Latest Business Insights Manager Jobs

Executive Director, External Strategy & Science Advocacy

This role involves leading the external engagement and policy advocacy for GSK's Development Sciences, working closely with regulatory agencies, industry consortia, and academic institutions to shape the future of pharmaceutical innovation. Key responsibilities include developing policy strategies, representing the organization in external forums, and advancing technical capabilities in clinical development and data science.

GSK

On-site Permanent

VIDRU Business Programs Strategy Director

The VIDRU Business Programs Strategy Director role involves translating the vision and priorities of the Vaccines and Infectious Diseases Research Unit into coherent, enterprise-wide programs. Key responsibilities include strategic planning, cross-functional collaboration, and ensuring the delivery of measurable business value through data-driven insights and effective governance.

GSK United States

Hybrid Permanent

Quality Oversight and Compliance Director

The Quality Oversight and Compliance Director at Pfizer will be responsible for developing and maintaining quality plans, ensuring inspection and audit readiness, and providing oversight of process deviations and investigations. This role involves interpreting and applying global regulations, driving compliance, and collaborating with stakeholders to identify and mitigate risks, ensuring the quality and integrity of Pfizer's medicines and vaccines.

Pfizer United Kingdom

On-site Permanent

Quality Oversight and Compliance Director

The Quality Oversight and Compliance Director will lead the development and maintenance of Quality Plans, ensure inspection and audit readiness, and provide quality oversight of process deviations and investigations. This role involves interpreting and applying regulatory requirements, identifying and mitigating compliance gaps, and driving continuous improvement in pan-regulatory processes and data quality.

Pfizer London, SW7 2AP, United Kingdom

On-site Permanent

Director, Digital Medicine: Respiratory, Immunology & Inflammation Research Unit

This role involves leading the development and implementation of digital medicine strategies to support clinical programs and studies in respiratory, immunology, and inflammation. You will work across various teams to design and validate digital biomarkers, enhance clinical trials with AI, and collaborate with external partners to accelerate capability and delivery.

GSK London, United Kingdom

On-site Permanent

Director, QC Systems

This role involves leading a global matrix programme team to transform incoming material testing and data management across GSK's manufacturing sites. Responsibilities include defining future-state operating models, creating global standards, partnering with ERP and LES teams, and ensuring data integrity and regulatory compliance.

GSK United Kingdom

Hybrid Permanent

Regional EM Engineering Lead

This role involves ensuring strong engineering performance at Contract Manufacturing Organization (CMO) sites, focusing on Large Molecule Drug Substance. Responsibilities include site assessments, capital project management, and engineering support for new product introductions and existing GSK products.

GSK United States

On-site Permanent

Regional EM Engineering Lead

This role involves ensuring strong engineering performance at Contract Manufacturing Organization (CMO) sites, supporting new product introductions, and managing engineering programs for Large Molecule Drug Substance. The position requires expertise in engineering aspects of large molecule drug substance and involves site assessments, capital management, and troubleshooting.

GSK

On-site Permanent

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMOs, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK Irvine, Alba / Scotland, KA12 8EL, United Kingdom

Hybrid Permanent

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK

Hybrid Permanent

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK

Hybrid Permanent

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMOs, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK

Hybrid Permanent

Senior Director, Head of Global Medical Governance, ViiV Healthcare

This role involves leading the global medical governance system at ViiV Healthcare, ensuring compliance and ethical standards across all medical activities. Responsibilities include developing and maintaining governance policies, advocating for medical governance, and collaborating with regional teams to embed best practices.

GSK United Kingdom

On-site Permanent

Senior Director, Head of Global Medical Governance, ViiV Healthcare

This role involves leading the global medical governance system at ViiV Healthcare, ensuring ethical and compliant medical practices across the organization. Responsibilities include developing and maintaining governance policies, advocating for medical governance, and collaborating with regional and local teams to embed robust practices.

GSK

On-site Permanent

Director, CMC Regulatory Affairs

Leads global CMC regulatory strategy for small molecule medicines, working across R&D, supply, quality, and commercial functions to ensure regulatory compliance and uninterrupted patient supply. Provides strategic direction on regulatory submissions, mentors regulatory staff, and engages with global authorities. Focuses on solving complex regulatory challenges while aligning with business objectives and patient impact.

GSK

Hybrid Permanent