GMP Analytical Scientist – Formulation & Method Transfer

Quotient Sciences

Nottingham

Hybrid

GBP 34,000 - 48,000

Full time

2 days ago
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Job summary

Quotient Sciences is a leading drug development and manufacturing accelerator, seeking an Analytical Scientist for a 12 month contract in Nottingham, UK. You will perform analytical testing to support formulation development and method transfer within a GMP/GxP framework.

You will work with HPLC, UV spectroscopy and dissolution testing, contributing to QA and documentation, and supporting a collaborative scientific team to meet project timelines and quality standards.

Qualifications

  • Requires HNC/HND in Chemistry or closely related discipline.
  • Experience in a Quality Control or analytical laboratory.
  • Experience with HPLC, UV spectroscopy and dissolution testing.
  • Strong documentation and GMP understanding.

Responsibilities

  • Perform analytical testing to support formulation development and process transfer.
  • Conduct sample analysis using HPLC, UV spectroscopy and dissolution testing.
  • Prepare and review GMP-compliant laboratory documentation.
  • Write and update SOPs and analytical methods.
  • Support training and development of team members.
  • Ensure compliance with GMP, GxP and QA standards.
  • Maintain safety and housekeeping standards.
  • Collaborate across the lab to meet project deadlines.

Skills

HPLC
UV spectroscopy
Dissolution testing
Documentation
GMP/GxP awareness
Teamwork
Communication
Problem solving
Laboratory safety
Quality systems

Education

HNC/HND in Chemistry or closely related scientific discipline

Tools

HPLC
UV spectroscopy
Dissolution testing

Job description

Quotient Sciences is a leading drug development and manufacturing accelerator, seeking an Analytical Scientist for a 12 month contract in Nottingham, UK. You will perform analytical testing to support formulation development and method transfer within a GMP/GxP framework.

You will work with HPLC, UV spectroscopy and dissolution testing, contributing to QA and documentation, and supporting a collaborative scientific team to meet project timelines and quality standards.

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