Regulatory Affairs Consultant

We are seeking a skilled Regulatory Consultant to join our Clinical and Regulatory Team. As a key member, you will work on regulatory consulting projects, leveraging your expertise in data monitoring, content authoring, and regulatory landscape analysis.About YouBachelor's or master's degree in pharmaceutical sciencesAt least 5 years of relevant work...

We are seeking a highly skilled Regulatory Solutions Consultant to join our Clinical and Regulatory Team. This is an exciting opportunity to work on regulatory consulting projects, leveraging your expertise in data monitoring, content writing, and consulting for multiple domains.About YouBachelor's or master's degree in pharmaceutical sciencesAt least 5...

At ES16 Alcon Healthcare S.A. Company, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you'll be recognized for your commitment and contributions and see your career like never before.The Regulatory Affairs Manager is responsible for...

At ES16 Alcon Healthcare S.A. Company, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you'll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact...

We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Clarivate.About the RoleThis is a permanent full-time position that offers a competitive salary of $90,000 - $110,000 per year, depending on experience. The working schedule is flexible, mostly centered on CET time zone with occasional need to accommodate late or early meetings...

At ES16 Alcon Healthcare S.A. Company, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care.The Regulatory Affairs Specialist for Medical Devices is responsible for preparing high-quality and timely regulatory applications and notifications to...

About the RoleWe are seeking an experienced Content Manager to join our team in Barcelona. As a key member of our Content Function, you will be responsible for managing a global team and driving the execution and performance of our content operations.About the TeamYou will be reporting to the Director, Content Editing, Regulatory and Market Access, based in...

We are seeking a highly skilled Implementation Consultant to join our Product team in Barcelona. As an Implementation Consultant, you will be responsible for interacting with our customers, working closely with global accounts and their internal teams to implement Drug Safety Triager (DST). The Drug Safety Triager is our next-generation pharmacovigilance...

About the RoleDow Jones Risk & Compliance is a global provider of third-party risk management and regulatory compliance solutions.We deliver data, research tools and services to help our clients meet anti-money laundering, anti-bribery, anti-corruption and economic sanctions regulations and mitigate third-party risk.Your ResponsibilitiesLead and develop a...

About the RoleDow Jones Risk & Compliance is a global provider of third-party risk management and regulatory compliance solutions. We deliver data, research tools and services to help our clients meet anti-money laundering, anti-bribery, anti-corruption and economic sanctions regulations and mitigate third-party risk.As a Team Lead for Sanctions Control and...

We are looking for a RAQA Consultant ( Regulatory Affairs / Quality Assurance ) to join our Clinical and Regulatory Team. This is an amazing opportunity to work on regulatory and quality consulting projects. We have a great skill set in data monitoring, content writing and consulting for multiple domains- regulatory submissions, clinical trials,...

At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our...

We are looking for a Regulatory Solutions Consultant to join our Clinical and Regulatory Team. This is an amazing opportunity to work on regulatory consulting projects. We have a great skill set in data monitoring, content writing and consulting for multiple domains- regulatory submissions, clinical trials, marketing authorization applications (MAA),...

**Job Description Summary**: As Regulatory Affairs Trainee you will learn and develop from executing and supporting the activities of the Regulatory Affairs Operations team. The scope extends across BD business units and all EMEA countries. The activities are related with regulatory responsibilities to execute regulatory processes and provide support (with...

At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our...

Centrient Pharmaceuticals is the leading manufacturer of beta-lactam antibiotics, and a provider of next generation statins and anti-fungals. We produce and sell intermediates, active pharmaceutical ingredients and finished dosage forms. We stand proudly at the centre of modern healthcare, as a maker of essential and life-saving medicines. With our...

QbD Groupteam offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution for companies active in Pharma, ATMP and Medical Devices/IVD. We are always looking for the next QbD'er in Regulatory Affairs. What do we expect from you as a Senior Regulatory Affairs Officer? You have knowledge of...

QbD Groupteam offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution for companies active in Pharma, ATMP and Medical Devices/IVD.We are always looking for the next QbD'er in Regulatory Affairs.What do we expect from you as a Senior Regulatory Affairs Officer?You have knowledge of...

QbD Groupteam offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution for companies active in Pharma, ATMP and Medical Devices/IVD. We are always looking for the next QbD’er in Regulatory Affairs.What do we expect from you as a Senior Regulatory Affairs Officer? You have knowledge of...

**FDF REGULATORY AFFAIRS OFFICER** Nuestro cliente es una compañía farmacéutica española cuyo negocio está centrado en I+D, licencia, fabricación y suministro de productos farmacéuticos. Cuenta con un amplio conocimiento y experiência en ofrecer productos y soluciones de calidad en el ecosistema de la salud. Sus valores abanderan un alto compromiso...

We are looking for Implementation Consultant to join our Product team in Barcelona. As Implementation Consultant you’ll be interacting with our customers. This is a great opportunity to work with our global accounts and their internal teams to implement Drug Safety Triager (DST). The Drug Safety Triager is our next-generation pharmacovigilance (PV)...

**Global Responsability**: Support new regulatory submissions and assisting with the lifecycle management of the existing portfolio making sure that any variations and/or renewals will be submitted in time to ensure regulatory compliance. **Specific Responsibilities**: Support and provide the necessary documentation to local affiliates and clients for...

Location- El Prat de Llobregat- Type of contract- Permanent Full Time- Occupational field- Auditing & Consulting- Job-ID- 5279- Job Description- As a Product Specialist/Expert you evaluate IVD Expert medical products in accordance with European guidelines and standards. - You are responsible for the review of the technical documentation of selected product...

**Somos Top Employer 2022** En Synthon vivirás una gran experiência, en un ambiente laboral excelente, y rodeado de personas con alto talento y motivación, donde podrás aportar colaborando con el resto del equipo para conseguir los resultados de la Compañía, y desarrollarte profesional y personalmente. - Soporte en la preparación de documentación de...

Location- El Prat de Llobregat- Type of contract- Permanent Full Time- Occupational field- Medicine & Healthcare- Job-ID- 11851- Job SummaryEvaluates complex medical devices with medium risk and the according documentation. - Job Description- Evaluates complex medical products according to the relevant technical regulations and relevant EC directives,...

Study Start Up Associate II - Fluent Dutch Required ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development Study Start Up Associate / Regulatory...

Description Senior Medical Writer Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.Our Clinical Development model brings the customer and the patient to the center of...

Description Job Title: Manager, Sanctions Control & Ownership, Risk & Compliance Research About the Role Dow Jones Risk & Compliance is a global provider of third-party risk management and regulatory compliance solutions. We deliver data, research tools and services to help our clients meet anti-money laundering, anti-bribery, anti-corruption and...

**General information**: - Location - El Prat de Llobregat - Type of contract - Permanent Full Time - Occupational field - Auditing & Consulting - Job-ID - 5279 - As a Product Specialist/Expert you evaluate IVD Expert medical products in accordance with European guidelines and standards. You are responsible for the review of the technical documentation of...

**General information**: - Location - El Prat de Llobregat - Type of contract - Permanent Full Time - Occupational field - Medicine & Healthcare - Job-ID - 11851 **Job Summary**: Evaluates complex medical devices with medium risk and the according documentation. - Evaluates complex medical products according to the relevant technical regulations and...