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Početni (0-2 godine), Srednji (2-5 godina), Senior (5-10 godina)

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A fantastic opportunity for a Tech Services Specialist to going a global pharma company based in Kildare, Ireland


The site is an integral part of the global solid oral dose network; manufacturing tablets and capsules for world markets using highly complex processes. This site has been an established leader in the supply of medicines for over twenty years and is currently expanding its portfolio. The Technical Services team is recruiting for colleagues to work with us at this exciting time for the facility.

We support the commercial supply and technical transfer of products using a range of technologies such as Process Analytical Technologies and Advanced Process Control. We continuously improve and enhance our facility through the execution of complex projects introducing next generation manufacturing processes. These are deployed using six sigma and lean methodologies.

We have a pilot scale plant (the Technology and Innovation Centre) with the capability of carrying out development at 1kg to 50kg scale across all principle unit operations. We own the validation of the manufacturing and cleaning processes which supply all markets including the USA, EU and Asia. We work in a fast paced environment where learning and personal development are actively encouraged.

We pride ourselves on our culture of high performance team work and innovation which enables the business to deliver on its commitments.



The role of Technical Services Specialist will include the following responsibilities:

  • Preparation and execution of protocols and reports. This includes development and validation (process and cleaning).
  • Building expertise of products and processes that he/she supports including trending and interpretation of data.
  • Execution of continuous improvement projects (six sigma methodology experience would be an advantage).
  • Investigating and troubleshooting all routine technical problems during normal activities. Support to commercial manufacturing team and technical transfer projects.
  • He/she will adopt a risk-based approach to problem solving, determination of root cause, issue resolution and recommendation.
  • They will be aware of new methodologies pertinent to his/her function and is able to introduce them with limited supervisory input. Is accomplished with all fundamental technologies.
  • Preparation and updating of appropriate GMP documentation, forms, protocols and procedures.


Qualification Requirements:

Educated to degree level in Science, Pharmacy or a related discipline

Experience in the Pharmaceutical industry, preferably in solid oral dose manufacture.


If you are interested in contributing within a world leading company,  in the manufacture of medicines which improves the lives of patients join the Newbridge Technical Services Team.