GSK
Pharmaceutical
LOCQualityManager
Neural analysis suggests this role is
optimal for Manager candidates.
“LOC Quality Manager at GSK. Skills: Quality Management System, Operational quality, Regulatory compliance. Maintain and operate the local Quality Management System. Review production and batch documentation”
Industry & Context.
Root cause analysis; Investigations; Risk assessments; Change control
What They're Looking For.
Must Have
Bachelor’s degree in Pharmacy, Chemistry, Biology, Engineering or related scientific or equivalent professional qualification, 3 to 5 years’ experience in quality assurance or operational quality in the life sciences or pharmaceutical sector, Practical knowledge of Good Manufacturing Practices and Good Documentation Practices, Experience with batch documentation review, in-process checks and product release support, Experience managing deviations, CAPAs, investigations and quality records, Proficient in MS Office and able to use standard business systems and email
Nice to Have
Bachelor of Pharmacy, Pharm-D, or higher degree in a relevant field, Experience with ERP or quality systems such as SAP or similar, Experience leading self-inspections, internal audits or supporting regulatory inspections, Knowledge of data integrity principles and practical application, Experience working with third-party manufacturers, warehousing or distribution operations, Comfortable working under pressure, Able to manage multiple priorities, Licensed Pharmacist
What You'll Do.
Maintain and operate the local Quality Management System
Review production and batch documentation
Support timely lot release decisions
Support investigations
root cause analysis and corrective actions
Perform self-inspections
Support external audits and regulatory inspections
Monitor quality performance metrics
Drive continuous improvement actions
Coordinate quality activities with third-party providers
Ensure operations follow approved procedures
Ensure records are accurate and complete
Coach production and warehouse teams on good documentation
Manage quality records
retained samples and documentation
Support risk assessments and change control
deviation and complaint management
Prepare for and support internal and external audits
How You'll Work.
Team & Collaboration
Cross-functional teams; Third-party providers; Suppliers
Communication Scope
Collaboration; Communication
Full Job Description
Business Introduction We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it’s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply. We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients. Position Summary You will support operational quality activities at our Philippines site. You will work with the Local Operating Country Quality Manager and cross-functional teams to keep our Quality Management System effective and inspection ready. You will help manage day-to-day quality operations, support investigations, and drive improvements that protect patient safety. We value people who are practical, curious, collaborative and committed to learning. This role offers visible impact, career growth, and the chance to unite science, technology and talent to get ahead of disease together. This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: \- Maintain and operate the local Quality Management System to meet GSK standards, good manufacturing practices and local regulations. \- Review production and batch documentation and support timely lot release decisions. \- Support investigations, root cause analysis and corrective actions for deviations, complaints and audit findings. \- Perform self-
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