Job Title: Method Development and Validation Specialist
About the Role
This is an exciting opportunity to join a dynamic team of analytical scientists in Cork, Ireland. As a Method Development and Validation Specialist, you will be responsible for leading and supporting method development, validation, and transfer activities in line with regulatory guidelines.
Key Responsibilities
* Develop, validate, and transfer methods for pharmaceutical products and raw materials
* Provide technical expertise for the introduction of new products and troubleshoot analytical challenges
* Interpret and document analytical data, ensuring compliance with ALCOA+ 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
About You
* Bachelor's 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
Benefits
This role offers a supportive environment that values professional development and scientific integrity. You will have the opportunity to work in a collaborative, GMP-regulated environment where innovation, quality, and scientific excellence are at the forefront.
You will gain exposure to cutting-edge analytical technologies and diverse product portfolios. This is a fantastic opportunity to take your career to the next level and make a real impact in the pharmaceutical industry.
Join our team of analytical scientists and contribute to the development of innovative pharmaceutical products. Apply now and take the first step towards a challenging and rewarding career.