Ivdr - 22+ job offers

Advantage Technical

A leading life sciences organization is seeking a Regulatory Affairs Specialist focused on IVDR to ensure compliance with new regulations. The role involves preparing technical files, collaborating with cross-functional teams, and managing regulatory documentation. Ideal candidates should possess a

Bio-Rad Laboratories

A leading scientific products firm located in California is seeking a Regulatory Affairs Associate to support the transition activities related to the EU's In Vitro Diagnostics Regulation (IVDR). You will revise technical files, assist in labeling conversions, and ensure compliance with regulatory r

Tri-Valley Career Center

A leading life science company located in California seeks a professional to support their In Vitro Diagnostic Regulation transition activities. In this role, you will work on the revision of technical files, labeling updates, and compliance with IVDR requirements. Candidates should possess a Bachel

A company is looking for a Global Team Leader - IVDR. Key Responsibilities Lead the team of IVDR product assessors and manage the in vitro diagnostic medical device training process Provide technical expertise and support for the in vitro diagnostic medical device conformity assessment process Devel

Advantage Technical

A leading technical staffing agency is seeking a Regulatory Affairs Specialist II to join their team in California. This role involves supporting the transition to the EU’s In Vitro Diagnostic Regulation by revising technical documentation, updating labeling, and ensuring regulatory compliance. The

Advantage Technical

A leading life sciences organization is seeking a Regulatory Affairs Specialist focused on IVDR to ensure compliance with new regulations. The role involves preparing technical files, collaborating with cross-functional teams, and managing regulatory documentation. Ideal candidates should possess a

Advantage Technical

A leading technical staffing agency is seeking a Regulatory Affairs Specialist II to join their team in California. This role involves supporting the transition to the EU’s In Vitro Diagnostic Regulation by revising technical documentation, updating labeling, and ensuring regulatory compliance. The

A global healthcare leader is seeking a Regulatory Specialist II to prepare EU Technical Files and support international product registrations for in vitro diagnostic medical devices. The ideal candidate will possess a Bachelor's degree in a relevant field, along with at least 4 years of regulatory

A pioneering healthcare technology company is seeking a Lead Quality Engineer in New York. This role involves ensuring the quality assurance of medical devices and laboratory developed tests, overseeing cross-functional team compliance with FDA and EU regulations, and managing post-market surveillan

A leading healthcare solutions provider is seeking an Associate Medical Writer to support regulatory-compliant performance evaluation reports for IVD products. This remote role requires strong writing and regulatory experience, particularly in compliance with EU IVDR. The ideal candidate will work c

A leading biotech company is seeking a Regulatory Affairs Officer based in Houston, Texas. The role involves developing and maintaining ISO 13485-compliant Quality Management Systems and managing regulatory submissions. The ideal candidate will have over 2 years of experience in a regulated medical

A leading pharmaceutical company is seeking a Regulatory Affairs Specialist II to prepare documentation for EU Technical Files and international product registrations. Applicants should possess a Bachelor's degree in a related technical field and have over 4 years of experience in Regulatory Affairs

A leading life sciences organization is seeking a Regulatory Affairs Specialist focused on IVDR to ensure compliance with new regulations. The role involves preparing technical files, collaborating with cross-functional teams, and managing regulatory documentation. Ideal candidates should possess a

A leading technical staffing agency is seeking a Regulatory Affairs Specialist II to join their team in California. This role involves supporting the transition to the EU’s In Vitro Diagnostic Regulation by revising technical documentation, updating labeling, and ensuring regulatory compliance. The

A healthcare technology company seeks a Lead Quality Engineer in Boston to oversee quality assurance for medical devices. The role requires 5+ years of experience in the regulated industry, a BS in Engineering, and proficiency in regulatory requirements. The Lead Quality Engineer will be responsible

Regulatory Affairs Specialist (IVDR) Base pay range $45.00/hr - $50.00/hr Location: Fort Worth, TX (Onsite - local candidates only) Work Arrangement: Hybrid Third onsite day: Flexible (candidate’s choice) Contract Length: 1 year Pay Rate: $45–$50/hour (Weekly pay & Medical benefits) MUST BE LOCAL -

This range is provided by QuinTalent Inc. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range $40.00/hr - $45.00/hr Direct message the job poster from QuinTalent Inc Work Environment Hybrid - 8am - 5 pm Monday to Friday, with 3 days on

A leading global life sciences firm is seeking a Regulatory Affairs Specialist II to support the transition to EU In-Vitro Diagnostic Regulation (IVDR). The role focuses on revising documentation and ensuring compliance with regulatory standards. The ideal candidate will have a relevant Bachelor's d

A life sciences company in South Portland, Maine is seeking a Regulatory Affairs Specialist II to prepare documentation for EU Technical Files and international product registrations. The ideal candidate will have at least 4 years' experience in Regulatory Affairs and a strong understanding of IVDR

DNV is seeking a motivated and customer-oriented Sales Executive to support the growth of our medical certification services with focus in In Vitro Diagnostic Regulation (IVDR).The position will play a key role in identifying leads, engaging customers, and supporting business development activities