Quality Lab Analyst

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

Job summary

Join a leading global healthcare company as a QC Lab Analyst on a 12-month contract in Montrose, Scotland. This role involves performing routine analysis using classical and chromatographic techniques, ensuring compliance with Good Laboratory Practice in a regulated environment. You will work collaboratively to optimize efficiency and assist in troubleshooting production issues. This is an exciting opportunity to contribute to a company that invests significantly in research and development, offering a dynamic work environment and the chance to enhance your skills in quality control.

Qualifications

• Experience in a Quality Control laboratory setting.
• Proficiency in analytical techniques such as chromatography.

Responsibilities

• Carry out routine analysis on IPC, raw materials, and stability samples.
• Participate in activities essential for the effective operation of the quality laboratory.

Skills

Analytical Techniques

Chromatography

Quality Control

GMP Compliance

Education

Degree in Life Sciences

Tools

M-ERP

Job description

CK Group is recruiting for a QC Lab Analyst

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)

Quality Lab Analyst Role:

• Carry out routine analysis on IPC, raw materials, manufactured, and stability samples using classical and chromatographic techniques. Utilize 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 collaborative approach to optimize efficiency and reduce waste.
• Participate in activities essential for the effective operation of the quality laboratory, including reviewing and preparing procedures, validation reviews, COSHH and risk assessments, and GPS improvement activities.
• Adhere to current Good Laboratory Practice (cGLP) in a regulated environment, following established procedures.

Your Background:

• Experience in a Quality Control laboratory setting.
• Proficiency in analytical techniques such as chromatography and classical tests.
• Experience with quality and compliance in 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 UK R&D.

Location:

Montrose, Scotland

Apply:

Contact the Key Accounts Team at 01438 870011 or email [e-mail]. Please quote reference 131 951. Ensure you have the right to work in the UK.

Note: A satisfactory DBS check may be required.