QC Analyst

E3recruitment; Lower Hopton; On-site; GBP 22,000 - 27,000; Full time

Job summary

A global pharmaceutical company in Lower Hopton is seeking a QC Analyst on a 6-month FTC. The role involves analyzing raw materials and finished products, adhering to safety regulations, and maintaining documentation. Candidates should hold a relevant degree and have experience with GC and HPLC techniques. The position offers a salary of up to £27,000 plus a comprehensive benefits package including healthcare and a performance-related bonus.

Benefits

Competitive pension

Private healthcare plan

Performance related annual bonus

Annual pay review

Flexible working opportunity

25.5 days annual leave plus bank holidays

Income protection

Business and personal travel insurance

Life assurance up to 4x base salary

Cycle to work scheme

Qualifications

• Technical laboratory background with proven experience on a GMP site.
• Experience dealing with analytical reports.
• Ability to perform instrumental troubleshooting.

Responsibilities

• Conduct analysis of raw materials and finished products.
• Perform second analyst data checks and routine calibrations.
• Prepare customer samples, standards, and maintain documentation.
• Support laboratory operations through housekeeping and document generation.
• Adhere to COSHH regulations and maintain safe laboratory practices.
• Lead troubleshooting and maintenance of analytical systems.

Skills

GC (Gas Chromatography)

HPLC (High-Performance Liquid Chromatography)

Analytical skills

Education

HNC/HND or degree in Analytical, Chemical or Pharmaceutical subject

Job description

Overview

QC Analyst role working standard days on a 6m FTC (fixed term contract) and paying up to £27,000 (DOE), plus a benefits package including a competitive pension, private healthcare plan, up to 15% performance related annual bonus, annual pay review, flexible working opportunity, 25.5 days annual leave plus bank holidays, income protection, business and personal travel insurance, life assurance up to 4x base salary, cycle to work scheme and more!

This QC Analyst (Quality Control) role is working with a globally leading pharmaceutical manufacturing company which is present in more than 20 countries world-wide and has over 20,000 employees globally. Taking this opportunity as QC Analyst would mean working for a leading global producer of API’s (Active Pharmaceutical Ingredients). This role would include opportunities to advance your career, skillset, and education.

Responsibilities

• As the QC Analyst, you will conduct analysis of raw materials and finished products in line with established SOPs, ensuring accurate interpretation, documentation, and communication of analytical data.
• Hold responsibility for performing second analyst data checks, routine calibrations, and ongoing monitoring of analytical instruments, including basic troubleshooting and maintenance.
• You will prepare customer samples, standards, and all related documentation, maintaining up-to-date analytical databases and spreadsheets.
• In charge of supporting laboratory operations through housekeeping, standard assessments, and document generation or review in compliance with quality requirements.
• You will adhere to COSHH regulations and always maintain safe laboratory practices.
• Lead basic troubleshooting and maintenance of analytical systems

To be successful in this position as QC Analyst

• You will hold either a HNC/HND or a degree in a relevant Analytical, Chemical or Pharmaceutical subject.
• Have an established technical Laboratory background including proven experience of GC (Gas Chromatography) and HPLC techniques.
• Experience in dealing with analytical reports and instrumental trouble shooting on a GMP site is also essential.

Please apply directly for this QC Analyst role.