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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Almac are seeking synthetic chemists to join our process development group, whose main aim is to develop chemical processes to allow successful manufacture of drug substance to support toxicology, clinical trials and commercial supply.
We have several opportunities at a range of levels in our Analytical Development Group, Quality Control and Analytical Services. We prefer candidates with experience of working in a GMP pharmaceutical analysis laboratory, with previous experience using HPLC and GC analytical methods.
Working as part of the Logistics team based in our global headquarters in Craigavon, you will be responsible for providing support for the Logistics Department and will be responsible for the effective co-ordination of activities associated with ensuring Customs compliance.
Working as part of the Analytical team based in our global headquarters in Craigavon, you will be responsible for analytical activities associated with drug substances and/or drug products. This may involve method development & validation, release testing and stability testing.
Working as part of the Finance team based in our global headquarters in Craigavon, you will be responsible for To ensure the timely posting, updating and paying of supplier invoices and the preparation of monthly purchase ledger reports.
The role involves working within the Technical Quality team to ensure compliance with the principles of GMP and Almac’s quality standards. This team will be responsible for a range of activities although the primary focus will be Process and Packaging Validation.