Medical Products Laboratory Analyst (18 months FTC)

JR United Kingdom; Warrington; On-site; GBP 25,000 - 35,000; Full time

Job summary

A leading company seeks a Medical Products Laboratory Analyst for an 18-month fixed-term contract in Warrington, Cheshire. The role involves ensuring product quality and compliance with cGMP standards through quality control analysis. Candidates should have a degree in Chemistry and experience in a QC laboratory.

Qualifications

• Experience in a QC laboratory, preferably adhering to cGMP.
• Full clean driving license.

Responsibilities

• Analyze, validate, and record results to ensure quality and process control.
• Investigate abnormal results and report findings appropriately.
• Maintain laboratory equipment in compliance with cGMP.

Skills

Understanding of QC processes

Experience working according to cGMP standards

Education

Degree in Chemistry or related field

Job description

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Medical Products Laboratory Analyst (18 months FTC), Warrington, Cheshire

Client: Koura

Location: Warrington, Cheshire

Job Category: Other

EU work permit required: Yes

Job Views: 9

Posted: 06.06.2025

Expiry Date: 21.07.2025

Job Description:

This role involves providing quality control analysis services for Medical Products manufacturing, packing operations, and customers, ensuring process control, product quality, and compliance with cGMP standards. The position is initially day-shift during training, with potential shift work including nights, following a 7am-7pm pattern, 4 days on/8 days off. This is a fixed-term contract for 18 months.

Main Responsibilities:

• Analyze, validate, and record results for samples to ensure quality and process control within specifications.
• Review and validate analyses performed by other analysts.
• Prioritize tasks to meet production, sales, and customer support goals.
• Investigate abnormal results and report findings appropriately.
• Maintain laboratory equipment and processes in compliance with cGMP and SHE standards.

Qualifications:

• Degree in Chemistry or related field (desirable).

Knowledge/Experience Required:

• Experience working according to cGMP standards.
• Understanding of QC processes in the pharmaceutical industry.
• Experience in a QC laboratory, preferably adhering to cGMP.
• Full clean driving license.

Behaviors for Success:

• Develop yourself & others
• Drive results
• Provide vision & direction

We value purpose-driven individuals committed to making a difference and fostering a diverse, inclusive, and equitable workplace.