Regulatory Affairs Specialist - Fort Worth

We are seeking a Regulatory Affairs Specialist II to support the European Union In Vitro Diagnostic Regulation (IVDR) transition efforts impacting Bio-Rad products currently CE-marked under the IVD Directive. · Bachelor's degree in Biochemistry, Biology, Medical Technology , or a ...

The Regulatory Affairs Specialist supports IVDR project revisions of assigned technical files. · Supports IVDR project by revising technical files. · Supports IVDR labeling conversion project. · ...

Support the EU's In Vitro Diagnostic Regulation (IVDR) transition activities and prepare technical files for Client's products. · Revision of technical files when needed update labeling to comply with IVDR requirements track RA Regional notifications and other related activities ...

Join our client's Regulatory Affairs team to support the transition to the EU's In Vitro Diagnostic Regulation (IVDR). This role plays a critical part in ensuring regulatory compliance by revising technical documentation, updating labeling, and coordinating regional notifications ...

Regulatory affairs specialist with working knowledge of FDA and CE marking requirements for IVD products. · Support the IVDR project by revising assigned technical files and labeling conversion project which requires cross-functional participation. · Support the IVDR project by ...

The candidate will support the EU's In Vitro Diagnostic Regulation (IVDR) transition activities that will impact all Client's products currently CE Marked under the IVD Directive. The tasks include preparing revision of technical files when needed, updating labeling to comply wit ...

We are seeking a Public Affairs Specialist II to support our media relations and communications strategies. · ...

Supports and contributes to the company's media relations and communications strategies helping drive dialogue creating storytelling opportunities with key internal and external stakeholders that elevate the GM Financial brand and support our parent company General Motors. · Supp ...

Support the EU's In Vitro Diagnostic Regulation (IVDR) transition activities that will impact all Bio-Rad products currently CE Marked under the IVD Directive. · Revising technical files for assigned productsUpdating labeling specifications to meet IVDR requirementsTracking RA Re ...

Support the EU's In Vitro Diagnostic Regulation (IVDR) transition activities that will impact all company products currently CE Marked under the IVD Directive. · ...

Supports and contributes to the company's media relations and communications strategies. · Solid understanding of media relations tools, techniques and best practices · Experience with developing media relations and corporate communications materials · ...

Support the EU's In Vitro Diagnostic Regulation (IVDR) transition activities. · Revisar los archivos técnicos asignados para cumplir con los requisitos del IVDR. · Actualizar la etiquetado de productos para cumplir con los requisitos del IVDR. · ...

Support the EU's In Vitro Diagnostic Regulation (IVDR) transition activities that will impact all Bio-Rad products currently CE Marked under the IVD Directive. · ...

Support the EU's In Vitro Diagnostic Regulation (IVDR) transition activities that will impact all Bio-Rad products currently CE Marked under the IVD Directive. · ...

This team empowers the business to move forward with clarity and purpose, · ensuring we deliver on our mission with integrity and impact.If you're passionate about making a difference through strategy, · collaboration and creativity, Public Relations & Policy is where your impact ...

This role supports the EU's In Vitro Diagnostic Regulation (IVDR) transition activities that will impact all Bio-Rad products currently CE Marked under the IVD Directive. · ...

We are currently seeking a Senior Regulatory Affairs Specialist to join our Endoscopy Business Unit based in Flower Mound,TX. · ...

We are currently seeking a Senior Regulatory Affairs Specialist to join our Endoscopy Business Unit based Hybrid in Flower Mound TX. As the Senior Regulatory Affairs Specialist you support new product development and sustaining for both US and OUS global regulatory release throug ...

We are seeking a Regulatory Affairs Associate Specialist to support McKesson's Controlled Substances Monitoring Program (CSMP). The role will provide administrative support to the Regulatory Affairs Department, conduct initial customer due diligence, and use tools, reports, and d ...

We are seeking a Regulatory Affairs Associate Specialist. This role is a work-from-home position in the Dallas-Fort Worth Metropolitan area. If the applicant is located outside of the area, they must be willing to relocate. · Responsibilities:Organize and coordinate incoming regu ...