Quality Control Analyst — GMP Lab & Analytics

Nelsons; Greater London; On-site; GBP 27,000 - 42,000; Full time

Benefits offered by this job

Annual bonus

25 days holiday

Staff discounts

Cycle to work

Pensions

Eye care vouchers

Season ticket loan

Volunteer days

Job summary

Nelsons is recruiting a QC Analyst to join the Quality Control team in a fast-paced pharmaceutical environment. You will perform analytical testing on raw materials and finished products using HPLC and GC techniques, maintain data in the QMS, and ensure compliance with cGMP and Data Integrity principles.

Key duties include environmental monitoring, in-process checks, documentation updates, and supporting validation activities. A science degree and laboratory experience are required.

Qualifications

• Degree level or above in a Science subject.
• Experience in an analytical laboratory.
• Ability to use work instructions and specifications for testing of products and raw materials.
• GMP and Data Integrity principles understood.
• Strong report writing skills.

Responsibilities

• Test all incoming raw materials according to in-house specifications and methods of analysis.
• Test finished products according to approved in-house specifications and methods of analysis.
• Carry out environmental monitoring.
• Support validation activities in the lab.
• Carry out line checks on production activities and in-process checks.
• Perform analyses, examinations or investigations as required.
• Contribute to data management and documentation in QMS.

Skills

HPLC techniques

GC techniques

Report writing

GMP/Data Integrity

Analytical lab experience

Education

Degree level or above in a Science subject

Tools

HPLC instruments

GC instruments

Job description

Nelsons is recruiting a QC Analyst to join the Quality Control team in a fast-paced pharmaceutical environment. You will perform analytical testing on raw materials and finished products using HPLC and GC techniques, maintain data in the QMS, and ensure compliance with cGMP and Data Integrity principles.

Key duties include environmental monitoring, in-process checks, documentation updates, and supporting validation activities. A science degree and laboratory experience are required.