# Quality Oversight Supervisor

**Company**: GSK
**Location**: Cairo, Egypt
**Work arrangement**: onsite
**Experience**: senior
**Job type**: full-time
**Category**: Operations
**Industry**: Healthcare

**Apply**: https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/Egypt---Cairo/Operation-Quality-Section-Head_450960?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/quality-oversight-supervisor-13604fd4-b13/

## Description

We are seeking a Quality Oversight Supervisor to supervise OQ activities related to the release of manufactured batches, ensuring compliance with Good Manufacturing Practices (GMP), Corporate Quality Standards, and local/international regulations.

**Key Responsibilities:**

- Drive and strengthen quality culture across all value stream operations.

- Define and maintain the scope and risk-based frequency of Quality Oversight activities across manufacturing, processing, packaging, and supporting functions.

- Supervise OQ Officers in executing routine oversight activities and ensuring GMP compliance.

- Monitor oversight coverage, execution, overdue activities, and related actions.

- Evaluate oversight effectiveness and drive continuous improvement.

- Ensure implementation and compliance with site QMS, GMP, GMS, and regulatory requirements.

**Quality Systems & Performance Management:**

- Lead and oversee deviations, OOS/OOT investigations, complaints, CAPAs, quality incidents, rework, and reprocessing activities, ensuring robust investigations and timely closure.

- Drive quality performance improvement through monitoring of site KPIs, quality trends, periodic system reviews, and Quality Improvement Programs (QIPs).

- Prepare and present periodic quality performance and system reviews to the Site Quality Council.

- Review and approve relevant quality risk assessments, product lifecycle activities, validation documents, and periodic product reviews.

- Manage and coordinate product quality incidents with relevant site quality functions.

- Drive inspection readiness through GEMBAs, SLE activities, and support of GPS foundations.

- Escalate critical quality issues and ensure effective resolution.

**Batch Release & Authorized Person Responsibilities:**

- Oversee and perform batch release activities for manufactured and packaged products, ensuring full GMP and regulatory compliance.

- Review and approve batch documentation, including BMRs, BPRs, specifications, BOMs, and relevant quality records.

- Ensure completion and assessment of all required manufacturing, QC, sampling, testing, change control, and deviation activities before batch release.

- Perform Authorized Person batch release activities and relevant ERP transactions, including release, rework, and rejection decisions.

- Oversee AP delegate qualification, where applicable.

- Monitor and report conformance to release plan and maintain accurate SAP quality-related data.

**Leadership & Team Development:**

- Lead, coach, and develop direct reports, ensuring appropriate technical competencies, training, and qualifications.

- Monitor team performance and promote accountability, collaboration, and continuous improvement.

- Build effective cross-functional partnerships to achieve site quality objectives.

**Requirements:**

- University Degree in Pharmacy or Scientific disciplines.

- Minimum five years of experience in Quality Assurance, or Operational roles within the Pharmaceutical industry.

- Previous people management experience.

- Fluency in English and Arabic (both written and spoken).

**Key Capabilities and Skills:**

- Up to date knowledge of current GMP, EDA Regulatory requirements, QMS System.

- Excellent documentation, report writing skills, and computer skills.

- Excellent verbal and written communication skills.

- Excellent problem solving and critical thinking capabilities.

- Strong prioritization and organization skills.

- Familiar with IQ, OQ, PQ, facility, utilities, Equipment and Strong experiences in cGMP/GLP compliance activities.

- Self-motivation, empowerment and adaptation to business changes.

- Able to demonstrate experience of managing diverse teams of professional staff and effective budgetary control against agreed targets.

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## Skills

### Required
- GxP Regulations
- Pharmaceutical Regulatory Compliance
- Quality Assurance (QA)
- Risk Awareness
- Technical Writing
- Lean Management
- Influencing Without Authority
- Problem Solving
- Data Integrity
- Digital Fluency
- Arabic

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