We are seeking a motivated, hands-on individual who is eager to develop their skills further in formulation and process development. In this role, you will work closely with the R&D Manager and wider team to support formulation development, scale-up activities, and technical transfers. You will gain valuable experience working with production-scale machinery, conducting formulation trials, and supporting the successful transfer of products into commercial manufacture. In this role you will report to the Veterinary R&D manager.Location:5 days onsite in R&D Lab, LoughreaAs an Associate R&D Formulator (Veterinary) your key responsibilities will be as follows:Assist with formulation development and scale-up of solid, semi-solid, and liquid dosage forms under the guidance of senior team members.Operate and support the setup of production-scale equipment for R&D and pilot-scale activities.Conduct and accurately document formulation trials in compliance with GMP and internal procedures.Support technology transfer activities, including process optimisation, pilot batches, and troubleshooting as required.Help prepare batch records, protocols, and reports, ensuring accuracy and compliance with quality standards.Coordinate with production, planning, validation, procurement, and engineering teams to support project timelines.Follow all health, safety, and GMP requirements, contributing to a safe and compliant working environment.Assist with investigations, deviations, and change controls in collaboration with QA and R&D leadership.Maintain good housekeeping and equipment care in laboratory and pilot areas.Review the draft process validation filled protocols and reports and ensure that all the data is correct and the reports are issued on time.Perform the Lab development trials for successful development of formulation where required.Execution of manufacturing of optimization and pilot batches where required.Review and approval of all pilot batch documentation including Work Orders and Process Validation Protocols.Participating in internal/external audits of the R&D function.Ensuring that existing R&D and Quality procedures are followed in all areas and where appropriate suggestions/change control forms prepared such that the quality system can be improvedTo liaise with QA for raising change controls, deviations, investigations, CAPA in the Q-pulse and reference to Quality Management SystemEducation & Experience:Ideally educated to degree level in pharmaceutical sciences, chemistry, chemical engineering, or a related field, or has equivalent practical experience working within pharmaceutical or manufacturing processes.Experience of working in a GMP manufacturing/laboratory environment is desired along with a clear understanding of (GMP) principles.Familiarity with oral solid or liquid dosage manufacturing processes would be an advantage.Skills and Competencies:Strong practical and mechanical aptitude; comfortable working with manufacturing equipment.Excellent attention to detail and methodical approach to documentation.Collaborative team player with good communication skills and willingness to learn.Proactive approach to problem-solving and supporting continuous improvement.Ability to manage multiple tasks in a fast-paced environment.Displays flexibility, willingness to succeed and goes the extra mile.Good computer literacy, including MS Office (Word, Excel)Applicants from diverse backgrounds, including those returning after a career break or with transferable skills from non-traditional career paths, are encouraged to apply. We value varied experiences and are committed to fostering an inclusive environment that supports individuals with disabilities. This position is only open to candidates who already hold valid work authorisation for the EU.