Job Title: Network Strategy Quality Director
Job Purpose:
Provide Quality Leadership for network strategy projects that strengthen our supply network. Will work with cross-functional partners in Quality Supply Regulatory and external manufacturers to define and deliver network programs. We value people who are collaborative pragmatic and driven to make measurable improvements. This role offers growth visible impact and the chance to help unite science technology and talent to get ahead of disease together.
Key Responsibilities:
Provide Quality Leadership for strategic projects that improve external quality performance and inspection readiness across contract manufacturing partners.
Ensuring on time delivery of strategy assessments and implementation requirements for network strategies with documented outputs for Quality governance requirements
Design and implement consistent quality standards quality agreements and oversight models for third-party suppliers.
Coordinate risk assessments remediation plans and Corrective Action and Preventive Action (CAPA) oversight with external partners and internal stakeholders.
Drive data-led decision making using quality metrics and trends to prioritise interventions and track outcomes.
Lead cross-functional working groups and provide regular updates to senior governance forums.
Develop capability through coaching training and sharing best practice across network partners.
Basic Qualification:
Experience in pharmaceutical or biotech quality including work with external manufacturers and partners.
Experience in Good Manufacturing Practice (GMP) and regulatory expectations in major markets.
Experience leading cross-functional projects and managing third-party relationships.
Experience in GSK governance and decision-making processes
Preferred Qualification:
Degree in a scientific engineering or related discipline or equivalent experience.
Experience working with contract manufacturing organisations (CMOs) or in a network strategy role.
Prior involvement in regulatory inspections or responses to regulatory observations.
Experience developing quality agreements and supplier oversight frameworks.
Prior involvement and responsibilities for significant strategic programs of work.
Experience with risk-based approaches and quality management systems at scale.
Working Arrangements:
This role offers a hybrid working model with a mix of on-site and remote work.
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 were 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.
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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About us We are a science-led global healthcare company with a special purpose: to help people do more, feel better, live longer. We have 3 global businesses that research, develop and manufacture innovative pharmaceutical medicines, vaccines and consumer healthcare products.