You will lead quality oversight for the trading partner wholesaling operations and quality assurance activities across the global supply chain. You will work with internal teams and external partners to set clear quality expectations, manage inspection readiness, and identify and mitigate risks across the supply chain. We value collaborative leaders who can build capability, use data to make decisions, and bring clarity to complex quality issues. This role offers growth, meaningful impact and a chance to help 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.
Responsibilities
* Lead quality oversight for our wholesaling operation across internal and external partners for API/drug substance and drug product between sites and out to customers.
* Define and deploy consistent quality standards, quality agreements and oversight models for the trading partner operations.
* Maintain all the trading partner wholesaling licences, own inspection readiness and coordinate regulatory interactions and responses with stakeholders.
* Use quality metrics and trend analysis to drive continuous improvement across the operation.
* Lead cross-functional working groups to deliver corrective/preventive actions, capability-building and implementation of risk-based controls.
* Coach and develop colleagues and partners to strengthen capability and embed a culture of quality and inclusion.
Qualifications
* Degree in a science, engineering or related discipline, or equivalent experience.
* Minimum eight years' experience in pharmaceutical or biotech quality, including work with external manufacturers or suppliers.
* Solid knowledge of Good Manufacturing Practice (GMP), Good Distribution Practice (GDP) and regulatory expectations in major markets.
* Experience leading audits, inspections, or supplier oversight programmes.
* Proven experience managing cross-functional projects and influencing senior stakeholders.
* Strong communication skills and experience using data to drive decisions.
* Advanced degree (MSc, MBA or equivalent) in a relevant discipline.
* Experience developing quality agreements and supplier governance frameworks.
* Prior experience managing responses to regulatory observations and inspection hosting (particularly MHRA, HPRA).
* Familiarity with global supply networks and commercial third-party manufacturing models.
* Track record of building capability through coaching, training and knowledge transfer.
* Experience with digital quality tools, metrics dashboards or analytics to support risk-based oversight.
Equal Opportunity Employer
GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
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