In this role, you will provide strategic administrative and operational support to senior leadership within Integrated Biologics Platform (Operations). As a trusted partner in a fast-paced global environment, you will proactively manage priorities, stakeholders, and planning.
Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources
Onboard Infection Prevention Control System Committee Operations • Responsible for professional and effective Cross-functional IPCS Committee operations, required meeting preparations, Minutes of the Meetings, reporting this duty directly to Captain onboard who is the Chair of the
The eTMF Specialist, Regulatory Affairs is responsible for the maintenance, quality, and inspection readiness of the electronic Trial Master File (eTMF) documents owned by Regulatory Affairs. The role ensures eTMF-relevant regulatory documentation is complete, accurate, timely, and
At EY you have the chance to build a career that is as unique as you are, with our global scale, inclusive culture and technology to become the best version of yourself. We’re counting on your voice
Blockstream was founded in 2014 by Dr. Adam Back and a group of fellow cryptographers and engineers passionate about Bitcoin and its potential to change the future of finance. We have become a market leader in
CTC are specialised industry experts who can help companies source the best talent and provide reliable HR and consulting services, support varied candidates in finding promising career opportunities and offer the latest in skill development training
Are you passionate about quality, precision, and working in a GMP‑regulated environment? We are currently seeking a detail‑oriented GMP Documentation Specialist (m/w/d) to join our client’s Manufacturing Operations team in a dynamic, fast‑paced biopharmaceutical environment. The
Specialist, ESG Reporting Location: Zurich, CH, 8005 At Barry Callebaut, we are on a journey to transform the cocoa and chocolate industry. As the world’s leading manufacturer of high-quality chocolate and cocoa products, our actions truly
Main Responsibilities: Maintain Regulatory Affairs content within the eTMF in accordance with regulatory requirements, ICH guidelines, and internal SOPs. Liaise closely with third parties to obtain regulatory eTMF documents. Prepare and perform ongoing quality control (QC) of regulatory
The Batch Record Reviewer supports clinical biologics manufacturing by performing operational review of executed batch records and ensuring documentation meets ALCOA+ , GDP , and GMP expectations. As part of the Manufacturing Operational Excellence team, this
Applications Manager The Applications Manager is responsible for ensuring continuity and guaranteeing the quality of the Applications, as well as managing the Application system maintenance activities, which include: Ensuring the proper functioning of applications and that
The Procurement Support Analyst is responsible for the end‑to‑end creation, accuracy, and maintenance of procurement contracts within the company’s trading and ERP systems. This role ensures that all commercial terms, pricing components, materials, vendors, and compliance
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our
The GMP Documentation Specialist supports clinical biologics manufacturing by performing operational review of executed batch records and ensuring documentation supports ALCOA+ standards and GMP expectations. The role is part of the Operational Excellence team within Manufacturing