Quality Issue Lead - Fsp

Parexel; A distancia; MXN 600,000 - 800,000; Jornada completa

Descripción de la vacante

A global biopharmaceutical company in Veracruz, Mexico, seeks an experienced individual to oversee quality event assessments, ensuring timely reviews and escalation of critical issues. The ideal candidate should have extensive pharmaceutical experience, project management skills, and familiarity with GCP standards. This role will contribute to process improvements and CAPA management. Excellent communication and continuous improvement skills are essential for success in this position. The company offers a remote work option.

Formación

• 7+ years of relevant experience with a BS or 6+ years with an MS/MBA.
• Solid experience in pharmaceutical data management and quality.
• Strong background in continuous improvement methodology preferred.

Responsabilidades

• Accountable for review and classification of quality issues.
• Initiates escalation of critical quality events to management.
• Contributes to process development and improvement.
• Holds accountability for CAPA completion and tracking.

Conocimientos

GCP Quality

Data Management

Process Improvement

Regulatory Inspection

Project Management

Educación

Bachelor's degree (7+ years of experience) or Master's/MBA (6+ years of experience)

Descripción del empleo

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.

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