Emplois actuels liés à Global C&q Director - Wavre - GSK
-
Director, Global Real-world Evidence
il y a 4 jours
Wavre, Belgique GSK Temps plein**Site Name**: USA - Pennsylvania - Upper Providence, Belgium-Wavre, UK - London - New Oxford Street **Posted Date**: Oct 10 2024 For drugs to be successful, there must be robust health outcomes data to support launch optimization, reimbursement and maintain market position. Specifically, evidence must be maintained throughout the product lifecycle as...
-
Executive Medical Director/SERM Head
il y a 5 jours
Wavre, Belgique WhatJobs Temps pleinExecutive Medical Director/SERM Head – Oncology Join to apply for the Executive Medical Director/SERM Head – Oncology role at GSK. Key Responsibilities Lead and inspire a global team of senior medical and scientific safety professionals. Define and drive the strategic direction and vision of clinical safety and pharmacovigilance activities in alignment...
-
Finance Director Belux
il y a 4 jours
Wavre, Belgique GSK Temps plein**Site Name**: Belgium-Wavre **Posted Date**: Dec 5 2024 **Job purpose**: The Finance Director BeLux provides finance business partnering and leadership to the Local Operating Company (LOC) and is accountable for legal and statutory compliance of the Pharma legal entity. As a member of the LOC Leadership Team, this role will provide support to the General...
-
Senior Manager, Procurement
il y a 4 jours
Wavre, Belgique GSK Temps plein**Site Name**: Belgium-Wavre **Posted Date**: Sep 12 2024 Job Purpose As the **Senior Manager, Head of Procurement **you will be at the forefront of driving GSK’s purpose to **unite science**, **technology**, and **talent** to get **ahead of disease** together. You will do so by partnering with Indirect spend owners across all GSK business lines, and...
-
Senior Manager, Procurement
il y a 4 jours
Wavre, Belgique GSK Temps plein**Site Name**: Belgium-Wavre **Posted Date**: Dec 6 2024 **Job Purpose**: As the **Senior Manager, Procurement - Capital Construction**, you will spearhead the development, execution, and management of comprehensive, integrated category strategies for Capital Investment. In this role, you will serve as the **Category Lead for all the Capital Projects in...
-
Sales & Growh Director (H/F/X)
il y a 1 semaine
Wavre, Belgique WhatJobs Temps pleinActeur européen de premier plan dans le domaine des services réglementaires notre client, basé en Belgique , accompagne un grand nombre d’entreprises internationales. L’entreprise, en pleine croissance, combine expertise scientifique, orientation client et ambition internationale. Forte d’un potentiel de croissance significatif, elle développe une...
-
Associate Director; Pharmacovigilance Agreements
il y a 4 jours
Wavre, Belgique GSK Temps plein**Site Name**: UK - London - New Oxford Street, Belgium-Wavre, USA - Pennsylvania - Upper Providence **Posted Date**: Sep 12 2024 As Associate Director, Pharmacovigilance Agreements & Safety Clauses (PVASC) you will support Pharmacovigilance Operations (PV Ops) in in alignment with GSK standards and regulatory timelines whilst driving the implementation of...
-
Associate Director, Gra Precision Medicine
il y a 4 jours
Wavre, Belgique GSK Temps plein**Site Name**: UK - London - New Oxford Street, Belgium-Wavre, Poznan Grunwaldzka, Switzerland - Zug, UK - Hertfordshire - Stevenage **Posted Date**: Jan 30 2025 We are seeking an Associate Director, Global Regulatory Affairs (GRA) Precision Medicine & Digital Health to ensure the development and execution of Precision Medicine and Digital Health regulatory...
-
Senior Director, Quality Operations Vaccines
il y a 4 jours
Wavre, Belgique GlaxoSmithKline Temps plein**Senior Director, Quality Operations Vaccines**: **The posting period will end on the 15th of February in 2026**: **The role can be done from any location that is close to a GSK location**: **Business Introduction**: We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance. Our network of 37...
-
Director, Senior Counsel R&d Legal Operations
il y a 4 jours
Wavre, Belgique GSK Temps plein**Site Name**: Belgium-Wavre, UK - London - New Oxford Street **Posted Date**: Oct 10 2024 ***Senior Counsel R&D Legal Operations**:** Location****: - Belgium (Wavre) or UK (New Oxford Street, Central London)** This Senior Counsel position is critical to support the Vaccines Research & Development and the Vaccines Medical organizations. The role is...
Global C&q Director
il y a 2 heures
**Site Name**: GSK HQ, Belgium-Wavre, Upper Merion, Zebulon
**Posted Date**: Nov 7 2025
**Global C&Q Director**:
**Business Introduction**
**GSK remains committed to achieving bold commercial ambitions for the future. By 2031, we aim to deliver £40 billion in annual sales, leveraging our existing strong performance momentum to significantly increase our positive impact on the health of billions of patients globally. Our Ahead Together strategy is centred on early intervention to prevent and alter the course of disease, thereby protecting people and supporting healthcare systems.**
**Our diverse portfolio consists of vaccines, specialty medicines, and general medicines.**
**Through continuous innovation and a dedicated focus on scientific and technical excellence, we strive to develop and launch new, groundbreaking treatments that address critical health challenges.**
**Position Summary**
**The Global C&Q Director will lead and manage the consistent deployment of best in class capability and capacity of commissioning and qualification activities within the project portfolio under the accountability of Global Capital Projects group (GCP). This role is responsible for ensuring that all project equipment, systems, and processes consistently meet regulatory and company standards to ensure product quality and patient safety. The Global C&Q Director will work closely with cross-functional teams, including engineering, quality assurance, manufacturing, and regulatory affairs, to ensure the delivery of compliant and efficient commissioning and qualification programs. They will work to establish strong partnerships for efficient deployment of C&Q capability and resources across all geographies**:
The Global C&Q Director will drive towards best in class practices leveraging digital and AI to continuously improve and drive superior performance within commissioning and qualification of large capital projects.
**Responsibilities**:
- **Leadership and Strategy**:
- Support the development and implement global C&Q strategies, policies, and procedures based on company standards and prevailing regulations.
- Collaborate with senior management to align C&Q activities with business objectives and regulatory requirements.
-**
Project Management**:
- Oversee the planning, execution, and completion of C&Q projects across multiple projects.
- Ensure projects are delivered on time, within budget, and in compliance with regulatory standards.
-**
Technical Expertise**:
- Provide technical guidance and support for C&Q activities, including risk assessments, protocol development, and execution.
-**
Quality and Compliance**:
- Ensure that all C&Q activities comply with GSK’s quality management system and applicable regulatory requirements (e.g., FDA, EMA, MHRA).
- Implement continuous improvement initiatives to enhance C&Q processes and outcomes.
-**
Team Development**:
- Support the recruitment, training, and mentoring of C&Q staff to build a high-performing global team.
- Conduct performance evaluations and provide feedback to support professional growth.
- Be a global team ambassador to the local site project environment.
- Act as a visible advocate for diversity in engineering and project delivery.
- Act as a visible advocate for GSK Safety Life Saving Rules.
-**
Stakeholder Management**:
- Build and maintain strong relationships with internal and external stakeholders, including suppliers, contractors, and regulatory agencies.
**Qualifications/Skills**:
**Basic Qualifications**:
- Engineering degree (Mechanical, Electrical, Chemical, Civil/Structural).
- Extensive project validation experience and proven experience in leading validation teams in pharmaceutical or biotech industry.
- Proven track record of successfully leading and managing global C&Q projects across all geographies and end-to-end.
- Proven track record of regulatory authority audit participation and defence of validation project plans and results.
- In-depth knowledge of regulatory requirements and industry standards (e.g., GMP, GAMP, ICH guidelines).
- Experience in biopharm specific unit operations and platforms - drug substance/primary, DP/sterile filling, and packaging.
- Strong project management skills, with experience in managing complex, multi-site projects.
- Deep and broad understanding of the capital project lifecycle - design, construction, commissioning, qualification, to operation.
- Strong stakeholder management and influencing capabilities
- Leadership skills that enable the introduction of new ways of working and accelerated change management.
- Must be able to interact well with peers, subordinates, and senior personnel in scientific, engineering, and operational disciplines.
- Demonstrated ability to participate as a leader or member on cross-functional and self-directed work teams.
- Must be comfortable and thrive in ambiguity and think strategically to solve complex problems.
**Preferred Qualifications**:
- Maste
