​Our client is a pioneering pharmaceutical company dedicated to transforming medicine through advanced drug delivery technologies. Our mission is to improve patient outcomes by developing innovative long-acting injectable therapies that provide sustained, controlled release of active pharmaceutical ingredients. Our collaborative and dynamic work environment fosters creativity, scientific excellence, and a commitment to making a real impact on global health.

Position Overview: we are seeking an experienced and highly motivated Analytical Scientist to join our client's R&D team. The successful candidate will play a critical role in the development and characterisation of our innovative drug delivery systems. This position requires a deep understanding of analytical techniques, problem-solving skills, and a passion for scientific discovery.

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Key Responsibilities:

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• Method Development:

  Design and develop robust analytical methods for the characterisation and quantification of active pharmaceutical ingredients (APIs) and excipients in various formulations.

• Validation:

  Conduct method validation in accordance with regulatory guidelines (ICH, FDA, EMA) to ensure accuracy, precision, specificity, linearity, and robustness.

• Sample Analysis:

  Perform routine and non-routine sample analysis using advanced analytical techniques such as Particle Size Determination, DSC, HPLC, UPLC, GC, LC-MS, NMR, FTIR, and UV-Vis spectroscopy.

• Data Interpretation:

  Analyse and interpret complex data sets to provide insights into the physicochemical properties of drug formulations and their stability profiles.

• Documentation:

  Prepare detailed technical reports, method validation protocols, standard operating procedures (SOPs), and regulatory submission documents.

• Collaboration:

  Work closely with cross-functional teams, including formulation scientists, process engineers, and quality control, to support the development and optimisation of drug delivery systems.

• Troubleshooting:

  Identify and troubleshoot analytical challenges, providing innovative solutions to support project timelines and objectives.

• Compliance:

  Ensure all laboratory activities comply with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).

Qualifications:

• Education:

  Ph.D. in Analytical Chemistry, Pharmaceutical Sciences, or a related field. Candidates with a Master’s degree and 4years relevant experience will also be considered.

• Experience:

  Minimum of 3-5 years of hands-on experience in an analytical laboratory within the pharmaceutical or biotechnology industry.

• Technical Skills:

  Proficiency in chromatographic techniques (HPLC, UPLC, GC), Particle Size Determination or DSC or Rheology and spectroscopy methods (LC-MS, NMR, FTIR, UV-Vis). Experience with method development and validation is essential. Knowledge of QbD principals and KF/FT-IR would be a bonus.

• Regulatory Knowledge:

  Familiarity with regulatory requirements and ICH guidelines for analytical method validation and pharmaceutical development.

• Software:

  Experience with analytical software and tools such as Empower 3, Morphologi G3, ChemStation, or equivalent.

• Soft Skills:

  Strong analytical thinking, attention to detail, excellent written and verbal communication skills, and the ability to work effectively in a team-oriented environment.

• Problem-Solving:

  Demonstrated ability to troubleshoot complex analytical issues and develop practical solutions.