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Eblex Group

Director Clinical Quality Assurance

London
£100k – £125k/yr
Posted about 18 hours ago
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Director Clinical Quality Assurance with GMP Exposure

Eblex Group is supporting a growing biotechnology company with an expanding clinical pipeline in the search for a Director Clinical Quality Assurance with GMP exposure.

This is a broad QA role within a lean biotech environment, working closely with Clinical Development and other functions across clinical quality, audits, CAPA, investigations, QMS and inspection readiness.

Key Responsibilities of the Director Clinical Quality Assurance

  • Provide QA oversight across clinical development programmes
  • Support GCP compliance, quality risk management and inspection readiness
  • Manage clinical audit programmes and coordinate internal and external audits
  • Review and manage CAPAs, deviations and quality investigations
  • Support the company's eQMS, including controlled documents, training and quality events
  • Provide QA input into clinical documentation and regulatory activities
  • Monitor changes to ICH GCP, MHRA, FDA and EMA requirements
  • Support regulatory inspections and audit preparation
  • Provide QA input into partnerships, due diligence and licensing activities

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Graduate Consultant — 2026 Scheme

PwC·London, UK
£35,000/yr

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Your economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.

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You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.

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What We're Looking For in a Director Clinical Quality Assurance

  • 5+ years' experience within biotech or pharma
  • 3+ years' experience in GCP Quality Assurance
  • Strong understanding of ICH GCP and global clinical trial regulations
  • GMP exposure
  • Experience with eQMS platforms, ideally Veeva
  • Experience supporting MHRA, EMA or FDA inspections
  • Strong experience with audits, CAPAs, deviations and investigations
  • Early phase or highly regulated therapeutic areas.
  • Comfortable working independently within a growing biotech

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This is a great opportunity for a hands on QA professional who is looking to take ownership and visibility within a growing clinical development organisation.

Eblex Group is managing this search exclusively.

Apply directly or contact us for a confidential discussion.

Clinical Quality | Good Clinical Practice | Biotech | Quality Assurance | Director Clinical Quality Assurance | GCP | Clinical | Global | Early Phase | Late Phase | Clinical Development

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Skills

Clinical Quality Assurance
GCP Compliance
GMP
Quality Risk Management
Inspection Readiness
Clinical Auditing
CAPA Management
Quality Investigations
eQMS
Veeva
Regulatory Compliance
Due Diligence

Location

London, England, United Kingdom

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