Latest Healthcare Jobs

VP, Medicine Development Leader - Respiratory

Leads global development of a respiratory medicine from clinical proof of concept through approval, serving as the primary accountable leader across a cross-functional matrix team. Defines strategic vision, drives evidence generation, lifecycle planning, and regulatory strategy while coordinating input from R&D, manufacturing, commercial, and regulatory stakeholders to deliver patient-focused therapies.

GSK US$309,750 – US$516,250 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Works across cross-functional teams to ensure compliance, support inspections, and maintain product supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions in a complex, global environment.

GSK United States US$144,375 – US$240,625 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Lead CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Work cross-functionally to ensure compliance, support inspections, and maintain product supply. Influence regulatory decisions and mentor teams within a complex, matrixed environment.

GSK £144,375 – £240,625 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Works across cross-functional teams to ensure compliance, support inspections, and maintain product supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions in a complex, global environment.

GSK £144,375 – £240,625 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and ensuring compliance with global regulations. Works cross-functionally to address complex CMC issues, support inspections, and influence regulatory decisions. Focuses on maintaining product supply and optimizing regulatory processes across international markets.

GSK £144,375 – £240,625 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, ensuring compliance with global regulations and supporting submissions, inspections, and supply continuity. Works cross-functionally to shape regulatory approaches and mentor teams, with a focus on innovation and risk mitigation in complex regulatory environments.

GSK €90,000 – €150,000 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Works cross-functionally to ensure compliance, support inspections, and maintain product supply. Focuses on shaping regulatory approaches and mentoring teams in a complex, science-driven environment.

GSK €90,000 – €150,000 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Works cross-functionally to ensure compliance, support inspections, and maintain product supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions across complex international environments.

GSK £144,375 – £240,625 pa

Hybrid Permanent

SERM Scientific Director

The SERM Scientific Director will lead the safety evaluation and risk management of GSK's key assets, ensuring scientifically sound review and interpretation of data. They will develop and execute safety strategies, manage safety governance, and represent GSK on cross-functional teams to address product safety issues and improve regulatory adherence.

GSK

On-site Permanent

SERM Medical Director

The SERM Medical Director at GSK leads the safety evaluation and risk management of oncology assets in clinical development. Key responsibilities include interpreting safety data, managing safety signals, and providing expert medical input to support benefit-risk decisions. This role involves leading cross-functional teams, collaborating with regulatory authorities, and shaping the safety strategy for innovative oncology medicines.

GSK

On-site Permanent

(Fixed-Term) Manufacturing Associate, Drug Substance - Shift Position

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology, with a diverse pipeline of development programs across various diseases.As an employee, you'll be part of a continually growing organization,...

Moderna

(Fixed-Term) Manufacturing Associate II - Shift Position

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases.As an employee, you'll be part of a continually growing organization...

Moderna

Senior Manager - Engineering & Maintenance

The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is establishing a leading research, development, and manufacturing facility at...

Moderna

Senior Manager - CMC Regulatory Affairs Biopharm Development Projects

This role involves leading CMC regulatory activities for GSK's investigational, late development, and early commercial products. Responsibilities include driving CMC strategy, preparing regulatory documents, managing project activities, mentoring staff, and engaging with external agencies to ensure compliance and expedite submissions.

GSK Canterbury, United Kingdom

On-site Permanent

Senior Manager - CMC Regulatory Affairs Biopharm Development Projects

This role involves leading CMC regulatory activities for GSK's investigational, late development, and early commercial products. Responsibilities include driving CMC strategy, preparing regulatory documents, managing project activities, and mentoring staff. The position requires a strong understanding of regulatory requirements and the ability to communicate complex issues across departments and with external agencies.

GSK

On-site Permanent