# Validation Specialist

**Company**: GlaxoSmithKline (GSK)
**Location**: Singapore
**Work arrangement**: onsite
**Experience**: senior
**Job type**: full-time
**Category**: Manufacturing
**Industry**: Healthcare

**Apply**: https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/Singapore---Tuas/Senior--QA-Validation-Executive--1--Year-Contract-_447647-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_c2822819-7ce

## Description

As a Validation Specialist at GSK's Singapore site, you will support and lead validation activities for major projects, ensuring compliance with quality systems and working closely with manufacturing and cross-functional teams. The role involves providing QA oversight for validation projects, authoring and reviewing validation plans, protocols, and reports, and acting as a QA approver for deviations and change controls.

Responsibilities:

- Provide QA oversight for validation projects covering cleaning validation and process validation strategy and execution

- Author, review, and approve validation plans, protocols, reports, and related SOPs

- Assess validation impact for changes, deviations, and investigations

- Act as QA approver for deviations, CAPAs, change controls, and SOPs

- Provide subject-matter expertise to cross-functional teams on validation strategy and execution

- Support preparation of validation documentation and respond to technical queries for product submission

- Apply up-to-date knowledge of regulatory guidance and ensure validation practices reflect industry best practice

Requirements:

- Bachelor's degree in science, engineering, or a related discipline

- Minimum 5 years' experience in pharmaceutical quality assurance, validation, or related roles

- Practical knowledge of current Good Manufacturing Practice (cGMP) and regulatory requirements

- Experience in authoring and approving validation documents and SOPs

- Experience in assessing impact of changes, deviations, and corrective actions on validation status

- Strong communication skills with the ability to work effectively across stakeholders of different functions

Preferred Qualifications:

- Experience with equipment and computerized system validation

- Prior role involved in validation strategy for new product introduction or technical transfer projects

- Project management experience and familiarity with continuous process verification approaches

- Practical understanding of quality management systems and audit processes

## Skills

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

### Nice to have
- Equipment and Computerized System Validation
- Project Management
- Continuous Process Verification
- Quality Management Systems
- Audit Processes

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Source: [Apply at gsk.wd5.myworkdayjobs.com](https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/Singapore---Tuas/Senior--QA-Validation-Executive--1--Year-Contract-_447647-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)