Method Development&Validation Specialist– Analytical Development (Pharmaceutical Services) Location: Cork, Ireland | Full-Time | On-Site with Client Are you an experienced analytical scientist ready to take the next step in your career? We are seeking a Method Development&Validation Specialist to join a dynamic Professional Scientific Services (PSS) team supporting a leading pharmaceutical client in Cork. This is a fantastic opportunity to work in a collaborative, GMP-regulated environment where innovation, quality, and scientific excellence are at the forefront. Key Responsibilities• Lead and support method development, validation, and transfer activities in line with regulatory guidelines. • Provide technical expertise for the introduction of new products, including troubleshooting analytical challenges. • Interpret and document analytical data, ensuring compliance withALCOA+ and GMP standards. • Act as a subject matter expert in analytical techniques such as HPLC, GC, IR, LC-MS, and ICP-OES. • Mentor and train junior analysts, review technical documentation, and contribute to continuous improvement initiatives. • Communicate effectively with client stakeholders, ensuring project timelines and quality metrics are met. About You • Degree in Chemistry or a related scientific discipline. • Minimum 5 years’ experience in an analytical laboratory, ideally within a GMP environment. • Strong background in method development and validation for APIs,raw materials, and excipients. • Proficient in troubleshooting analytical instrumentation and methodologies. • Excellent communication, documentation, and problem-solving skills. • Passionate about quality, customer service, and continuous improvement. Why Join Us? • Be part of a high-performing team embedded within a global pharmaceutical leader. • Gain exposure to cutting-edge analytical technologies and diverse product portfolios. • Enjoy a supportive environment that values professional development and scientific