Jobs in Reading

Global Medical Affairs Director, Autoimmune Diseases

The Global Medical Affairs Director leads strategic and operational programs for autoimmune diseases, focusing on innovative evidence, launch readiness, and post-market solutions. They develop and execute medical/scientific engagement strategies, provide expert input on clinical trials, and collaborate with internal and external stakeholders to maximize the value of Novartis medicines.

Novartis London, United Kingdom

Hybrid Permanent

Global Medical Affairs Director, Autoimmune Diseases

The Global Medical Affairs Director is responsible for developing and implementing strategic and operational programs for autoimmune diseases, focusing on innovative evidence, launch readiness, and post-market solutions. They lead medical-scientific input, evidence generation, and stakeholder engagement to maximize the value of new medicines and support global medical affairs initiatives.

Novartis

Hybrid Permanent

SME - MSAT EM Technical Operations DS/DP

This role involves collaborating with internal and external stakeholders to support the commercial manufacture of large molecule drug substances and sterile drug products. Responsibilities include executing technical strategies, managing product lifecycle activities, and ensuring compliance with GMP standards. The role also involves supporting CMOs in audits, technical transfers, and continuous improvement initiatives.

GSK

On-site Permanent

Senior SME - MSAT EM Tech Ops DS DP

This role involves leading technical operations and providing strategic support for the commercial manufacture of large molecule drug substances and sterile drug products. Responsibilities include executing technical strategies, collaborating with external manufacturing partners, and ensuring compliance with GMP standards and continuous improvement initiatives.

GSK United States

On-site Permanent

Associate Director, CMC Regulatory Science, International

This role involves developing and implementing CMC regulatory strategies for global submissions, providing guidance on regulatory CMC aspects, and ensuring compliance with health authority guidelines. The candidate will support multiple programs in various therapeutic areas, including vaccines, oncology, and rare diseases, and work closely with manufacturing and quality teams.

Moderna London, United Kingdom

On-site Permanent

Associate Director, CMC Regulatory Affairs, International

This role involves developing and implementing CMC regulatory strategies for international submissions, providing guidance on regulatory CMC aspects, and leading discussions with health authorities. The candidate will also support the creation of CMC submission templates and offer interpretations of regulatory guidance documents, ensuring compliance and efficient delivery of high-quality regulatory documentation.

Moderna London, United Kingdom

On-site Permanent

Vice President, Medical Affairs

As Vice President, Medical Affairs, you will lead the development and execution of integrated medical strategies for Recursion's clinical portfolio, focusing on areas like oncology, rare diseases, and immunology. You will collaborate with cross-functional teams to build evidence, engage key stakeholders, and ensure the translation of scientific insights into meaningful patient impact.

Recursion North Tyneside, NE29 8EP, United Kingdom

On-site 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

Quality and Regulatory Labelling Program Manager

This role involves leading global labelling initiatives to ensure compliance with regulatory standards across multiple markets. The Program Manager will work closely with cross-functional teams to manage change controls, mitigate risks, and drive continuous improvement in labelling processes.

Randstad Engineering Popley, Hampshire, RG24 9TW, United Kingdom £27 ph

Hybrid Contract

Director, QA Manufacturing

This role involves leading and developing the Front Line QA function at Seqirus Liverpool, ensuring pharmaceutical quality across all products. Responsibilities include providing 24/7 QA coverage, overseeing batch review and IT systems, and ensuring compliance with regulatory requirements. The role holder may also act as a QP, certifying and releasing products to market.

CSL United Kingdom

On-site Permanent

GLP/GCLP Vendor Oversight and QA Lead (EU)

This role involves leading the quality oversight of external partners in R&D and regulated activities, managing the vendor lifecycle from due diligence to continuous improvement, and ensuring compliance with GLP/GCP/GMP/GVP standards. The position requires close collaboration with various departments to maintain high-quality standards and regulatory compliance.

CSL United Kingdom

On-site Permanent

Clinical Study Administrator

As a Clinical Study Administrator, you will coordinate and manage the administrative aspects of clinical trials, ensuring that all documentation, regulatory submissions, and stakeholder communications are accurate and timely. You will work closely with various teams to maintain inspection readiness and support the smooth operation of multi-site studies.

AstraZeneca Chatham, ME4 4NP, United Kingdom

On-site Permanent

Senior Scientist New Modalities, Analytical

This role involves defining and delivering analytical strategies for new modality medicines, such as peptides and oligonucleotides, from early development to commercial launch. You will work closely with cross-functional teams to ensure robust quality control, regulatory compliance, and efficient commercial supply, while leveraging digital tools and AI to enhance decision-making and process robustness.

AstraZeneca Macclesfield, United Kingdom

On-site Permanent

Global Studies Asset Manager (GSAM)

The Global Asset Study Manager (GASM) at Roche/Genentech is responsible for the efficient execution of global clinical trials, ensuring consistency and compliance with IHC-GCP and Roche processes. Key responsibilities include coordinating study management, developing essential documents, driving innovation, and maintaining inspection readiness.

Roche Welwyn Hatfield, United Kingdom

On-site Permanent