Latest Managed Services Jobs

Regional Regulatory Manager

The Regional Regulatory Manager leads the development and execution of regional regulatory strategies for assigned assets, ensuring alignment with global strategies and regional requirements. This role involves close collaboration with global and local teams, providing regulatory expertise, managing submissions and approvals, and driving continuous improvement and innovation.

GSK

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 Engineering Technician (Secondment)

As a Senior Engineering Technician, you will provide comprehensive engineering support for the Sterile Value Stream, ensuring all production processes meet business and regulatory requirements. You will lead and supervise the Engineering Technician team, manage equipment breakdowns, and drive continuous improvement initiatives in a shift-based environment.

GSK Barnard Castle, United Kingdom

On-site Contract Shift-work

Audit Senior Lead (EMEA GMP Audit)

This role involves performing and managing GMP and compliance audits of Biopharm, Vaccines, and Pharmaceutical facilities. You will evaluate compliance with GMP, policies, and regulatory requirements, and provide subject matter expertise on sterile manufacturing. The role requires strong communication and influencing skills, and involves travel to various sites across the network.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent

Audit Senior Lead (EMEA GMP Audit)

This role involves performing and managing GMP and compliance audits of GSK's Biopharm, Vaccines, and Pharmaceutical facilities across the EMEA region. You will evaluate compliance with GMP, regulatory requirements, and quality management systems, and provide subject matter expertise in sterile manufacturing. The role requires strong communication and influencing skills to engage with senior stakeholders and produce clear audit reports.

GSK Worthing, United Kingdom

Hybrid Permanent

Audit Senior Lead (EMEA GMP Audit)

The Audit Senior Lead role involves performing and managing GMP and compliance audits of GSK's Biopharm, Vaccines, and Pharmaceutical facilities. Responsibilities include evaluating compliance, conducting various types of audits, and producing clear audit reports to inform senior management of risks and corrective actions.

GSK Barnard Castle, United Kingdom

Hybrid Permanent

Scientist, Analytical Operations - Small Molecule Stability Data Management

This role involves managing and improving stability data for small molecule studies, creating and maintaining study protocols, and producing clear data visualizations for regulatory submissions. You will work closely with cross-functional teams and external partners to drive process improvements and ensure data integrity.

GSK Stevenage, United Kingdom

Hybrid Permanent

Scientist, Analytical Operations - Small Molecule Stability Data Management

In this role, you will manage and improve stability data for small molecule studies, create and maintain study protocols, collect and analyse datasets, and produce clear summaries and visualisations for regulatory submissions. You will also support audits, collaborate with cross-functional teams, and drive process improvements through digital tool adoption.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent

Project Specialist (External Manufacturing-Drug Product)

This role involves managing technology transfer projects for external contract manufacturing organizations (CMOs) in the pharmaceutical sector, ensuring alignment between GSK and suppliers on timelines, quality, and technical deliverables. The specialist will coordinate cross-functionally across procurement, quality, technical, and supply teams to operationalize new assets or suppliers, with a focus on sterile drug products like monoclonal antibodies and vaccines. Key responsibilities include maintaining critical path schedules, mitigating risks, and driving project governance from transfer through to product launch.

GSK Worthing, United Kingdom €69,600 – €116,000 pa

Hybrid Permanent

Project Specialist (External Manufacturing-Drug Product)

This role involves managing technology transfer projects for external contract manufacturing organizations in the pharmaceutical sector, ensuring alignment between GSK and suppliers. The specialist will oversee project schedules, mitigate risks, and ensure timely delivery of drug products across critical assets like monoclonal antibodies, vaccines, and small molecules. Collaboration with cross-functional teams and supplier relationship management are central to driving successful operationalization within budget and timeline.

GSK East Hertfordshire, United Kingdom €69,600 – €116,000 pa

Hybrid Permanent

Project Specialist (External Manufacturing-Drug Product)

This role involves managing technology transfer projects for external drug product manufacturing with Contract Manufacturing Organisations (CMOs). The specialist will coordinate cross-functionally across Procurement, Quality, Technical, and Supply teams to establish and maintain project schedules, mitigate risks, and ensure timely delivery of assets within budget. The position emphasizes strong stakeholder engagement, governance, and retention of manufacturing knowledge across the supply network.

GSK Durham, DH1 3NG, United Kingdom €69,600 – €116,000 pa

Hybrid Permanent

Audit Senior Lead (EMEA GMP Audit)

The Audit Senior Lead role involves performing and managing GMP and compliance audits of biopharmaceutical, vaccine, and pharmaceutical facilities across the EMEA region. Key responsibilities include evaluating compliance, managing stakeholder engagement, and producing clear audit reports to mitigate risks and ensure regulatory adherence.

GSK

On-site Permanent

Audit Senior Lead (EMEA GMP Audit)

This role involves performing and managing GMP and compliance audits of biopharmaceutical, vaccine, and pharmaceutical facilities across the GSK Global Supply Chain. You will evaluate compliance with regulatory requirements and provide sterile manufacturing expertise, engaging with senior stakeholders and producing clear audit reports.

GSK

Hybrid Permanent

Audit Senior Lead (EMEA GMP Audit)

The Audit Senior Lead role involves performing and managing GMP and compliance audits of biopharm, vaccines, and pharmaceutical facilities. Responsibilities include evaluating compliance, managing stakeholder engagement, and producing clear audit reports. The role requires strong communication skills and subject matter expertise in sterile manufacturing.

GSK

On-site Permanent

Audit Senior Lead (EMEA GMP Audit)

This role involves performing and managing GMP and compliance audits of GSK's Biopharm, Vaccines, and Pharmaceutical facilities across EMEA and other highly regulated markets. Responsibilities include evaluating compliance, conducting various types of audits, and producing clear audit reports to inform senior management of identified risks and corrective actions.

GSK

Hybrid Permanent