Quality Control Analyst

SRG; Skipton; On-site; GBP 26,000 - 32,000; Full time

Job summary

SRG is seeking a QC Analyst (Temporary) for an on-site role in Skipton, UK. This temporary 3-month position will support a GMP manufacturing site in North Yorkshire and may be extended.

The successful candidate will perform analytical testing on raw materials, intermediates, packaging materials and medicinal products within a GMP laboratory, with an urgent start as soon as the 1st of September. Key responsibilities include conducting HPLC, UV-VIS, titration, Karl Fischer and TOC analyses,

Qualifications

• Degree in Chemistry or related scientific field.
• Experience with HPLC, UV-VIS and physicochemical tests.
• Experience working in a GMP environment.
• Available for immediate start.

Responsibilities

• Perform analytical and physical tests including HPLC, UV-VIS, DLC, MID-IR, titration, Karl Fischer, TOC.
• Release of raw materials, semi-finished products and packaging materials for use in production.
• Perform analysis for process, product, cleaning and equipment validation studies.
• Conduct analysis for stability studies and method transfers.
• Maintain stringent GMP quality standards in the laboratory.

Skills

GMP experience

Education

Degree in Chemistry

Tools

HPLC

UV-VIS

Auto-Titrators

Karl Fischer

TOC

Job description

QC Analyst (Temporary)

Skipton, UK (On-site)

Temporary 3 Month

SRG are recruiting for a number of QC Analysts to support a busy GMP Manufacturing site in North Yorkshire. This will be a temporary position for an initial period of 3 Month with the potential to be extended.

This is an urgent position and can start as soon as 1st of September.

As part of the QC team, you will play a crucial part in carrying out Quality testing on raw materials, semi-finished goods, packaging materials, and medicinal products, all within a GMP environment.

Key Responsibilities

• Performing analytical and physical tests including HPLC, UV-VIS, DLC, MID-IR, (auto) titration, water determination Karl Fischer, TOC, etc.
• Releasing of raw materials, semi-finished products and packaging materials for use in production
• Performing analysis for process, product, cleaning and equipment validation studies
• Conducting analysis for stability studies & method transfers to or from other laboratories.
• Ensuring stringent GMP Quality standards are maintained throughout the laboratory.

Required

• A degree or similar experience in Chemistry or a relevant scientific field.
• Experience in using HPLC, UV-VIS, Auto-Titrators and physicochemical tests.
• Experience of working in a GMP environment.
• Available for an immediate start.