Our Client, a Pharmaceutical Manufacturer, Located Close to Watford has a Requirement for a Quality Risk Management Specialist on a 6 Month Fixed Term Basis. The Successful Candidate will Deliver Targeted Quality Risk Management, (QRM), Activities within Defined Projects or Timeframes.
The Role Focuses on Rapid Identification, Assessment, Mitigation, and Communication of Quality Risks, Consistent with GMP and ICH Q9. Activities Support Business‑Critical Initiatives eg Product Launches, Remediation Programmes, and Regulatory Readiness, Including Areas such as Data Integrity and Excipient Risk
ROLE
* Risk Assessment
* Risk Mitigation and Remediation
* Data and Reporting
* Project and Cross‑Functional Support
* Inspection Readiness
* Documentation
REQUIRED
* Degree in Life Sciences, Pharmacy, Chemistry, or Related Field
* Strong Experience in Pharmaceutical Quality and Risk Management
* Sound Knowledge of GMP and Quality Risk Frameworks
* Experience Implementing Risk Processes Across Multi‑Functional Organisations
* Experience with Non‑Sterile Oral Solid Dosage Forms
* Proven Delivery of Training and Stakeholder Presentations
* Strong Understanding of Quality Systems and Compliance
* Rapid Risk Identification and Analytical Problem‑Solving
* Strong Organisation, Prioritisation, and Time Management
* Clear, Concise Communication with Senior Stakeholders
* Adaptable and Delivery‑Focused in Fast‑Paced Environments
* Excellent Written and Verbal English
* Strong Report Writing and Presentation Skills
* Proficient in Microsoft Office Suite
* Experience of Project Management