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.
Working as part of the project team based in our global headquarters in Craigavon, you will manage a program of biomarker and companion diagnostic projects at Almac Diagnostics.
Working as part of the Analytical team based in our global headquarters in Craigavon, you will assist the analytical department by checking analytical data in line with company procedures and project timelines.
Working as part of the Analytical team based in our global headquarters in Craigavon, you will be responsible for the performance, monitoring and accept accountability for all assigned analytical duties relating to specific analytical projects
Working as part of the finance team based in our global headquarters in Craigavon, you will be responsible for managing and advising on the group’s taxation affairs in all countries of operation to ensure compliance with statutory requirements for both corporate and employment taxes.
The Production Supervisor is responsible for providing supervisory management support within the operational areas of Pharma Services. They will be responsible for managing a team of Operators and Senior Operators.
Working as part of the Technical Quality team based in our global headquarters in Craigavon, you will be responsible for the coordination of multiple projects on behalf of the Technical Quality Team.
The individual will be responsible for ensuring that the Temperature Services team members are trained and comply with Almac processes for delivery of the service.
Working as part of the Health & Safety team based in our global headquarters in Craigavon, you will be responsible for providing Health and Safety support to the HSE Manager within Almac Group.
The Contract Research Organisation (CRO) Operational Lead will be responsible for the success, efficiency, and continuous improvement of assigned CRO accounts at a global operational level.
The role of the Business Projects Project Coordinator is to assist Project and Program Managers on strategic projects and manage small scale projects independently, from initiation through completion with the outcome resulting in on-time/on-budget delivery according to specifications
The role of the Quality Compliance Manager is integral to the success of the Quality Department in delivering expert advice and ensuring release of clinical supplies, in line with customer expectations and regulatory demands.
the role of the Quality Compliance Team Leader is integral to the success of the Quality Department in supervising specific activities required to ensure QP Certification occurs in line with customer expectations and regulatory demands
The Finance Analyst will have responsibility for the timely presentation and interpretation of certain monthly analyses of sales, gross profits and margins across a range of customers’ projects and business areas for various internal stakeholders.