Senior Strategic QA Manager for Oncology Scale-up

SciNova • United Kingdom
Remote
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AI Summary

Drive GMP readiness and inspection readiness for a late-stage Oncology scale-up. Lead Quality leadership and deliver GMP readiness activities. Ensure compliance with GLP/GMP/GCP requirements.

Key Highlights
GMP readiness
Inspection readiness
Quality leadership
Key Responsibilities
Provide strategic Quality leadership across late-stage clinical development and transition to commercialisation.
Lead and deliver GMP readiness activities in preparation for clinical and commercial manufacturing.
Drive inspection readiness and act as a key QA lead for FDA and EMA inspections.
Ensure compliance with GLP/GMP/GCP requirements.
Lead, maintain, and scale the company’s Quality Management System (QMS) to ensure inspection readiness.
Act as a senior QA partner to Clinical, Regulatory, CMC, Supply Chain, and other critical internal stakeholders.
Plan and lead internal audits, mock inspections, health authority inspections, and vendor audits.
Provide mentorship, training and guidance to the existing QA team.
Technical Skills Required
GLP/GMP/GCP Quality Management System (QMS)
Benefits & Perks
Competitive salary
Performance-based bonus
Collaborative and innovative work environment
Excellent professional development and growth opportunities

Job Description


Title: Senior Strategic QA Manager

Location: UK (remote)

Sector: Oncology

Contract: Permanent on a part-time basis or freelancers considered


SciNova are supporting an international late-stage Oncology scale-up who are searching for a Senior QA Strategic Manager during a critical phase of growth. This role will play a central part in driving GMP readiness and preparing the organisation for global health authority inspections, including FDA and EMA. This is a hands-on and strategic position, working closely with c-suite and senior stakeholders to ensure robust, phase-appropriate Quality systems aligned with EU and US regulatory expectations.


The role is fully remote within the UK and offers flexibility through either a freelance engagement or a permanent part-time contract.


Role responsibilities:

  • Provide strategic Quality leadership across late-stage clinical development and transition to commercialisation.
  • Lead and deliver GMP readiness activities in preparation for clinical and commercial manufacturing.
  • Drive inspection readiness and act as a key QA lead for FDA and EMA inspections.
  • Ensure compliance with GLP/GMP/GCP requirements.
  • Lead, maintain, and scale the company’s Quality Management System (QMS) to ensure inspection readiness.
  • Act as a senior QA partner to Clinical, Regulatory, CMC, Supply Chain, and other critical internal stakeholders.
  • Plan and lead internal audits, mock inspections, health authority inspections, and vendor audits.
  • Provide mentorship, training and guidance to the existing QA team.


Role requirements:

  • MSc or PhD in a relevant scientific discipline is highly preferred.
  • Extensive experience in a senior QA position within the Biotech/Biopharma stage leading late stage development (II/III) projects preferably within oncology (other therapeutic areas considered).
  • Demonstrated experience delivering GMP and inspection readiness for FDA and EMA.
  • Experienced in mentoring, guiding and training internal QA professionals.
  • Ability to operate effectively at both strategic and operational levels.
  • Excellent communication skills and confidence engaging with senior leadership and external partners
  • Fluent English.
  • Obtain the right to work in the UK without need for sponsorship.


What my client offers:

  • Competitive salary and performance-based bonus.
  • A collaborative and innovative work environment.
  • Excellent professional development and growth opportunities.
  • Fast-paced scale-up culture.


How to apply:

Send your CV to lauren.howes@scinovasearch.com or apply via LinkedIn.


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