R&D Analyst

Job DescriptionR&D Analyst ABOUT XEOLAS Xeolas is an Irish-owned speciality Pharmaceutical company located in Dublin, Ireland with 80+ employees. We develop and manufactureinnovativepatient friendly pharmauceutical products for international markets. We are now seeking an experiencedR&D Analystas weexpand.

OVERALL ROLE OBJECTIVE The experiencedR&D Analystwill report directly to the R&D Manager/Supervisor and be closely involved in all aspects of Development and Validation activities as well as liaising with Quality Control and R&D fucntions within the company. SPECIFIC RESPONSIBILITIES Responsible for analytical method R&D and also validation for new and existing products Responsible for coordinating new product introductions and method transfers into the laboratory. To prepare, review and approve method development, method validation and equipment protocols, as required.

To conduct and report test method development, validation and technical transfer ensuring that scheduled work is completed accurately and within agreed timelines. To assist in trouble-shooting issues with existing methods and within the QC laboratory. To provide data for regulatory submissions.

To write and review relevant sections of regulatory submissions. To liaise with other departments in relation to testing requirements, as necessary. To ensure that all work is conducted, and all relevant documentation is maintained, to an acceptable GLP standard.

To ensure effective and timely closure on all technical issues, OOS, OOT and Deviation Investigations/Reports, as applicable. To prepare, review and approve SOPs, as required. To provide technical support and problem solving for equipment and other methods, including pharmacopoeia, as required.

To ensure that work is carried out safely and in line with the company Health and Safety statement and relevant SOPs. To bring to the notice of management any discrepancies, deviations or non-conformances in testing or work practice. To ensure good housekeeping practices within the laboratory.

Staff mentoring. Staff training. Trending of data, as required.

KEY SKILLS / EXPERIENCE REQUIREMENTS Degree in Pharmacy or Chemistry or similar qualification. At least 1 years relevant analytical method development / method validation experience in a pharmaceutical laboratory. cGMP / GLP / GDP will be added advantage. Highly flexible, works well in a team environment, and has necessary skills to organize, mobilize, communicate, influence and lead.

Excellent critical thinking and problem-solving abilities. Excellent Project Management Skills Strong interpersonal and communication skills Empower 3 LC Software Experience desirable but not essential Kindly send your CV at harish.bhat and on or before 11th Sep 2026. TPBN1_IJ