Quality lab analyst 106110 (3)

CK Group; Montrose; On-site; GBP 80,000 - 100,000; Full time

Job summary

An established industry player is seeking a QC Lab Analyst to join their dynamic team on a 12-month contract. This role involves performing routine and non-routine analysis using classical and chromatographic techniques, ensuring compliance with Good Laboratory Practice in a highly-regulated environment. The ideal candidate will have prior experience in a Quality Control laboratory and be skilled in analytical techniques. Join a leading global healthcare company that invests significantly in research and development, contributing to innovative healthcare solutions. This is an exciting opportunity to make a meaningful impact in the pharmaceutical industry.

Qualifications

• Experience in a Quality Control laboratory is essential.
• Competency in analytical techniques such as chromatography.

Responsibilities

• Conduct routine analysis on IPC, raw materials, and stability samples.
• Participate in quality laboratory operations and documentation.

Skills

Chromatography

Classical Testing Methods

Quality Control

GMP Compliance

Tools

M-ERP

Job description

CK Group is recruiting for a QC Lab Analyst to join one of the top ten companies in the pharmaceutical industry on a 12-month contract basis.

Salary:

PAYE £20.97 per hour (inside IR35)

Role Responsibilities:

• Carry out routine analysis on IPC, raw materials, manufactured, and stability samples using classical and chromatographic techniques, including the use of M-ERP and other IT systems for data management and reporting.
• Provide analytical services for non-routine samples and assist in troubleshooting production issues.
• Perform tasks with integrity, a positive attitude, and a willingness to collaborate across boundaries to optimize efficiencies and reduce waste.
• Participate in activities essential for the effective operation of the quality laboratory, including reviewing and preparing procedures such as LSOPs, validation reviews, COSHH, risk assessments, and GPS improvement activities.
• Work in accordance with current Good Laboratory Practice (cGLP) in a highly-regulated environment, following defined procedures and documentation.

Your Background:

• Previous experience in a Quality Control laboratory.
• Competency in analytical techniques such as chromatography and classical testing methods.
• Experience in quality and compliance within a GMP environment.

Company:

Our client is a leading global healthcare company involved in researching, developing, and supplying medicines, vaccines, and healthcare products, headquartered in the UK. They invest approximately £1bn annually in R&D in the UK.

Location:

Montrose, Scotland.

Application Process:

For more information or to apply, contact the Key Accounts Team at 01438 870011 or email [e-mail]. Please quote reference 131 951.

Applicants must have the right to work in the UK. This role may require a satisfactory DBS check.