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Principal QA Specialist

RBW Consulting LLP

Slough

On-site

GBP 40,000 - 80,000

Full time

22 days ago

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Job summary

An established industry player is seeking a Principal QA Specialist for a 12-month contract. This role requires extensive pharmaceutical experience, particularly in quality assurance, to oversee critical quality functions in a fast-paced commercial manufacturing environment. As a subject matter expert, you will be responsible for SQC preparation, deviation tracking, and risk management. This is an excellent opportunity to showcase your skills and potentially open doors for future opportunities within the organization. If you thrive in a dynamic setting and are passionate about quality assurance, this role is perfect for you.

Qualifications

  • Erfahrung in der pharmazeutischen Qualitätssicherung in einem GMP-Umfeld.
  • Fähigkeit, in einem schnelllebigen, kommerziellen Fertigungsumfeld zu arbeiten.

Responsibilities

  • SQC-Vorbereitung und Veröffentlichung sowie Abweichungsverfolgung.
  • Verwaltung von Abweichungskategoriegrenzen und Risikomanagement.

Skills

Pharmaceutical Quality Assurance
Statistical Reporting
Deviation Tracking
Quality Risk Management
Stakeholder Management

Job description

Principal QA Specialist

We are partnered with a leading, global CDMO that is looking to hire an experienced senior quality assurance professional for a 12-month contract. You will use your established pharmaceutical experience to take on a subject matter expert function across key quality functions including but not limited to:

  1. SQC preparation and publishment
  2. Deviation process tracking and reporting
  3. Managing deviation Event Category Limits
  4. Risk management process

Given the nature of the environment, you will have the experience (or at least capability) to deal with a fast paced, commercial manufacturing setting.

As this is a maternity cover contract, there are no guarantees for extension although other opportunities may become available. Therefore, this is a great opportunity to get into the business and prove your worth.

Please contact Mark Bux-Ryan for further information.

Key experience:

  1. Previous pharmaceutical quality assurance experience in a GMP setting
  2. Confident and experienced across statistical reporting, deviation tracking and quality risk management
  3. Excellent stakeholder management skills
  4. Experience and capability of being the subject matter expert in a demanding, client-focused, commercial manufacturing setting
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