Quality and Regulatory Work Engineer

RiverBank’s mission is to be the digital bank that makes financing to SMEs and Real Estate professionals easy. From our offices in Amsterdam, Paris and head-office in Luxemburg, we act as a niche lending specialist. Our core focus is to grant loans to Small and Medium Enterprises and Real Estate Investors in Europe using a fast, flexible and reliable IT...

Joining Davidson not only means joining a group of 3,000 consultants in 6 countries and 2 continents, but also joining a company that has been voted a Great Place To Work France and Europe by its employees for no less than 4 years, as well as one of the largest B Corps in France, named Best in the World in the employees" category in 2022! (B Corps" form a...

Joining Davidson not only means joining a group of 3,000 consultants in 6 countries and 2 continents, but also joining a company that has been voted a Great Place To Work France and Europe by its employees for no less than 4 years, as well as one of the largest B Corps in France, named Best in the World in the employees" category in 2022! (B Corps" form a...

bioMérieux S.A. **CDI- Regulatory Affairs Specialist F/M** A family-owned company, bioMérieux has grown to become **a world leader in the field of in vitro diagnostics**. For almost 60 years and across the world, we have imagined and developed **innovative diagnostics solutions** to **improve public health**. Today, our teams are spread across 45...

Description : Experience leading multiple sites and teams. Direct experience with compliance to the GLP regulations and ISO 17025 in a research laboratory. Oversite of the GLP master schedule and inspections. Leading and overseeing implementation of the eQMS application in EMEA. •Responsible for leading the Quality...

This hybrid role is based in Lyon , France, allowing you to split your time between working from home and our office in this culturally rich city. Proficiency in English is essential, ensuring effective communication within our diverse and collaborative work environment. This arrangement supports a balanced lifestyle and fosters productivity. With a...

**Company Description** At QIMA, we’re on a mission to help our clients make products consumers can trust. Working with over 30,000 global brands, retailers, manufacturers and food growers, we are on the ground wherever products are made. We help businesses secure every step of their supply chain with quality inspections, supplier audits, certifications,...

**WHO WE ARE** Infinity Global is the premier provider of branded packaging and product for the luxury segment, specializing in global sourcing and logístical solutions for premium retail and specialty brands. We believe in building intimate customer relationships by providing the highest level of service and quality to our customers. Our employees are...

**WHO WE ARE** Infinity Global is the premier provider of branded packaging and product for the luxury segment, specializing in global sourcing and logístical solutions for premium retail and specialty brands. We believe in building intimate customer relationships by providing the highest level of service and quality to our customers. Our employees are...

France **Position Description** - Do you recognize yourself as an engaged team player with great leadership skills? Are you looking for new challenges and growth by leading the technical transformation towards sustainable products? Are you ready to become a part of a management team responsible for delivering Propulsion systems?**Who are we?** We,...

Semarchy is looking for a FullStack Engineer with a passion to build great products using cutting-edge technologies and best engineering practices. **What you will do** - Collaborate with various team members and stakeholders on requirements definition and feature design & development - Work across the stack to deliver new features from start-to-finish -...

Master’s Degree - Operational experience - Proven track record of senior stakeholders engagement - Advanced excel and data analysis skills - Experience in program management, customer research and analytics, and/or customer experience/success - Fluent in French and English You want to develop yourself in a team that leads complex and business critical...

Job Summary: Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our Clinical Operations team. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous expertise and can...

Overview: Venn Life Sciences (part of the hVIVO Group) is an Integrated Drug Development partner offering a unique combination of drug development consultancy, clinical trial design expertise and biometry activities. Venn’s capabilities and expertise include: CMC, Non-Clinical, Clinical Development, Biometry and Regulatory Affairs. We have dedicated...

Overview of the role:Venn Life Sciences (part of the hVIVO Group) is an Integrated Drug Development partner offering a unique combination of drug development consultancy, clinical trial design expertise and biometry activities. Venn’s capabilities and expertise include: CMC, Non-Clinical, Clinical Development, Biometry and Regulatory Affairs. We have...

Semarchy is looking for a FullStack Engineer with a passion to build great products using cutting-edge technologies and best engineering practices. **What you will do** - Collaborate with various team members and stakeholders on requirements definition and feature design & development - Work across the stack to deliver new features from start-to-finish -...

Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We...

Venn Life Sciences (part of the hVIVO Group) is an Integrated Drug Development partner offering a unique combination of drug development consultancy, clinical trial design expertise and biometry activities. Venn’s capabilities and expertise include: CMC, Non-Clinical, Clinical Development, Biometry and Regulatory Affairs. We have dedicated operations in...

Overview , a business unit of RTI International, is an independent and internationally recognised research organisation. We provide healthcare consulting and research expertise to optimise decision making for pharmaceutical, biotechnology, and medical device products across the development and marketing lifecycle. Clients rely on our expertise, quality...

Job Summary: Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based in Lyon, Regulatory Submissions Manager to join our Clinical Operations team. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous expertise and...