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Development technologist

  • Salary: Negotiable
  • Job type: Permanent
  • Location: Waterford
  • Sector: Science
  • Date posted: 31/07/2017
  • Job reference: J371410A
This vacancy has now expired.

Job description

Responsible for the Formulation Development of Generic and New Drug Products through:

  • Applying a thorough knowledge of all processes involved in the manufacture of pharmaceutical products.
  • Applying a thorough knowledge of pharmaceutics to the development of drug products and the interpretation of in-vitro data to predict in-vivo performance.
  • Performing formulation, process development and optimization trials using experimental design techniques
  • To carry out pre-formulation and formulation development trials on high potency molecules.
  • Manufacture, pack and label clinical batches for human consumption.
  • Communication of project data at internal meetings and through formulation reports and presentations.
  • Lead pivotal scale cGMP exhibit batch based upon a sound knowledge of site and departmental SOPs, and an understanding of ICH/FDA/EMEA requirements as they relate to formulation and process development activities.
  • Generate GMP documentation, e.g. SOPs, Batch Manufacturing Records and protocols.
  • Maintain a comprehensive knowledge of formulations and process development disciplines through research and scientific literature.


  • To ensure that all work carried out is in compliance with the required regulatory and health and safety standards.
  • To comply with company policies and procedures.
  • To process batches of products/ components/ raw materials in an efficient and timely manner to meet with project timelines.
  • To complete all documentation in real time where applicable and within the agreed turnaround times and to ensure right first time.

To work within a team environment to ensure all project timelines are met.

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