QA Associate

SRG; Slough; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading staffing agency is seeking a QA Associate in Slough. The role involves batch consolidation for QC activities in drug product testing and requires attention to detail and proficiency in MS Office. Ideal for entry-level candidates, this position offers a pay rate of £21.92 per hour and is fully onsite for a 9-month contract.

Qualifications

• Entry-level position; prior QA/GMP experience is beneficial but not essential.

Responsibilities

• Perform Batch Consolidation for QC Biochemistry and Microbiology testing.
• Ensure all testing activities meet release specifications.
• Issue GMP documents and labels to Manufacturing.
• Support QA Operations in quality systems improvement.

Skills

Strong attention to detail and accurate data entry

Proficiency in MS Office (Word, Excel, Outlook, Access)

Effective verbal and written communication

Risk-based decision-making

Strong organisational and planning skills

Education

BSc in Biology or a related field (or equivalent experience)

Job description

Overview

QA Associate – Location: Slough (Fully Onsite)

Contract Length: 9 months (with potential to extend)

Pay Rate: £21.92 per hour

Role Purpose & Scope

As a member of the QA Operations Documentation Control Team, your primary responsibility will be to perform Batch Consolidation (auditing) for QC Biochemistry and Microbiology testing activities related to Drug Product (DP) and Drug Substance (DS). You will ensure all QC testing activities are complete and meet release specifications. You will also proactively issue GMP documents and labels to Manufacturing in line with schedules and timelines.

Key Responsibilities

• Coordinate and perform batch consolidation for QC Biochemistry and Microbiology testing.
• Ensure all testing activities are complete and meet release specifications.
• Issue GMP documents and labels to Manufacturing, ensuring accuracy and timeliness.
• Liaise with internal departments to gather required information and maintain effective communication.
• Support QA Operations in continuous improvement of quality systems and processes.
• Assist in audit preparation and provide documentation during audits.
• Lead and manage quality records (Deviations, CAPAs, Change Controls, Investigations).
• Author, review, and approve GMP documentation.
• Maintain the archiving system and coordinate document retrieval.
• Ensure training compliance and maintain an up-to-date training profile.
• Prioritise workload to meet strict deadlines and support Manufacturing needs.
• Perform other duties as assigned.

Key Stakeholders

• Quality Control
• Manufacturing
• Quality Assurance & Qualified Persons (QPs)

Required Skills & Competencies

Technical & Interpersonal Skills

• Strong attention to detail and accurate data entry
• Proficiency in MS Office (Word, Excel, Outlook, Access)
• Familiarity with database systems
• Effective verbal and written communication
• Risk-based decision-making
• Ability to prioritise workload and meet deadlines
• Strong organisational and planning skills
• Experience with PQS (Pharmaceutical Quality Systems) is desirable

Core Competencies

• Agility – Learns from experience, adapts to change, and embraces new challenges
• Business Acumen – Understands how their role contributes to business success
• Collaboration – Shares knowledge, listens actively, and respects others
• Customer Focus – Understands and responds to internal/external customer needs
• Driving Results – Delivers high-quality work on time, monitors KPIs, and overcomes challenges
• Leadership – Takes responsibility, seeks feedback, and contributes to a positive work environment

Qualifications

• Education: BSc in Biology or a related field (or equivalent experience)
• Experience: Entry-level (0-4 years); prior QA/GMP experience is beneficial but not essential

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