Senior Quality Manager Gcp Job In Cambridge

Working as a Senior Quality Expert/Manager - GCP, you will act as the advisor to the Clinical Development teams on all quality related GCP activities. This will be an exciting opportunity with a clinical-stage biopharmaceutical company with multiple Phase 3 assets.

Key Responsibilities:

• To play a key role in maintaining and monitoring the GxP QMS ensuring it meets all regulatory requirements and standards, with emphasis on GCP compliance.
• To provide support and advice to Clinical Development teams with regards to:
• Definition of appropriate compliant procedures within GxP functions
• Management of quality issues
• To ensure external contracted organisations supporting GxP activities are selected and responsibilities defined and documented.
• To monitor the performance of GxP service providers with regards to the relevant quality standards.
• To define and manage clinical audit programme and to preform GCP audits if required.
• Maintain agreed quality metrics and dashboards to enable clear communication to senior management of compliance performance and any risks or issues identified.
• To maintain awareness of, and ensure compliance with, policies and procedures relating to quality standards within the Company.

Skills/Knowledge Competencies:

• Substantial experience of successfully managing quality issues in a biotechnology or biopharmaceutical environment.
• Proven track record in defining, implementing and maintaining Quality Management Systems for biotechnology or biopharmaceutical companies.
• Proven track record of monitoring and influencing the quality performance of internal functions and contracted service providers, including self-inspection and external audit experience.
• Comprehensive knowledge of GCP requirements as applied to biologics and related industry/regulatory guidelines governing clinical trials in the EU & USA.
• Basic understanding of GLP and GMP requirements for biologics
• Basic Knowledge of GLP and cGMP and related industry/regulatory guidelines governing the manufacture of biologics in the UK, EU & US.
• Ability to work in a flexible, collaborative style with colleagues and teams within the company and with external entities including CROs and consultants.

Experience:

• Minimum 5+ years in a similar role

Salary and benefits:

A highly competitive salary, stock options, annual bonus and wider benefits package is on offer.