QA Specialist - GSK0JP00106784

SRG; Stevenage; Hybrid; GBP 60,000 - 80,000; Full time

Job summary

A leading recruitment agency is seeking a BioCTL QA Specialist to support the timely release of medicines in Stevenage. The role includes reviewing QC data, supporting teams, and maintaining high documentation standards. Candidates should have a degree in a scientific field and two years of experience in a regulated environment. This position offers a pay rate of £20 per hour and a hybrid work model after training on a 6-month contract.

Qualifications

• 2 years previous experience in a regulated environment, ideally GMP.
• Laboratory experience is advantageous.

Responsibilities

• Review, approve, and issue QC data to support timely release of medicines.
• Coach and support teams to improve quality performance.
• Perform document control activities.
• Assist in audit and inspection preparation.
• Author GMP documents and maintain documentation standards.
• Initiate quality events and participate in investigations.

Skills

Strong analytical and data interpretation skills

Proficiency in Microsoft Office

Excellent written English

Education

Bachelor of Science (or equivalent experience) in Science, Engineering, or a technical discipline

Job description

Overview

BioCTL QA Specialist Location: Stevenage Pay Rate: £20 per hour Hybrid work available after training 6 Month Contract - maternity cover

Responsibilities

• Review, approve, and issue QC data to support the timely release of medicines.
• Coach and support teams to improve Right First-Time performance.
• Perform document control activities, including controlled printing, reconciliation, and archiving.
• Assist in audit and inspection preparation and participation.
• Author GMP documents and maintain high documentation standards.
• Initiate and participate in quality events, including deviation investigations and change controls.
• Participate in GEMBA walks and process confirmations to drive compliance and efficiency.

Scope & Accountability

Direct Reports: None
Indirect Reports: None
Budget/Revenue Responsibility: N/A

Required Skills & Experience

• Education: Bachelor of Science (or equivalent experience) in Science, Engineering, or a technical discipline.
• Experience: 2 years previous experience in a regulated environment, ideally GMP, in a Quality or Manufacturing support role. Laboratory experience is advantageous.
• Skills: Strong analytical and data interpretation skills.
• Proficiency in Microsoft Office.
• Excellent written English.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy