Belgium Job Openings
GSK
Senior Director Quality & Risk Management, Global Health
Wavre
September 2, 2024
Posted Date: Sep 1 2024
Senior Director, Quality & Risk Management, Global Health
The deadline for the job posting is the 15th of September
Background:
Global Health (GH) is a cornerstone of GSK’s ESG agenda, committed to change the trajectory of high burden diseases in lower-income countries with a focus on prevention and treatment of infectious diseases - We are investing £1bn over ten years to accelerate global health R&D.The Global Health ambition is achieved through:
- R&D Developing new vaccines & medicines against high burden infectious diseases in lower-income countries
- Access Pursuing equitable access to GSK’s portfolio & pipeline
- Health System Strengthening Improve health equity for communities who need it most, through catalytic partnerships
Purpose:
The Senior Director, Quality & Risk Management, Global Health partners with the Global Health Leadership team to develop and deliver an effective Quality & Risk Management Program for the Global Health Unit in GSKResponsibilities include:
- Partner with the GH LT to enhance the quality and compliance performance, identifying and managing the inherent and emerging risks associated with the GH Strategy. This requires an understanding of the current level of control within the GH business lines and an understanding of the GH business activities
- Partner with GH Line Leaders to understand and enhance the risk and quality culture so people at all levels of the organization, speak up when concerns, risks or issues occur. Allowing GH to proactively address matters through early mitigation using data to support changes in their Line operations
- Where appropriate, integrate GSK and R&D quality, compliance and risk management policies and programs into the GH business processes and ways of working. Bridge the full GSK enterprise approach to risk and quality management within GH Lines
- Develops and maintain a systematic quality risk management program within the GH lines and at the enterprise level for multiple areas of regulatory risk, including Good Manufacturing Practices, Good Laboratory Practices, Human Biological Samples, Data Integrity, Anti Bribery and Corruption, Data Privacy and Ethical Treatment of Animals, Scientific and Patient Engagement, Human Subject Research as well as interactions with external parties of interest – Regulatory Authorities, CROs, AROs study sites and external partners. This is built through a strong collaborative GH RM Community of practice
- Provide objective leadership for GH on matters arising (planned and unplanned); ensuring that GH’s ‘requirements, needs and interests’ are delivered. This may include and not be limited to leading the GH Grants and Donations Committee (in support of the non-R&D GH requests)
- Embed quality decision making into GH ways of working, ensuring that the Internal Control Framework is integrated and compliant to corporate and regulatory standards by building strong partnerships across the network
- Maintain contemporary knowledge in the evolving regulatory expectations and global environment that impact the business to proactively manage risks and increase the robustness of our business processes and decision making
-
Outputs are deliverables will encompass the expectations of the Internal Control Framework, for example:
- Training: Developing and identifying capability gaps to embed a robust quality and compliance training curriculum
- Risk Assessment: Overseeing the prioritization and escalation of GH line related risks to the GH LT and overseeing the definition and mitigation of GH Enterprise risks
- Management Monitoring: Ensuring a robust management monitoring across GH
- Responding to Problems: Agile problem solving as matters arise in GH
- Communication: Providing an enterprise monitoring perspective of the GH Enterprise Quality and Compliance performance; taking into the performance of business partners (to understand dependencies and impact on GH); through assessment of risk, compliance, and quality trends, facilitate implementation of quality improvements and ensure business critical quality improvements are adequately resourced to deliver. Utilize the learning to help GH drive proactive risk management
- GH Audit readiness, protecting the license to operate
Requirements:
- Bachelors’ Degree from a Global Health, Scientific, or related discipline
- A broad scientific/pharmaceutical industry background
- Knowledge of essential regulatory guidelines, world-wide policies and procedures which impact critical aspects of GH e.g. knowledge ABAC, Sanction, Human Subject Research, Scientific and Patient Engagement
- Demonstrated experience managing and engaging with senior stakeholders, peers, and teams
- Experience working and influencing in a cross functional, matrix environment
- Proven ability to manage a broad variety of projects and priorities
- Experienced in problem solving and issue resolution
- High degree of communication and influencing skills
Preferred qualifications:
If you have the following characteristics, it would be a plus:- Master’s Degree in Global Health or a scientific or related discipline
- Risk Management experience
- Experience and knowledge of drug discovery and/or supply chain processes
- LI-GSK
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).
Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.
As an Equal Opportunity Employer, we are open to all talent. In the US, we also adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to neurodiversity, race/ethnicity, colour, national origin, religion, gender, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class*(*US only).
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.
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on Ukdiversity.recruitment@gsk.com or 0808 234 4391.
Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a UK Recruitment FAQ guide. Click the link and scroll to the Careers Section where you will find answers to multiple questions we receive .
As you apply, we will ask you to share some personal information which is entirely voluntary. We want to have an opportunity to consider a diverse pool of qualified candidates and this information will assist us in meeting that objective and in understanding how well we are doing against our inclusion and diversity ambitions. We would really appreciate it if you could take a few moments to complete it. Rest assured, Hiring Managers do not have access to this information and we will treat your information confidentially.
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Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit GSK’s Transparency Reporting For the Record site.
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