Ssu & Regulatory Specialist Ii

Description Site Start-Up & Regulatory Specialist II Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to...

Description Site Start-Up & Regulatory Specialist I Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help...

op Qualifications: Regulatory and Product Compliance background, Safety/RF knowledge in Information Technology Equipment (ITE), which means computer hardware Job Summary: As part of the Zebra Enterprise Visibility and Mobility (EVM) Regulatory department, this role is to provide Regulatory support for new product development as well as continued compliance...

**Summary**: Location: Montréal, #LI-Hybrid We are seeking an innovative, experienced, and agile Clinical Trial Associate (CTA) who is driven by accelerating the start-up of globally run clinical trials and who is motivated in making a difference in reimagining medicine. About the role: The CTA supports SSO Study Start-Up Manager and SSO Clinical Project...

100,000. That’s how many patients participate in our clinical trials at any given time. Global Clinical Operations (GCO) touches patients’ lives every day acting as a link between science and medicine. Envision the impact you could have! #GCO The Clinical Trial Associate (CTA) supports SSO Study Start-Up Manager and SSO Clinical Project Manager in...

The Quality and Regulatory Specialist is responsible for maintaining and managing the daily operations of the Patterson Quality Management System. Manages compliance activities with responsibility for results in terms of ongoing effectiveness of the QMS and of conformance to applicable regulation, standard and company policies. Supports activities related to...

REGULATORY REPORTING SPECIALIST (JOB NUMBER: FIN-110422-001-LJ) At BNP Paribas Canada, it is our employees which make the difference... Our 75 nationalities are part of our diversity! Do you like challenges, a structured framework, the prospect of optimizing and innovating? You are known for your originality and want a certain freedom to think while...

**See if you are our next**: **BILLINGUAL REGULATORY AFFAIRS SPECIALIST (Operating Room Experience Required)** Working at Vision Group's head office is working for the North American leader in vision correction. It means being able to concretely contribute to the development of the company and support more than 12 brands and more than 70 clinics across...

At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. The Program Coordinator II (PC II) coordinates projects of small, mid-size, within one or across multiple business units, in support of the...

700 generic products and 6 biosimilars covering 280 molecules and medicinal ingredients spanning multiple therapeutic areas represents the Sandoz portfolio of products in Canada. The Specialist Regulatory Affairs supports the increasing expansion of our product portfolio, and continuous improvement and compliance of our marketed products. Join us, in our...

**Regulatory Testing Specialist** **Job Description**: Compliance Testing Specialist is responsible for the administration and coordination of regulatory testing activities for foreign manufacturers in conjunction with local Dorel teams, and in compliance with DHP procedures and requirements. **Tasks, without being limited to, include**: - Coordinates...

**Certara is hiring a Quality Assurance Specialist to join our Integrated Drug Development team!** **At Certara, we accelerate medicines to patients by partnering with life science innovators.** - informed decision-making & reduced clinical trial burden - higher R&D productivity - improved patient outcomes & increased patient access to medicines -...

Description Clinical Research Associate II **Come discover what our 25,000+ employees already know**: work here matters everywhere. We’re a growing and evolving biopharmaceutical industry leader, which means you’ll have endless opportunities to work with experts around the world and build the career you’ve dreamed of. As a part of the Syneos Health...

Hi there! Thanks for stopping by Are you actively looking for a new opportunity? Or just checking the market? Wellyou might just be in the right place! Lightspeed is seeking a customer service oriented individual to provide full-time technical assistance for our popular Payment Systems.The Financial Support Specialist II will be counted on to provide...

Work Term: Permanent - Work Language: English - Hours: 38 to 44 hours per week - Education: Master's degree - Experience: 5 years or more - Bioengineering and biomedical engineering - Mechanical engineering **Tasks**: - Analyze and provide advice on the managerial methods and organization of an establishment - Develop quality management and quality...

Do you want to join an international team working to improve the future of healthcare? Do you want to improve the lives of millions of people? Grifols is a global healthcare company which, since its foundation in Barcelona in 1909, has been working to improve the health and well-being of people all over the world. Our four divisions - Bioscience, Diagnostic,...

Work Term: Permanent - Work Language: English - Hours: 42 to 44 hours per week - Education: Master's degree - Experience: 5 years or more **Tasks**: - Analyze and provide advice on the managerial methods and organization of an establishment - Conduct quality audits - Develop quality management and quality assurance standards - Conduct research to determine...

**JOB TITLE**:Clinical Research Associate (CRA) II **LOCATION**: Canada (Remote) **REPORTS TO**:Manager, Monitoring & Site Management **DEPARTMENT**: Monitoring & Site Management **JOB SUMMARY**: Performs and coordinates all aspects of the clinical site monitoring services, assessing for protocol and regulatory compliance. Responsibilities include...

Description de poste en anglais à suivre / English job description below Rédacteur(e) II - Sinistres Biens Entreprise Le rôle que jouent le rédacteur(e) sinistres Biens entreprise est fondamental au succès continu d’AIG et à la position de chef de file qu’occupe la Compagnie sur le marché de l’assurance. AIG continue d’ouvrir la voie en...

**Supervisor II, Environmental Monitoring** **Purpose of the Job**: Establishes and maintains Environmental Monitoring (EM) programs of Jubilant’ sites that meet the internal standards of Jubilant Pharma and those of the regulatory agencies (HPFBI, FDA, EU, etc.). **Key Accountabilities**: - Plans, schedules, and maintains all environmental monitoring...