Regulatory Affairs Associate/IVDR

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Accountability / Scope:As the professional in the Regulatory Affairs function, the individual will assist teams in the registration of products by preparing documentation needed for registration in EURI/MENAP global.Individual shall develop partnership with other regulatory functions, affiliates & other stakeholder to define plan & strategy for submissions...

Accountability / Scope: As the professional in the Regulatory Affairs function, the individual will assist teams in the registration of products by preparing documentation needed for registration in EURI/MENAP global. Individual shall develop partnership with other regulatory functions, affiliates & other stakeholder to define plan & strategy for...

Project Manager - IVDR - Performance Evaluation CoordinatorThis candidate needs to have strong Medical Device exp (no Pharma/Bio) and has a good medical writing/technical writing background.They will be evaluating documentation and needs to be strong with performance evaluations, document creation and have a demonstrated PM background to manage this...

Project Manager - IVDR - Performance Evaluation CoordinatorThis candidate needs to have strong Medical Device exp (no Pharma/Bio) and has a good medical writing/technical writing background.They will be evaluating documentation and needs to be strong with performance evaluations, document creation and have a demonstrated PM background to manage this...

Project Manager - IVDR - Performance Evaluation CoordinatorThis candidate needs to have strong Medical Device exp (no Pharma/Bio) and has a good medical writing/technical writing background.They will be evaluating documentation and needs to be strong with performance evaluations, document creation and have a demonstrated PM background to manage this...

Accountability / Scope:As the professional in the Regulatory Affairs function, the individual will assist teams in the registration of products by preparing documentation needed for registration in EURI/MENAP global. Individual shall develop partnership with other regulatory functions, affiliates & other stakeholder to define plan & strategy for submissions...

DivIHN (pronounced "divine") is a CMMI ML3-certified Technology and Talent solutions firm. Driven by a unique Purpose, Culture, and Value Delivery Model, we enable meaningful connections between talented professionals and forward-thinking organizations. Since our formation in 2002, organizations across commercial and public sectors have been trusting us to...

Job Description The Associate Director, RA Global Regulatory Strategy, US & Canada (Oncology) is responsible for the development and implementation of US and Canada regulatory strategic and tactical planning (RSTP) for assigned on market products or those products in development. This individual demonstrates the ability to combine knowledge of scientific,...

Opportunity to join a global diagnostics company at their HQ just outside of Chicago, focused on the strategy for existing and new product submissions to the FDA and Canada. Leading a small team, this is for somebody with prior Regulatory management experience and knowledge of IVD requirements.Main ResponsibilitiesLead the US & Canada Regulatory team to...

Opportunity to join a global diagnostics company at their HQ just outside of Chicago, focused on the strategy for existing and new product submissions to the FDA and Canada. Leading a small team, this is for somebody with prior Regulatory management experience and knowledge of IVD requirements.Main ResponsibilitiesLead the US & Canada Regulatory team to...

Opportunity to join a global diagnostics company at their HQ just outside of Chicago, focused on the strategy for existing and new product submissions to the FDA and Canada. Leading a small team, this is for somebody with prior Regulatory management experience and knowledge of IVD requirements.Main ResponsibilitiesLead the US & Canada Regulatory team to...

Job Description Take the next step in your career with an organization that strategically invests in the long-term health of the company, its technology and its people. The AbbVie Business Technology Solutions (BTS) team shapes the digital transformation necessary for our treatments to positively impact patients’ lives.  Join our collaborative and global...

Job Description Opportunity at a Glance The Senior Regulatory Affairs Analyst is responsible for interpreting statutes, regulations and administrative rules of various issuing bodies and developing procedures and processes to assure compliance with those rules and monitoring the performance of those procedures and processes. The senior analyst will serve...

Job Description Opportunity at a Glance The Senior Regulatory Affairs Analyst is responsible for interpreting statutes, regulations and administrative rules of various issuing bodies and developing procedures and processes to assure compliance with those rules and monitoring the performance of those procedures and processes. The senior analyst will serve...

Job Description The Associate Director, Regulatory Affairs, Strategic Global Labeling – Combination Products and Devices, combines the knowledge of scientific, regulatory, and business issues to support labeling for products that are developed, manufactured or distributed to meet required legislation. This individual has influence within the department...

Job Description Job Description Job Title: Regulatory SpecialistDuration: 6 months (Potential extension)Location: Hybrid - Chicago, IL 60642Summary:As a member of the Scientific & Regulatory Affairs (SRA) team, this role focuses on screening, tracking, and managing regulatory information related to ingredients. Ensuring the accuracy and completeness of...

Job Description Job Description Job Title: Regulatory Specialist Duration: 6 months (Potential extension) Location: Hybrid - Chicago, IL 60642 Summary: As a member of the Scientific & Regulatory Affairs (SRA) team, this role focuses on screening, tracking, and managing regulatory information related to ingredients. Ensuring the accuracy and completeness of...

Job Title: Regulatory Specialist Duration: 6 months (Potential extension) Location: Hybrid - Chicago, IL 60642 Summary As a member of the Scientific & Regulatory Affairs (SRA) team, this role focuses on screening, tracking, and managing regulatory information related to ingredients. Ensuring the accuracy and completeness of ingredient data is crucial for...

Job Description   Senior Manager Medical Affairs Quality Assurance is responsible for providing independent quality oversight of GxP activities executed by AbbVie’s Medical Affairs enterprise, including but not limited to non-interventional studies, medical information and other regulatory commitments., covering the AbbVie drug, device and cosmetic...