Senior Director Quality Business Partner: Research & Precision Medicine

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Senior Director Quality Business Partner: Research & Precision Medicine

Sector: Audit, Research and Development
Role: Senior Executive
Contract Type: Permanent
Hours: Full Time
Site Name: UK - Hertfordshire - Stevenage, USA - Massachusetts - Cambridge, USA - Massachusetts - Waltham, USA - Pennsylvania - Upper Providence
Posted Date: Nov 27 2024

Are you energized by the opportunity to develop and deliver quality strategies for Research and Precision Medicine? If so, the Senior Director, Quality Business Partner: Research & Precision Medicine role could be an exciting opportunity to explore.

The Senior Director, Quality Business Partner: Research and Precision Medicine is responsible for developing and delivering the quality strategy for the portfolio within the scope of Research and Precision Medicine.

The incumbent manages a small team of Quality Business Partners and will provide assurance to GSK R&D senior management that GSK research and precision medicine processes are effective in ensuring the integrity of the data, compliance with internal GSK requirements and applicable external regulatory requirements and industry best practices.

The position will develop methods to effectively and efficiently provide proactive quality support and consultation and drive quality into the business.

The Senior Director, Quality Business Partner: Research and Precision Medicine is a member of the Function & Process Quality Leadership team and, with other members of the LT, is responsible for the strategy and direction of this function.

Responsibilities include

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

Functional Expertise:

• Has direct accountability for the quality strategy for Research and Precision Medicine.
• Considered a strong trusted partner for Research and PMed leaders.
• Build and lead a Quality team that provides experienced quality support for research and precision medicine assets and projects.
• Continually evaluate the strategic approach, drive changes in R&D QuRE processes and modify the quality strategy and plan to meet the changing needs of the organization, regulatory requirements and industry best practices.
• Identify and drive continuous quality improvements as a consequence of risk assessments, audits, inspections, trends/metrics and root cause analysis.
• Provide input into the global audit plan based on identified signals/trends/risks/gaps.
• Provide guidance and expectations to the business to build in quality by design and to enable the execution of external regulations and internal standards.
• Interact with executive management and cross-functional business partners to identify areas of greatest quality risks and obtain information and feedback relevant to improvement. Drive issue resolution.
• Ensure rapid communication of critical quality risks and issues, including potential misconduct to business partners and executive management.
• Support the preparation, execution and closeout of health authority inspections.
• Participate in Due Diligence and Merger & Acquisition activities in early phases of development or related to CDx/IVD.
• Provide training to QuRE and Business Partners regarding Good Research/Science Practices, GLP, clinical testing, IVD/CDx, and Medical Devices.

Leadership/People Management:

• Establish a network of peers in Big Pharma to enable constant benchmarking.
• Build and maintain a Research and Precision Medicine Quality team by creating an environment that attracts, develops and retains high-quality employees.
• Provide leadership, professional development, mentoring and coaching for direct and indirect reports, including talent planning and performance management.
• Develop, motivate, and empower direct reports to have a high degree of accountability for performance and the oversight of key deliverables.

Other:

• Lead multidisciplinary or cross-functional work/project teams.
• Provide guidance and expectations to the business to enable execution of external regulations and internal standards on a global and cross-functional level.
• May influence the external environment through interactions with regulators, trade associations, and professional societies.
• Liaise with stakeholders in R&D to understand global and local needs and determine priorities.

Why you?

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

• Bachelor's degree or equivalent in scientific, engineering or quality-related field.
• Experience in the pharmaceutical industry and/or quality assurance, quality management or risk management.
• Leadership of GCP/GVP/GLP Audit program management.
• Must have operated in a senior management role with extensive supervisory/management experience.
• Knowledge of GLP, GCP, Medical Device and IVD requirements, as well as analytical, organizational and planning skills.
• Knowledge of risk management and quality narratives.
• Budget and resourcing management experience.
• Experience leading global multidisciplinary, functional, line and matrix teams.
• Experience managing key stakeholders.

Preferred Qualifications:

If you have the following characteristics, it would be a plus:

• Experience in supporting regulatory authority inspections.
• Broad knowledge of Risk-based quality management, root cause analysis and quality by design concepts and methodology.
• Digital savviness, experience with AI/ML and data analytics.
• Ability to work effectively in an international multicultural matrix organization.
• Effective communication/negotiation skills and customer management skills.

Why 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 organization 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.

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