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