ppJoin Roche as an International Regulatory Affairs Professional to drive regulatory solutions for global IVD/MD instruments and software. Bring your expertise in regulatory strategy, compliance, and cross‑functional collaboration to impact patient care worldwide. /p h3Key Responsibilities /h3 ul liLead and support regulatory strategies for global IVD/MD instrument and software submissions. /li liEnsure compliance with international regulatory requirements and standards. /li liCollaborate with cross‑functional teams (RD, Quality, Clinical) to drive regulatory initiatives. /li liProvide regulatory guidance to support product development and lifecycle management. /li liStay abreast of evolving regulatory trends and implement best practices. /li /ul h3Requirements /h3 ul liBachelor’s Degree in Life Sciences, Regulatory Affairs, or related field. /li li5 to 7 years of experience in Regulatory Affairs (Regulatory, RD, Quality, and/or Clinical), preferably in healthcare regulatory affairs.



/li liIn‑depth knowledge of general regulatory requirements, guidelines, and procedures for IVD instruments and software. /li liStrong organizational and communication skills. /li liAbility to multitask and manage multiple projects simultaneously. /li liSelf‑motivated and able to work independently in a self‑management environment. /li liExperience with IVD instrument and/or software development. /li /ul h3Benefits /h3 ul liCollaborative and innovative work environment. /li liOpportunity to make a meaningful impact on patients’ lives globally. /li liCompetitive compensation and benefits package. /li liProfessional development and growth opportunities within a leading global healthcare organization. /li /ul pbRoche is an Equal Opportunity Employer. /b /p /p #J-18808-Ljbffr

📌 Regulatory Affairs Manager (San Cugat del Vallés)
🏢 Roche
📍 San Cugat del Vallés