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.
you will oversee analytical training within Analytical Services, Analytical Development, Physical Sciences and Quality Control: to include basic analytical techniques and GMP procedures.
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.
We are seeking to expand our team within the Project Services Department. We are looking for individuals with strong project management skills who can bring their knowledge and expertise to our industry – full industry training will be provided.
you will be responsible for assisting with development and delivery of instrument based analytical training for the Analytical Departments (QC, AS, AD, PS) within the Quality Unit
you will be responsible for supporting the daily, efficient running of the device design control and risk management activities in Almac Diagnostics Laboratories
We are looking for individuals from a chemistry or manufacturing background who can bring their knowledge and expertise to our teams – full appropriate training will be provided.
The Key Account Manager (KAM) is part of the Clinical Services Business Development team and is responsible for the business relationship and management of all assigned key accounts.
you will coordinate and manage activities in support of process transfer and GMP manufacturing.
The Procurement Specialist is responsible for all aspects of Procurement within a defined supply category and will support other supply categories as necessary.
your main role is to be the process scale up expert for your shift to aid the transfer of chemical processes from the laboratory into the GMP Manufacturing Plant
you will be responsible for performing molecular biological analyses as required and to assist in the daily, efficient running of the Almac Diagnostics Laboratories.
The post holder will be responsible for providing administrative support to the Group Facilities Department (Craigavon).
Responsible for the delivery of planned internal communication and PR activities.
The post holder will conduct chemical testing following set procedures, maintain accurate records of work and conduct all analysis following GMP and/or internal procedures.