Trabajo de Regulatory Compliance Analyst en Ourense

AI Technical Business Analyst 2x per week in the Valencia office Our client, a IT consultancy is looking for a AI Technical Business Analyst to join the team on a permanent basis. You'll the link between business stakeholders, engineering teams for the internal AI tooling ecosystem. Responsibilities Work closely with stakeholders to , evaluate, and prioritise functional and non-functional...

A healthcare technology company based in Galicia, Spain is seeking a Regulatory Affairs Specialist to ensure compliance with medical device reporting requirements. Responsibilities include serving as the local contact with Spanish authorities, managing vigilance processes, and supporting audits. Candidates should have relevant experience in medical writing and complaint processing, along with a...

Description Our team is seeking an Environmental Compliance Manager who will support Spain Environmental Assurance and Protection (EAP) team across all business lines, and lead one business line within Spain. This role is responsible for ensuring strategy and operational tactics are executed by providing technical support for existing operations and future expansion across multiple facilities...

Nilorn Worldwide is a unique global company, founded in ****, with expertise in adding value to brands in the world of labels, packaging and accessories. We take pride in being a "Development Hub" for both brand owners and garment manufacturers alike - offering complete, creative and made concepts in the areas of branding, design, product development and logistics solutions.Our offices and...

In a nutshell Position: Deputy Technical Director of Quality Location: Valencia Experience: 5+ years in leadership roles within pharmaceutical FDF manufacturing Want to know more? Bio Nano Pharma is a global company committed to excellence across the pharmaceutical value chain, bringing innovation, quality, and expertise in research, development, manufacturing, and distribution of pharmaceutical...

About Us Legit.Health deploys computer vision and artificial intelligence technology to enable lifesaving diagnosis and therapies for visible diseases. Our goal is to enable universal access to high-quality diagnosis and follow-up of pathologies and to offer affordable health assistance to everyone everywhere. Things to Know We are a startup, it is important that you are knowledgeable about how...

Quality Engineer We are now looking for aQuality Engineer to join our team working for a better future. The position is permanent and the preferred location is in Porriño, Spain. What you will be doing As Quality Engineer, your work will focus on these responsibilities: Collaborate effectively with project management to ensure the availability of resources to achieve quality goals. Define clear...

Position Overview Review, analyze, and compose responses to regulatory agencies regarding medical device reportable events and collaborate both within post market surveillance and across other functions, including customer care, quality, clinical and regulatory to help ensure compliance with reporting requirements and good documentation practices. This position reports to the Director EMEA...

In a nutshell Position: Director of Quality Assurance Location: Paterna (Valencia) – On-site Experience: 5+ years in quality leadership within pharmaceutical FDF manufacturing Want to know more? Bio Nano Pharma is committed to excellence in the development, manufacturing, and distribution of innovative pharmaceutical products. Our mission is to ensure the highest standards of quality and safety...

Nilorn Portugal, based in Recarei-Paredes, one of the key units within Nilorn Worldwide, is actively hiring. Nilorn Worldwide is a unique global company, founded in ****, with expertise in adding value to brands in the world of labels, packaging and accessories. We take pride in being a "Development Hub" for both brand owners and garment manufacturers alike - offering complete, creative and made...

Position Overview Review, analyze, and compose responses to regulatory agencies regarding medical device reportable events and collaborate both within post market surveillance and across other functions, including customer care, quality, clinical and regulatory to help ensure compliance with reporting requirements and good documentation practices. This position reports to the Director EMEA...