We are partnering with a leading pharmaceutical manufacturer based in Dublin 15 to source an Analytical Scientist for a 12-month contract opportunity. This role offers competitive hourly rates and the chance to work within a dynamic Global Operations & Quality team, providing critical analytical support on laboratory projects, technical investigations, and material assessments at a state-of-the-art manufacturing facility.
Reporting to the Senior Manager, Technical Operations, you will perform and oversee analytical laboratory activities with a strong hands-on analytical focus. The role includes RP-HPLC, size-exclusion chromatography, and LC-MS analysis of peptide-based products, biologically derived polymers, and other complex molecules. You will develop, optimise, troubleshoot, and execute analytical methods while providing scientifically sound assessments of analytical results.
Key Responsibilities
- Perform hands-on RP-HPLC analysis of peptides, peptide-based products, and other biological or large molecules, including method development, optimisation, qualification, validation, transfer, and routine execution.
- Develop and execute size-exclusion chromatography (SEC/GPC) methods for synthetic polymers, biologically derived polymers, and other complex macromolecules.
- Operate LC-MS systems and perform sample analysis, data processing, spectral interpretation, and advanced mass analysis, including accurate-mass determination, spectral deconvolution, peptide mapping, and MS/MS interpretation.
- Perform first-line troubleshooting of HPLC, UPLC, and LC-MS instrumentation, including pumps, autosamplers, detectors, pressure problems, leaks, chromatography performance, and software-related issues.
- Review, interpret, and trend analytical data, providing scientifically justified assessments of analytical results and supporting investigations of atypical, out-of-trend, and out-of-specification results.
- Draft, review, and maintain SOPs, analytical methods, protocols, technical assessments, laboratory investigation reports, method-development reports, and validation or qualification reports while ensuring compliance with GMP, data-integrity, and laboratory documentation requirements.
Requirements
- PhD, MSc, or BSc in Chemistry, Biology, Engineering, or a related science; strong analytical background required.
- Minimum 3-5 years of hands-on analytical laboratory experience in a pharmaceutical, biopharmaceutical, or other regulated GMP environment.
- Demonstrated hands-on experience with RP-HPLC analysis and method development for peptides, peptide-based products, proteins, or other biological molecules.
- Practical experience operating LC-MS instrumentation and interpreting complex mass-spectrometry data, including experience with SEC/GPC methods for synthetic or biologically derived polymers.
- Proven ability to troubleshoot chromatography methods and perform first-line diagnosis and maintenance of HPLC, UPLC, or LC-MS equipment, with experience in analytical method development, optimisation, qualification, validation, method transfer, and lifecycle management.
- Strong working knowledge of GMP, laboratory data integrity, and good documentation practices, with excellent communication skills and the ability to work effectively in a cross-functional team environment.