GMP Analytical Chemist: HPLC/GC & Method Development

Sterling Pharma Solutions; Cramlington; Hybrid; GBP 32,000 - 42,000; Full time

Job summary

Sterling Pharma Solutions is seeking an Analytical Chemist to perform analysis and related activities for substances and materials in line with cGMP. You will maintain records, prepare samples and collaborate with stakeholders at the Cramlington site in Northumberland.

Responsibilities include method development, method validation support, calibration of lab equipment, and GMP-compliant reporting. Strong communication and flexibility are essential, with Chromeleon CDS experience preferred.

Qualifications

• Degree in Chemistry or a relevant scientific discipline.
• Experience in GMP environments is preferred.
• Strong knowledge of HPLC and GC techniques.
• Good verbal and written communication skills.
• Flexible and able to manage changing priorities.
• Experience with Chromeleon CDS is desirable.

Responsibilities

• Perform analysis and report results in accordance with cGMP requirements.
• Optimise analytical methods and support transfer of processes into production.
• Investigate deviations and OOS results, contributing to root causes.
• Calibrate and maintain analytical laboratory equipment.
• Carry out routine auditing of laboratory areas.
• Carry out SAP transactions in a timely and accurate manner.
• Support method validation and cGMP stability programs.
• Characterise reference materials for use in cGMP analysis.
• Develop and prepare analytical methods and SOPs as required.
• Liaise with manufacturing and quality personnel on compliance matters.

Skills

Analytical Chemistry

HPLC

GC

CDS (Chromatography Data System)

Documentation

Team collaboration

Education

Degree in Chemistry

Tools

Chromeleon

Job description

Sterling Pharma Solutions is seeking an Analytical Chemist to perform analysis and related activities for substances and materials in line with cGMP. You will maintain records, prepare samples and collaborate with stakeholders at the Cramlington site in Northumberland.

Responsibilities include method development, method validation support, calibration of lab equipment, and GMP-compliant reporting. Strong communication and flexibility are essential, with Chromeleon CDS experience preferred.