Associate Principal QA Specialist – Technical Operations

i-Pharm Consulting; Slough; Hybrid; Full time

Job summary

A leading company in the life sciences industry is seeking an Associate Principal QA Specialist to enhance quality assurance operations in Slough. This role offers a hybrid working model, hands-on experience in GMP operations, and opportunities for career growth under senior QA leadership. Ideal candidates should possess a scientific background and prior experience in quality documentation.

Benefits

Hybrid working model

Hands-on experience in GMP operations

Exposure to cross-functional teams

Career growth opportunities

Qualifications

• Proactive QA professional with GMP experience.
• Prior experience approving deviations, CAPAs, and GMP documentation.
• Strong communicator with decision-making skills.

Responsibilities

• Reviewing and approving quality records including deviations and CAPAs.
• Identifying and driving continuous improvement initiatives.
• Coaching business partners on GMP best practices.

Skills

Problem-solving

Communication

Collaboration

Education

Scientific background

Job description

Associate Principal QA Specialist – Technical Operations

Associate Principal QA Specialist – Technical Operations

1 day ago Be among the first 25 applicants

Direct message the job poster from i-Pharm Consulting

Providing expert temporary talent solutions for the life sciences industry, with a specialised focus on Quality Assurance and Technical Operations

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 [e-mail] or call: [phone] (UK) / [phone] (NL)

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance and Science

• Industries

  Pharmaceutical Manufacturing and Biotechnology Research

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