Scope:Supervising the OQ activities related to the release of manufactured batches, ensuring compliance with Good Manufacturing Practices (GMP), Corporate Quality Standards, and local/international regulations. The role ensures the execution and continuous improvement of quality systems, deviation investigations, audit readiness, and operational quality oversight across the Value Stream.
Key Responsibilities:In this role, you will be responsible for the following:
Quality Oversight & Compliance
Quality Systems & Performance Management
Batch Release & Authorized Person Responsibilities
Leadership & Team Development
Why you?Basic Qualifications:We are looking for professionals with these required skills to achieve our goals:
*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.
This role is fully on site.Application Closure Date: 17 November 2026Please submit your CV in English.*Please take a copy of the Job Description, as this will not be available post closure of the advert.
When applying for this role, please use the ‘cover letter’ of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application.*SkillsData Integrity, Detail-Oriented, Digital Fluency, GxP Regulations, Influencing Without Authority, Lean Management, Pharmaceutical Regulatory Compliance, Problem Solving, Quality Assurance (QA), Risk Awareness, Technical Writing
**Why GSK?
Uniting science, technology and talent to get ahead of disease together.**GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
Contact information:You may apply for this position online by selecting the Apply now button.
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