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Job : Analyst Location : North West A rapidly growing Biotech specializing in bioanalysis pivotal to advancing drug discovery and regulatory development programs. As an Analyst you'll play a vital part in method development, validation, and routine sample analysis while ensuring strict compliance with GLP/GCP standards. Analyst Key Responsibilities: Assist in bioanalytical projects by contributing to method development, validation, and sample analysis. Conduct LC-MS/MS and/or Ligand Binding Assays, with responsibilities including troubleshooting and instrument upkeep. Participate in data analysis and support report preparation. Collaborate closely with Project Managers to meet project deadlines. Perform sample extractions. Maintain awareness of and adhere to regulatory guidelines. Minimal Requirements: Strong communication skills and ability to collaborate effectively. Results-driven with a strong commitment to quality work. Bachelor's degree in life sciences or related field. Ideal Requirements: Exposure to working in a regulated setting. Proficiency in Microsoft Office suite. Hands-on experience with LC-MS/MS and Ligand Binding assays is advantageous. Familiarity with scientific software platforms. Ability to thrive in a collaborative team setting. Benefits: £25,000 based upon experience. Generous holiday allowance: 28 days, including public holidays. Company pension scheme. Flexible working hours to support work-life balance. Note : We regret to inform you that sponsorship is unavailable for this position. Application : If you meet the qualifications for this role, we encourage you to apply, and we will contact you promptly.