QC Analyst

Talentmark; Swindon; On-site; GBP 17,000 - 22,000; Full time

Job summary

Talentmark are recruiting a QC Analyst to join a global healthcare provider to hospitals, clinics and homes on a contract basis for 6 months. This role is fully site based in Swindon.

The company seeks a scientist with hands-on cGXP lab experience, capable of performing finished product QC testing, supporting batch release and generating data using diverse techniques. UK work entitlement is essential and a DBS check may be required.

Qualifications

• Hold a scientific degree or have equivalent working experience.
• Hands-on experience of working in a cGXP lab environment.
• Working knowledge of HCPL Empower, method development, troubleshooting and validation.
• Any experience in the pharmaceutical industry would be an advantage.

Responsibilities

• Conduct Finished Product QC release testing as required.
• Support commercial batch release.
• Conduct QC testing using a range of techniques such as Balances, pH meter, UV, Karl Fischer, FT-IR, TLC and Dissolution.
• Perform analytical work with average testing volumes/output whilst generating data.
• Write and review SOPs and technical reports.

Skills

cGXP lab experience

data generation

SOP writing

Education

Bachelor’s degree in a scientific field

Tools

Empower

Job description

Talentmark are recruiting for a QC Analyst to join a global healthcare provider to hospitals, clinics and homes on a contract basis for 6 months. This role is fully site based in Swindon.

The Company:

Our client is the global leader in enabling pharma, biotech, and consumer health partners to optimise product development, launch, and full life-cycle supply for patients around the world. They have the goal of putting patients first and to help people around the world live better and healthier lives.

Salary:

£13.85 ph PAYE

QC Analyst Role:

• Conduct Finished Product QC release testing as required.
• Support commercial batch release.
• Conduct QC testing using a range of techniques such as Balances, pH meter, UV, Karl Fisher, FT-IR, TLC and Dissolution.
• Perform analytical work with average testing volumes/output whilst generating data.
• Write and review SOPs and technical reports.

Your Background:

• Hold a scientific degree or have equivalent working experience.
• Hands-on experience of working in a cGXP lab environment.
• Working knowledge of HCPL Empower, method development, troubleshooting and validation.
• Any experience in the pharmaceutical industry would be an advantage.

It is essential that applicants hold entitlement to work in the UK

Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check