Quality and Regulatory associate Junior
hace 1 semana
Mediktor is looking for a QA/RA specialistIf you are passionate about applying the regulation to cutting edge technology and you would like to discover the Software Medical Device regulation, we are looking for youThe Team:As a member of the Quality Department, you will collaborate closely with all teams and departments at Mediktor, supporting them in meeting regulatory and quality requirements. You will play a key role in the implementation and maintenance of an integrated management system, ensuring effective compliance with the AI Act, MDR, and accessibility standards across the organization.Responsibilities:Manage and update Integrated Management System documentation to ensure organization-wide compliance.Participate in internal and external audits to verify adherence to quality standards.Partner with teams to integrate and uphold quality requirements across departments.Validation & Risk: Execute and oversee the validation systems and the risk management framework to mitigate operational gaps.Direct the CAPA and Change Order processes to drive continuous improvement.Execute supplier evaluations to ensure high-quality procurement standards.Strategic Support: Perform additional duties and key projects as assigned.Requirements:Life Science Degree studiesFluent in English and SpanishStrong attention to detailExcellent communication and interpersonal skills, and a desire to learn and grow professionallyAt least 1 year of experience in a QA/RA role (including trainee position)We Are Looking For Someone With a curious mind to be up to date of what is going on in the company and the trends and innovations of the sector. What you will find working with Mediktor: An exciting scale-up company sharing good vibes & excellent multicultural and team working environment
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Quality and Regulatory associate Junior
hace 1 semana
Catalonia, España Mediktor A tiempo completoMediktor is looking for a QA/RA specialist! If you are passionate about applying the regulation to cutting edge technology and you would like to discover the Software Medical Device regulation, we are looking for you! The Team: As a member of the Quality Department, you will collaborate closely with all teams and departments at Mediktor, supporting them in...
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Quality and Regulatory Director
hace 5 días
Catalonia, España ARTO A tiempo completoPosition Overview The Director of Quality and Regulatory Affairs will play a central role in defining and executing the organization's overall quality and regulatory roadmap. This position oversees the Quality Control, Quality Assurance, and Regulatory Affairs functions, ensuring that operations, systems, and products consistently meet applicable GxP and...
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Quality and Regulatory Director
hace 5 días
Catalonia, España ARTO A tiempo completoPosition Overview The Director of Quality and Regulatory Affairs will play a central role in defining and executing the organization's overall quality and regulatory roadmap. This position oversees the Quality Control, Quality Assurance, and Regulatory Affairs functions, ensuring that operations, systems, and products consistently meet applicable GxP and...
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Quality and Regulatory associate Junior
hace 1 semana
Catalonia, España Mediktor A tiempo completoMediktor is looking for a QA/RA specialist!If you are passionate about applying the regulation to cutting edge technology and you would like to discover the Software Medical Device regulation, we are looking for you!The Team:As a member of the Quality Department, you will collaborate closely with all teams and departments at Mediktor, supporting them in...
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Quality regulatory manager
hace 1 semana
Catalonia, España Elemed A tiempo completoTitle: RAQA Lead - Spain and Portugal Location: Barcelona, Spain Contact: The company Are you someone who has Iberia-wide regulatory experiences and are looking for the next step in your medical devices career at the EMEA level? Are you someone who likes to think creatively and prioritizes medical devices that are always accessible to patients and surgeons...
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Regulatory Affairs Associate
hace 2 semanas
Catalonia, España Vetpharma A tiempo completoWho we are? Veterinary medicine manufacturers Vetpharma is the veterinary division of Chemo, part of the Insud Pharma group, providing Animal Health solutions. We are located in Barcelona, where the group was founded in 1977. In Vetpharma we are a highly qualified team. We have extensive experience in development, registration and marketing veterinary...
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Regulatory affairs associate
hace 1 semana
Catalonia, España Vetpharma A tiempo completoWho we are? Veterinary medicine manufacturers Vetpharma is the veterinary division of Chemo, part of the Insud Pharma group, providing Animal Health solutions. We are located in Barcelona, where the group was founded in 1977. In Vetpharma we are a highly qualified team. We have extensive experience in development, registration and marketing veterinary...
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Quality Technician
hace 3 semanas
Catalonia, España Uplift People Consulting A tiempo completoAbout Uplift Uplift is a dynamic agency specializing in global talent search, covering EMEA, LATAM, USA, and APAC. With successful placements in 52 countries, we combine speed and cutting-edge technology to source top executive and mid-senior talent across various functions. Our innovative approach integrates global networks, AI, and advanced recruitment...
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Regulatory Affairs Manager CMC
hace 2 semanas
Catalonia, España Oxford Global Resources A tiempo completoOxford Global Resources is seeking a Global CMC Regulatory Affairs Manager Consultant to support as external contractor on behalf of Oxford a top leading pharma company to support headquartered in Barcelona through our consulting services division.Key Responsibilities:Provide CMC regulatory insight and advice to multidisciplinary teams, as well as CMC...
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Regulatory Affairs Manager
hace 2 días
Catalonia, España Hezuo Ltd A tiempo completoAs Regulatory Affairs Manager, you'll play a pivotal role in supporting the geographical expansion of a dietary supplement ingredient business. Based in Barcelona, you'll coordinate regulatory activities that ensure timely and compliant product registrations, authorizations, marketing & scientific communication across international markets, while providing...
