Senior Director, Global Regulatory Lead - Siena

Site Name: Belgium-Wavre, Italy - Siena, Rockville Biopharm, USA - Pennsylvania - Upper Providence · Posted Date: Mar 6 2026 · Business Introduction · At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decad ...

A biotech company is looking for a highly motivated and qualified Regulatory Affairs Specialist who will report to the Regulatory Affairs Manager. · ...

A biotech company is looking for a Senior Regulatory Affairs Specialist to provide support in formulating and implementing regulatory strategies for product development. · Lead activities concerned with submission and approval of products to government agencies. · Develop content ...

You will lead global Chemistry, Manufacturing and Controls (CMC) regulatory strategy for complex biological products. · ...

Lead a global labelling team for oncology products and engage with key stakeholders to ensure effective development of GSK oncology labels. · ...

· As a therapeutic head within Labelling Strategy and Governance, you will lead a global labelling team for oncology products. You will engage with key stakeholders across R&D to ensure effective development of GSK oncology labels.You will shape labelling that is clear, complian ...

Site Name: Belgium-Wavre, Bangalore, GSK HQ, Siena, Stevenage, Warsaw · Posted Date: Feb · Business Introduction · At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering a ...

A biotech company seeks a highly motivated MEDICAL ADVISOR for clinical trials in oncology and rheumatology. · ...

+Job summary · We are seeking a highly motivated and collaborative Medical Doctor to join as Deputy Chief Medical Officer.You will play a key role in providing medical oversight, expertise and leadership to ensure the strategy, development and implementation of clinical trials,Re ...

A highly motivated and qualified MEDICAL ADVISOR is needed to support the management and development of clinical trials in oncology and rheumatology at Philogen S.p.A. · ...

The Quality Control Release & Stability Testing Director is accountable for end‑to‑end oversight of QC release and stability testing activities for clinical products.This leader will define strategy, build and lead high‑performing teams, drive technical and regulatory excellence, ...

Philogen S.p.A., a biotech company listed on the Milan Stock Exchange, seeks a Regulatory Affairs Specialist for their Clinical Department. · ...

The Vaccines Clinical Sciences Cluster Head is responsible for ensuring the delivery of robust clinical development plans for vaccines. · Accountable for clinical development planning of assets within their disease area. · Lead interpretation and critical evaluation of study resu ...

The Vaccines Clinical Sciences Cluster Head is responsible for ensuring the delivery of robust CDPs that explore new areas of interest and alternative development pathways. · Clinical Development: Accountable for clinical development planning of assets within their disease area. ...

Site Name: · Belgium-Wavre, Bangalore, GSK HQ, Siena, Stevenage, Warsaw · Posted Date: · Feb · Business Introduction · At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discoveri ...

This role offers a hybrid working model with a mix of on-site and remote work. Provides quality leadership for network strategy projects that strengthen our supply network. · ...

We're seeking a Head of Translational Research to advance our vaccine research and development efforts. You will lead a team of experts to translate scientific discoveries into impactful vaccine solutions. · Lead, coach and mentor a global team of approximately 15 experienced sci ...

We are looking for a highly motivated and qualified Senior Regulatory Affairs Specialist who will report to the Regulatory Affairs Manager and provide support in formulating and implementing regulatory strategies. · A contract and salary proportional to the experience of the succ ...

This role combines end-to-end process architecture change leadership data and AI-enabled insights inspection readiness and cross-functional governance to deliver consistent compliant measurable outcomes. · The GMASE Global Process Owner (GPO) owns a network of processes SOP(s) to ...

We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme. · W ...