Associate Principal QA Specialist – Technical Operations

JR United Kingdom; Slough; Hybrid; GBP 40,000 - 60,000; Full time

Job summary

A global biopharmaceutical company is seeking an Associate Principal QA Specialist in Slough. The role involves reviewing GMP quality records, coaching on best practices, and driving compliance initiatives within a hybrid working model. Ideal candidates will have a solid scientific background and experience in quality assurance.

Benefits

Hybrid working model

Hands-on experience in GMP operations

Career growth under senior leadership

Qualifications

• Experience with GMP regulations and documentation approval.
• Proactive and able to thrive in a collaborative environment.

Responsibilities

• Reviewing and approving quality records including deviations and CAPAs.
• Driving continuous improvement initiatives.
• Supporting audit readiness.

Skills

Scientific background

Decision-making skills

Problem-solving skills

Communication

Job description

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Associate Principal QA Specialist – Technical Operations, slough

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Client:

i-Pharm Consulting

Location:

slough, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

2

Posted:

31.05.2025

Expiry Date:

15.07.2025

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Job Description:

Associate Principal QA Specialist – Technical Operations

Location: Slough, UK (Hybrid after initial period onsite)

Contract Type: 12-month contract (INSIDE IR35)

Working Hours: Monday to Friday, 37.5 hours/week

Are you ready to take the next step in your Quality Assurance career?

Our client, a global biopharmaceutical leader, is looking for an Associate Principal QA Specialist to join their dynamic team in Slough. This is a fantastic opportunity for an ambitious QA professional with GMP experience to broaden their exposure in a fast-paced, science-led environment.

What’s in it for you?

• Hybrid working model – initial training onsite, then up to 2 days a week from home
• Hands-on experience supporting GMP operations and major quality systems
• Exposure to cross-functional teams in a thriving biomanufacturing environment
• Grow your career under experienced senior QA leadership

What you'll be doing:

• Reviewing and approving quality records – deviations, CAPAs, change controls and more
• Identifying and driving continuous improvement initiatives
• Coaching business partners on GMP best practices
• Supporting audit readiness and maintaining high compliance standards
• Acting as a QA subject matter expert across site operations

Who we’re looking for:

• A proactive QA professional with a scientific background
• Prior experience approving deviations, CAPAs, and other GMP documentation
• A strong communicator with solid decision-making and problem-solving skills
• Someone who thrives in a collaborative and fast-moving environment

If you’re eager to develop your QA career within a global business, this could be the role for you.

Apply today to be considered for this exciting opportunity!

Please note: You must be able to work in the UK without restriction or sponsorship to be eligible for this role. If you are interested in finding out more about this role or others, please contact Jada Kirlew at [emailprotected] or call: [phone] (UK) / [phone] (NL)