Quality Issue Lead

Há 2 dias

Brasília, Brasil Parexel Tempo inteiro

**ROLE RESPONSIBILITIES**:
**Quality Event Assessment and Investigation**

This individual will be accountable for the review and classification of submitted quality issues to ascertain if the QE threshold has been met. He or she will ensure that each submitted issue is reviewed based on the established criteria, is categorized appropriately, and completed within the required time frame to ensure that events are appropriately qualified enabling expedited investigation where necessary. This individual will also be responsible for completing the necessary documentation in the eQMS system regarding the assessment of the submitted events.

**Notification to Management**

This individual will be responsible for initiating appropriate escalation of Critical QEs when necessary, ensuring that management is promptly and appropriately informed of quality events. The Issue Lead will be required to assess critical issues and identify these items as appropriate for escalation to leadership via the Notification to Management process.

**Root Cause Analysis / Gap Analysis / Due Diligence**

**Process Analysis and Improvement**

This individual will be responsible for contributing to process development and improvement for case management including contributing to the development of technology (in collaboration with PFE Digital) to enable the process. In addition, the individual, along with Senior Issue Lead peers, will develop and implement guidance documents and training to assist the investigation leads in completing cases to expectations.

**CAPA Plan Development and Management**

This individual will hold accountability for ongoing monitoring of CAPA completion and tracking of effectiveness for implemented mitigation actions to ensure they are working as expected—for quality events, inspections and audits
- Ensure implementation of QE / audit / inspection CAPAs and remediation plans
- Track effectiveness checks and report on trends

**Risk Mitigation Tracking**

Track and ensure implementation of risk mitigations and evaluate potential impacts to business.

**QUALIFICATIONS**

BS - 7+ years or equivalent

MS/MBA - 6+ years or equivalent

**Previous Experience**:

- Minimum of 5 years of pharmaceutical experience with solid experience in data management, operational aspects, GCP Quality, GxP Quality, and/or regulatory
- Regulatory inspection experience
- Process and system management experience
- Detailed knowledge of clinical trial processes and relationships required
- Knowledge of GCP requirements and applicable SOPs and regulations
- Project management, administrative, and technical capabilities are required, as well as effective verbal and
- Strong background in continuous improvement methodology (i.e., Lean Six Sigma) preferred.

LI-LG4

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