Medical Products Laboratory Analyst (18 months FTC)

ZipRecruiter; Runcorn; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading company in the pharmaceutical sector is seeking a Medical Products Laboratory Analyst for an 18-month fixed-term contract. The role involves quality control analysis to ensure compliance with cGMP standards, including sample evaluation, review of analytical work, and maintaining the laboratory environment. Ideal candidates will possess an HNC/HND in Chemistry and have experience in QC within the pharmaceutical industry, contributing to a diverse and inclusive workplace.

Qualifications

• Minimum qualification of HNC/HND in Chemistry required.
• Experience working to cGMP standards in a QC laboratory.
• Full clean driving license preferred.

Responsibilities

• Analyze, validate, and record results for medical products samples.
• Review analyses performed by other analysts.
• Maintain laboratory and equipment to cGMP standards.

Skills

Quality Control Analysis

cGMP Compliance

Analytical Skills

Education

HNC/HND in Chemistry

Degree in Chemistry or related field

Job description

Job Description

You are purpose-driven, growth-minded, and ready to stretch your potential. That’s the spirit of the community at Orbia, where our purpose to advance life around the world drives our global team of over 23,000 employees every day.

We create solutions to deliver clean water, secure food supplies, and reliable information. We also lead advances in green and smart cities, transportation, and healthcare. We never settle for “good enough” when there’s an opportunity to make life better. Where purpose comes to life, it changes lives. That’s what we live for.

Fluor and Energy Materials, an Orbia business, is seeking a 152a Medical Products Laboratory Analyst (18 months FTC) based at The Heath Technology Park/Rocksavage, UK.

Main Purpose

To provide Medical Products manufacturing, packing operations, and customer support with a Quality Control analysis service to ensure process control, product quality, and compliance with current Good Manufacturing Practice (cGMP) requirements.

This is initially a day role during training, with potential to work on shifts later. Shift pattern: 7am – 7pm, 4 days on followed by 8 days off. Night shifts may be required.

Please note: This is a Fixed Term Contract for 18 months.

Main Responsibilities

• Accurately analyze, validate, and record results for samples from the medical products operation to ensure process control and product quality within specification limits.
• Review and validate analyses performed by other analysts in line with operational requirements.
• Prioritize work to meet production, sales, and customer support goals.
• Investigate abnormal results and report findings to the Medical Quality Control Team Leader, production, or Quality Assurance departments.
• Maintain laboratory, processes, and analysis equipment in compliance with cGMP standards.
• Ensure all sample, analysis, and testing work complies with written procedures, cGMP, and SHE standards.

Qualifications

• Minimum: HNC/HND in Chemistry.
• Desirable: Degree in Chemistry or related field.

Knowledge/Experience Required

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

Behaviors for Success at Orbia:

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

We welcome purpose-driven individuals who are dreamers, doers, and builders. If you’re ready to bring your skills and perspectives to advance your career, the company, people, and the planet, we want to hear from you.

We value every voice, community, and perspective. We are committed to creating a diverse, inclusive, and equitable workplace that supports all employees, regardless of role, location, or background.