Project, Process and Automation Engineers with the engineering design, project management, commissioning and operation of plant and systems.
Working as part of the Manufacturing team based in our global headquarters in Craigavon, you will be responsible for carrying out operational tasks and assist with process improvement and staff development tasks while in the production areas to achieve the targets and standards set for operations.
Working as part of the Bioinformatics team, you will be responsible for providing support to Almac Diagnostics software development activities to maintain and expand bioinformatics programs/pipelines and clinical assay reporting & delivery tools.
Working as part of the Quality team based in our global headquarters in Craigavon, you will be responsible for assessing and improving the Almac Pharma Services Quality System and contribute to GMP Compliance and Quality of pharmaceutical products
Working as part of the Analytical team based in our global headquarters in Craigavon, you will be responsible for providing hands-on technical leadership of complex projects, performing all analytical activities safely and in full compliance with HSE and QA policies and procedures.
Working as part of the Quality team based in our global headquarters in Craigavon, you will be responsible for supervising and performing Quality Control functions within the Label Control/Distribution areas.
You will be responsible for electrical engineering design, project management, procurement, commissioning of electrical / automation systems and utility equipment to the highest industrial and pharmaceutical standards.
You will be responsible for liaison with Formulation Development Scientists and Analytical Support department to ensure the smooth and efficient running of Process Development activities.