We are looking for an individual who will support and drive Chanelle Pharma's vision to be the most valued global provider of high quality, competitively priced pharmaceutical products and to provide excellent services and support to our customers. This is a key role in the research and development team reporting to the Head of R&D Veterinary, ensuring high standards of R&D product development to ensure R&D pipeline deliverables are met according to the company's strategic plan. In this role you will report to the Vet R & D manager.Location: Based onsite at our R&D Laboratory in either Loughrea Ireland or Amman, JordanAs an R&D Formulator (Veterinary) your key responsibilities will be as follows:Perform formulation development and scale-up of solid, semi-solid and liquid dosage formulations and process development for US/Europe/Canada/US/Australia and global markets.Provide Technical support in evaluation of new molecules which involves checking the feasibility of development and manufacturing within the in-house infra structure.Complying with all the relevant regulatory guidelines for European and US FDA, ICH guidelines for development, process validation, scale-up and stability studies.Familiarity with operation principles of standard manufacturing equipment used in solid and semi-solid oral dosage forms and liquid dosage forms and GMP principals required for scale up batches (including biostudy batches)Provide Technical support to Registration for responding to the queries from the regulatory agencies.Prepare development reports ensure submission of required information to Registration in a timely manner with correct data.Prepare batch manufacturing, packaging records and R&D process validation protocols and reports stability protocols and reports and familiarity with Bill of Material.Assist in the transfer of R&D Vet products into production for API/site variation and or Jordan Products.Ensure the log books/experiment registers are completed according to requirements.Co-ordinate with planning/production/validation/Jordan teams where relevant to ensure timely completion of project targets.Co-ordinate with procurement/Engineering to ensure availability of required documentation and suitability of packaging materials on the exiting lines.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 SysteEducation & Experience:Graduate or Post graduate qualifications in pharmaceutical sciences is essential.At least 6 years formulation development or process development experience in the pharmaceutical industry.Experience in the formulation of oral solid & liquid dosage forms.Experience working within a pharmaceutical cGMP Environment; with knowledge of EU GMP and US FDA GuidelinesSkills & Competencies:Excellent analytical, reasoning and science skillsStrong analytical science backgroundEstablishes strong working relationships with others, building team rapport and creating a cohesive team environment.Displays a positive outlook with strong coaching skills, maintaining interest at all times.Methodical, systematic and structured approach to organising work. Practical, action-orientated approach to managing priorities.Makes effective and consistent decisions in a timely manner.Positive and proactive person who is energised by having great responsibilityTakes personal responsibility for making a decision and taking action within their own area.Escalates issues appropriately.Takes action to correct poor performance by being fair and consistent in approach.Displays flexibility, willingness to succeed and goes the extra mile.Strong computer skills in MS Office, Excel and other relevant analytical software.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.