Ireland - Cork, Belgium-Wavre, Ireland - Dublin, Philadelphia Walnut Street, UK – London – New Oxford Street, USA - Massachusetts - Waltham
Posted on Apr *******
Sterility Assurance Excellence Lead (Senior Director)
Our global supply chain is critical to manufacturing and supplying reliable, high-quality medicines and vaccines to meet patients' needs.
It includes 37 medicines and vaccines manufacturing sites that help make a positive impact on the health of millions of people.
Supply chain teams are part of how we prevent and change the course of disease, bringing our innovations to patients as quickly, efficiently and effectively as possible.
They're involved early in product and process development, working with R&D to make sure that what works in clinical trials can be scaled up to commercial production.
Technology is transforming how we manufacture, enabling increased speed, quality and scale.
We use data to monitor production in real-time, spot ways to increase yields and predict maintenance needs.
Smart manufacturing technologies deliver greater efficiency, productivity, sustainability and cost savings.
As the Sterility Assurance Excellence Lead (Senior Director), you will provide outstanding leadership in shaping and delivering a global sterility strategy across Engineering, QA, Business Units and MSAT.
You will drive standardisation, implement robust risk controls, and ensure inspection readiness across GSK's network and end-to-end business processes, positively impacting quality and compliance.
Key Responsibilities
Own and deploy sterility assurance strategy, standards, and governance to ensure compliance to regulatory expectations.
Lead cross-functional alignment and risk mitigation across Engineering, QA, and MSAT.
Ensure contamination control strategy is standardized and embedded in QMS.
Oversight of facility design and equipment reliability aligned with sterility assurance requirements.
Lead cleaning validation, process control, and supplier qualification as it relates to sterility assurance standards.
Ensure QMS integration, deviation management, and inspection readiness.
Chair monthly governance forums and drive strategic decisions.
Build capability through Communities of Practice.
Strategic Objectives
Accountable for transformation of sterility assurance global standards across Engineering, MSAT and Quality and ensuring that they are in use across all sites.
Set vision for the future to proactively meet regulatory expectations.
Accountable for program management for execution / implementation to global standards.
Deliver Annex 1 compliance through standardized global policies.
Implement KPI dashboards for contamination control and cleaning validation.
Define clear project and governance frameworks to clarify roles and responsibilities between global and local teams.
Drive continuous improvement and proactive inspection readiness.
Lead the uplift in capability building and leadership development across functions.
External network/advocacy with industry forums and regulators to keep pace with evolving regulatory expectations and emerging technology.
Basic Qualifications
Bachelor's degree in microbiology, life sciences, engineering, or related field, or equivalent experience.
Significant experience in sterility assurance, microbiology, or quality in a regulated manufacturing environment.
Proven leadership in cross-functional roles including QA, Engineering, and MSAT.
Strong knowledge of Annex 1, GMP, and global regulatory requirements.
Experience in inspection readiness.
Excellent communication, governance, and stakeholder management skills.
Preferred Qualifications
Advanced degree in microbiology, pharmaceutical sciences, or engineering.
This role can be based at one of our manufacturing sites in the US (East coast), Europe or UK.
Annual base salary ranges from $207,075 to $345,125 for employees based in Cambridge, MA; Waltham, MA; Rockville, MD; or San Francisco, CA.
Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave.
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.
#J-*****-Ljbffr