Drug regulatory Kanton Waadt Jobs

 ...innovation and excellence drives us to develop cutting-edge medical devices that positively impact patients' lives worldwide. Regulatory Affairs Manager Position Overview: For our site located in Le Mont-sur-Lausanne, we are seeking a highly skilled and motivated... 

Regen Lab SA based in Le Mont-sur-Lausanne. We are a Swiss leading medical device company comprised of a dynamic team dedicated to revolutionizing healthcare. Our commitment to innovation and excellence drives us to develop cutting-edge medical devices that positively ...

Entreprise : Notre client est une entreprise internationale spécialisée dans le développement de dispositifs médicaux. Description du poste : * Collaborer à la réalisation du design avec les départements Marketing, Affaires Réglementaires et R&D * Etablir les spécifications...

 ...Job Description: As a Regulatory Affairs Manager you will be responsible for ensuring compliance with regulatory requirements related to...  ...and submit regulatory submissions including Investigational New Drug (IND) New Drug Application (NDA) 510(k) PreMarket Approval (PMA... 

LHH Recruitment Solutions is a specialized talent recruitment boutique. We provide tailored services to help companies find the best candidates for their staffing needs. With deep industry expertise and a commitment to excellence, LHH RS is a trusted partner in Switzerland...

 ...of registrations, renewals and lifecycle management; Review and validate products’ artworks and marketing campaigns to ensure regulatory compliance; Write and review SOP, WKI, FORM for regulatory affairs-related processes; Manage non-conformity process in particular... 

 ...for a dynamic professional to step into a pivotal role that includes responsibility in Design Control Quality Assurance (QA) and Regulatory Affairs (RA) for one of our clients. KEY RESPONSIBILITIES Oversee Project Excellence Quality Assurance and Design Control:... 

 ...project aims to revolutionize the discovery of new anti-infective drugs and to advance our understanding of the mechanisms underlying...  ...and researchers to integrate findings into broader anti-infective drug discovery efforts. Collaborative projects will include screening... 

 ...For Use (IFU) for our medical devices, ensuring compliance with regulatory standards. Register medical devices in various regulatory...  ...the management of Instructions For Use for medical devices or drugs. Familiarity with the structure of technical documentation and... 

 ...recognized products. The new position of a Manager for Sterile Drug Product requires significant experience in manufacturing...  ...(FMEA) ~ Understanding of process engineering analytical and regulatory aspects of sterile drug product manufacturing Your solutionoriented... 

 ...packaging and testing activities associated with Small Molecules Drug substances, Drug Products and Primary Packaged Products. The...  ...partners and Incyte, Support Incyte and license partners regulatory submissions as well as product launches, Cooperate with the... 

 ...at a newly ramped up Manufacturing Site for Oral Solid Dosage Drugs and a Center of Excellence for projects and New Product Introductions...  .../reports. Conduct and assist others in industry and regulatory research including research into industry standards/FDA guidelines... 

 ...industry ~ Thorough understanding of cGMPs and Swiss EU and FDA regulatory requirements Your tasks: * This position is responsible...  ...validation Experience in Data Integrity Good understanding of the drug development process from discovery through to regulatory filing... 

 ...dedicated to empowering researchers in immunology, immuno-oncology, and neuroscience to push the boundaries of scientific discovery and drug development. We build solutions that simplify technology adoption of spatial biology to support the development of diagnostic tools... 

 ...dedicated to empowering researchers in immunology, immuno-oncology, and neuroscience to push the boundaries of scientific discovery and drug development. We build solutions that simplify technology adoption of spatial biology to support the development of diagnostic tools... 

 ...dedicated to empowering researchers in immunology, immuno-oncology, and neuroscience to push the boundaries of scientific discovery and drug development. We build solutions that simplify technology adoption of spatial biology to support the development of diagnostic tools... 

 ...dedicated to empowering researchers in immunology, immuno-oncology, and neuroscience to push the boundaries of scientific discovery and drug development. We build solutions that simplify technology adoption of spatial biology to support the development of diagnostic tools... 

 ...functional teams, provide legal guidance, and contribute to the success of our medical devices business. TASK & RESPONSIBILITIES Regulatory Compliance: Interpret and apply relevant Swiss and international regulations related to medical devices. Advise on quality... 

Overview: The QC Specialist is responsible for the QC Physico-Chemistry operational activities related to Drug Substance (DS), In-Process-Control (IPC) and Raw Materials (RM) testing & release at Incyte QC Bioplant. This includes (but is not limited to) the planification... 

 ...Job description Develop and execute validation protocols to ensure processes and instruments are compliant with regulatory standards. Oversee the commissioning and qualification of utilities (ex. purified water systems, clean steam systems, HVAC systems, and...]...