document manager Jobs in Basel

To drive our continuous organic growth, we are constantly looking for highly qualified professionals. To strengthen our PM team we are looking for an experienced Analytical Project Manager QC (a) 100% who, by knowledge and character, suits our highly motivated and dynamic team. We are seeking someone who not only complements our team capabilities but also...

Johnson Johnson is seeking a Manager, Regulatory Medical Writing in Immunology at Allschwil, Switzerland. You will lead a team to prepare and finalize clinical documents while maintaining strategic direction and regulatory compliance.The role requires strong cross-functional collaboration, a detailed understanding of ICH guidelines, and hands-on mentorship...

Bachem Holding AG in Bubendorf is seeking a dedicated Manager QA Projects (a), 100% to strengthen the Quality Assurance team. You will represent QA in product-related projects at the Bubendorf site and ensure cGMP compliance across Production, QC and Project Management.Responsibilities include defining control and lifecycle strategies from development...

Johnson & Johnson is seeking a Manager, Global Labeling Product Leader to be based in Allschwil, Switzerland, or nearby Swiss locations. You will lead the development and governance of primary and derived labeling documents for assigned compounds, ensuring global regulatory compliance and high-quality labeling deliverables.You will coordinate...

Johnson & Johnson is seeking a Manager, Global Labeling Product Leader to base in Allschwil, Switzerland, Berne, or Zug. You will lead labeling documents (CCDS, USPI, EU Product Information) and derived labeling, ensuring quality, compliance, and strategic alignment across regions.You will guide timelines, coordinate across regulatory affairs, clinical, and...

pClinilabs, LLC. seeks a Senior Proposal Manager to lead the end-to-end development, review, and submission of client proposals and budgets for CRO, CRU, and Corelab services. /ppYou will coordinate cross-functional teams across BD, Operations, Finance, Legal, and Contracts to ensure compliant, competitive documents that meet sponsor requirements. The role...

VIATRIS INNOVATION GMBHViatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands, combining the best of both to more holistically address healthcare needs globally. With a mission to empower people worldwide to live healthier at every stage of life, we provide access at scale, currently supplying...

At Endress+Hauser, progress happens by working together. As the global leader in measurement instrumentation, with over 18,000 employees, we shape the future in the field of process automation. Whether developing and realizing new technology as a team, collaborating to build instrumentation, or strengthening vital relationships with countless global...

h3VIATRIS INNOVATION GMBH /h3pViatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands, combining the best of both to more holistically address healthcare needs globally. With a mission to empower people worldwide to live healthier at every stage of life, we provide access at scale, currently...

ppDescription /p h3JOB SUMMARY /h3 pThe Study Start-up Lead (SSUL) reports to the Global Feasibility, Regulatory and Start-up Head and is responsible for leading and overseeing the full lifecycle of regulatory submissions for clinical trials conducted globally or regionally till last participant site is activated, ensuring startup deliverables and timelines...

h3About this position /h3pAs the Senior Documentation Specialist, you ensure the effective management, quality, completeness, and inspection readiness of essential clinical trial documentation for assigned studies, programmes or documentation activities, including the sponsor TMF and oversight of CRO and laboratory TMFs. You acts as an experienced TMF...

Job ID: 41975 | Location: Pratteln, Canton of Basel-Landschaft, Switzerland | Work Model: Hybrid As Head of ESHA & IGSM, you will own and drive Clariant's integrated Environment, Safety, Health & Affairs (ESHA) and Integrated Global Standards Management (IGSM) strategy covering a network of approximately 70 production sites worldwide. Reporting directly to...

To drive our continuous organic growth, we are constantly looking for highly qualified professionals. To strengthen our team in the Global Engineering department, we are looking for a dedicated Senior Commissioning & Qualification (C&Q) Lead (f/m/d), 100%. In this role, you are responsible for the strategic planning, execution, and oversight of...

Introduction Move the world with us! AIT is a global freight forwarding company that has offices all around the world. Are you looking for a fast-paced, exciting and dynamic job? Then you are a perfect fit for our company! Join our team, be part of the international supply chain and move the world with us! If that sounds interesting, then make AIT...

ppWe are an internationally leading Swiss traditional brand for bathroom fittings and high-quality fixtures. Our products and services stand for quality, innovation and design in the bathroom, in public facilities and in the kitchen. We owe our success to the commitment and daily efforts of our motivated and globally active employees. Would you like to...

pJoin HALBA as a Project Manager in Engineering, where quality and sustainability are core values. Enjoy a supportive work environment with great benefits! /ph3Tasks /h3ulliOversee investment projects from planning to implementation, managing budgets. /liliCreate and coordinate 2D and 3D layouts for production areas and machinery. /liliHandle technical...

DescriptionJOB SUMMARYThe Senior Director of Business Development is responsible for developing and maintaining relationships between Clinilabs and pharmaceutical/biotechnology/device company clients. Relationships are developed and maintained by the following:(a) calling on clients and prospective clients on a regular basis,(b) engaging in direct, virtual...

DescriptionJOB SUMMARYThe Senior Director of Business Development is responsible for developing and maintaining relationships between Clinilabs and pharmaceutical/biotechnology/device company clients. Relationships are developed and maintained by the following:(a) calling on clients and prospective clients on a regular basis,(b) engaging in direct, virtual...

ph3Overview /h3pMonte Rosa Therapeutics is seeking a highly skilled and self-motivated regulatory professional to join our team as an Associate Director of CMC Regulatory Affairs. The CMC Regulatory Affairs will serve as a key regulatory strategist and author for the Chemistry, Manufacturing, and Controls components of Monte Rosa's global regulatory filings....

# Security GuardJet AviationBasel, BS, CH, 40308 days agoJob descriptionPosition SummaryAs a Security Guard at Jet Aviation, you will ensure the safety and protection of people, assets, and facilities while representing the company professionally. You will interact with employees, visitors, and customers, applying Jet Aviation’s values and vision. This...