Quality Lab Analyst

TN United Kingdom; Montrose; On-site; GBP 80,000 - 100,000; Full time

Job summary

Join a leading global healthcare company as a QC Lab Analyst in Montrose, Scotland. This role offers an exciting opportunity to engage in routine and non-routine analysis, utilizing classical and chromatographic techniques. You'll be part of a dynamic team dedicated to optimizing laboratory operations while adhering to Good Laboratory Practices in a highly regulated environment. If you have a passion for quality control and a commitment to excellence, this position is perfect for you. Contribute to innovative healthcare solutions and be part of a company that invests significantly in research and development.

Qualifications

• Experience in a Quality Control laboratory is essential.
• Competency in chromatographic techniques and classical tests.

Responsibilities

• Conduct routine analysis on IPC, raw materials, and stability samples.
• Provide analytical services for non-routine samples and troubleshoot production issues.

Skills

Chromatography

Analytical Techniques

Data Management

Collaboration

Quality Control

Education

Degree in Chemistry or related field

Tools

M-ERP

Job description

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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.

Pay rate: £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, 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 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 highly regulated environment, following established procedures such as LSOPs and GSOPs.
• Previous experience in a Quality Control laboratory.
• Competency in analytical techniques such as chromatography and classical tests.
• Experience working in a GMP-compliant quality or compliance environment.

Company:

Our client is a leading global healthcare company engaged in researching, developing, and supplying innovative medicines, vaccines, and healthcare products, with headquarters in the UK. They invest approximately £1 billion annually in UK research and development.

Location:

The role is based at the client's site in Montrose, Scotland.