Hello. We're Haleon, a new world-leading consumer health company. Shaped by all who join us. Together, we improve everyday health for billions of people. By growing and innovating our global portfolio of category-leading brands – including Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum – through a unique combination of deep human understanding and trusted science.
This is an exciting time to join us and help shape the future. It's an opportunity to be part of something special.
About the Role
* Lead internal audits of GSK Nyon plant departments to identify non-compliance with GSK QMS, National/International GxP requirements, and Local Standard Operating Procedures.
* Local process owner for self-inspection, internal and external audits.
* Inspection Readiness process: support Inspection/Audit of Nyon plant by Health Authorities, GSK group (CAG, A&A), Customers, and Notified Body (SQS). Prepare audit and Inspection answers. Follow action plan and document action closure.
* Manage Documentation and training activities.
Key Responsibilities
SELF INSPECTION
Local process owner of the Self-Inspection process: define SOP and template according to Global CH guidance, define training program and train designee associate, review and approve audit universe, define and report KPls, trends findings, and escalate any significant gaps.
INTERNAL AUDIT
Local process owner of the Internal Audit process: define SOP and template according to Global CH guidance, define training program and train designee associate, define internal audit universe and internal audit program in collaboration with the QA Release, Compliance, and Auditing Senior Manager, conduct internal audit, issue report, approve proposed CAPA, follow CAPA closure on time, define and report KPls, trends findings, and escalate any significant gaps.
EXTERNAL AUDIT
Local process owner of the External Audit process for Nyon site services providers not integrated in the SQA&C program. Define SOP and template according to Global CH guidance, define training program and train designee associate, define audit universe and external audit program with the QA Release, Compliance, and Auditing Senior Manager, conduct external audit, issue report, approve proposed CAPA, follow CAPA closure on time, define and report KPls, trends findings, and escalate any significant gaps.
GSK AUDIT / HA INSPECTION CUSTOMERS AUDIT
Support the QA Release, Compliance, and Auditing Senior Manager for audit/inspection organization. Review and approve, in collaboration with QA Release, Compliance, and Auditing Senior Manager, proposed corrective/preventive action plans.
CAPACITY MANAGEMENT
Manage CAPA follow-up in accordance with Global CH guidance and local SOP.
SITE TRAINING
Design, deliver, implement, and maintain a comprehensive training program for the Nyon manufacturing plant for compliance-based and priority training initiatives to include GMP, EHS, technical production skills, regulatory compliance, and new employee onboarding.
CONTINUOUS IMPROVEMENT
SME for Auditing process. Author and review Standard Operating Procedures as needed. Complete Lessons Learned and share Best Practices resulting from audits/inspections in Nyon plant.
DOCUMENTATION MANAGEMENT
Oversee the design, delivery, development, and renewal of the site's documentation program, including both hard copy and electronic documentation. Ensure that associated documentation (SOPs, Forms, protocols, reports, etc.) are governed by a clear, simple, and appropriate process.
PEOPLE MANAGEMENT
People management of direct reports which are both independent contributors as well as managers of other associates (e.g., SME of PIR).
GMP and HSE
Respect all GxP standards and HSE requirements at Nyon plant. Ensure associates respect local GxP and HSE requirements and escalate any significant issue observed.
Qualifications and Skills
Essential
* University degree in Quality Assurance, Pharmaceutical Technology, Chemistry, Pharmacy, or equivalent scientific degree.
* Pharmaceutical industry specialization.
* Minimum 5 years of experience in the pharmaceutical industry within the quality assurance function.
* Experience in auditing activities.
* Haleon/GSK certified auditor.
* Good interpersonal and leadership skills.
* Safety, Quality, Results, and Customer-oriented.
* Previous people management experience (either direct or indirect).
* Fluency in French and English.
* Excellent knowledge of GMP and regulatory expectations.
* Excellent communication skills.
* Ability to influence people.
* Role model in GxP, HSE, and Haleon values expectation.
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Diversity, Equity, and Inclusion
We embrace our diverse workforce by creating an inclusive environment that celebrates our unique perspectives, generates curiosity to create unmatched understanding of each other, and promotes fair and equitable outcomes for everyone.
We're striving to create a climate where we celebrate our diversity in all forms by treating each other with respect, listening to different viewpoints, supporting our communities, and creating a workplace where your authentic self belongs and thrives.
We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.