Pharmaceutical Project Analyst

Pharmaceutical Project Analyst

Eurofins

Sandwich, United Kingdom

Job Description

• Design and guide analytical strategies to support manufacturing process development.
• Lead the planning, development, execution, and data interpretation performed by other scientists in a collaborative, matrixed environment.
• Oversee and review the development, validation, and transfer of analytical methods to ensure robust and reliable data generation.
• Manage stability studies to assess degradation pathways and establish shelf-life parameters.
• Develop impurity control strategies to ensure product quality and regulatory compliance.
• Experience with a wide range of analytical testing including dissolution, HPLC/UPLC, SFC, disintegration, compendial testing (e.g., excipients/packaging release testing), generic testing (e.g., solvents, water, ash, titrations, heavy metals, ICP/MS, UV) and compound specific methods.
• Collaborate with cross-functional teams to identify and apply the most effective analytical techniques, including the use of computational modeling, predictive tools, and data visualization platforms.
• Evaluate scientific data to draw clear conclusions, guide future work, and communicate findings through presentations, technical reports, and other media.
• Contribute to regulatory submissions by authoring relevant sections of the quality modules, ensuring alignment with global standards and expectations.
• Maintain compliance with GLP/GMP standard and safety protocols.

Qualifications

• PhD in Chemistry, or related field, with pharmaceutical R&D experience or a BSc/MSc with significant experience.
• Strong oral and written communication skills.
• Experience within a regulated laboratory environment (GLP/GMP).
• Proven ability to lead scientific projects and mentor team members.
• Proficiency in analytical instrumentation and techniques.
• Familiarity with regulatory documentation and submission processes.