Senior Regulatory Affairs Specialist.

Transformative Career OpportunityWe are seeking a highly skilled and innovative Regulatory Affairs Specialist to join our dynamic team at Medtronic. As a key member of our team, you will play a pivotal role in ensuring compliance with regulatory requirements and driving process improvements.About the RoleAs a Regulatory Affairs Specialist, you will be...

Transformative Career OpportunitiesWe're seeking a highly skilled and innovative professional to join our dynamic team at Medtronic. As a Senior Regulatory Affairs Specialist, you'll collaborate with subject matter experts and project/process improvement colleagues to drive meaningful change and growth.About the RoleAs a key member of our team, you'll be...

Job Title: Senior Regulatory Affairs SpecialistJob Summary:This position is responsible for coordinating, preparing, and maintaining regulatory submissions and documents on a global level, for Saudi Arabia and GCC region. The primary responsibilities include ensuring regulatory compliance for assigned countries as Merit evolves. Other responsibilities...

Transformative Career OpportunityWe're seeking a highly skilled and innovative professional to join our dynamic team at Medtronic. As a Senior Regulatory Affairs Specialist, you will play a pivotal role in ensuring compliance with the Medical Device Regulation (MDR) and driving meaningful change within our organization.A Day in the Life• Conduct thorough...

About the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Medtronic. As a key member of our regulatory team, you will play a critical role in ensuring compliance with regulatory requirements and ensuring the quality of our products.Key ResponsibilitiesReview and enhance QA structures to ensure compliance with regulatory...

{"title": "Regulatory Affairs Expert", "content": "At Medtronic, we're seeking a highly skilled Regulatory Affairs Expert to join our team. As a key member of our regulatory team, you'll play a pivotal role in ensuring compliance with the Medical Device Regulation (MDR) and navigating complex QA structures.A Day in the Life• Conduct thorough reviews of...

Job SummaryThis role is responsible for ensuring regulatory compliance for assigned countries as Merit evolves. The successful candidate will coordinate, prepare, and maintain regulatory submissions and documents on a global level, with a focus on the Saudi Arabia and GCC region.Key ResponsibilitiesDetermine global regulatory pathways for various projects,...

Job SummaryThis position is responsible for coordinating, preparing, and maintaining regulatory submissions and documents on a global level, for Saudi Arabia and GCC region. The primary responsibilities include ensuring regulatory compliance for assigned countries as Merit evolves. Other responsibilities include product life cycle management in accordance...

Job SummaryThis role is responsible for ensuring regulatory compliance for assigned countries as Merit Medical Systems, Inc. evolves. The successful candidate will coordinate, prepare, and maintain regulatory submissions and documents on a global level, with a focus on the Saudi Arabia and GCC region.Key ResponsibilitiesDetermine global regulatory pathways...

Job SummaryThis position is responsible for coordinating, preparing, and maintaining regulatory submissions and documents on a global level, for Saudi Arabia and GCC region. Primary responsibilities include ensuring regulatory compliance for assigned countries as Merit evolves. Other responsibilities include product life cycle management in accordance with...

Job SummaryThis position is responsible for coordinating, preparing, and maintaining regulatory submissions and documents on a global level, for Saudi Arabia and GCC region. Primary responsibilities include ensuring regulatory compliance for assigned countries as Merit evolves. Other responsibilities include product life cycle management in accordance with...

Job Description SUMMARY OF DUTIES This position is responsible for coordinating, preparing, and maintaining regulatory submissions and documents on a global level, for Saudi Arabia and GCC region. Primary responsibilities are to ensure regulatory compliance for assigned countries as Merit evolves. Other responsibilities include product life cycle...

About the RoleThis is an exciting opportunity to join Medtronic as a Senior Clinical Research Specialist. As a key member of our team, you will be responsible for the development and execution of clinical studies, as well as developing and overseeing clinical strategies for assessing product safety and effectiveness.Key ResponsibilitiesOversee the...

Careers that Change Lives Are you ready for this exciting role as a Senior Clinical Research Specialist (CRS) you will have primary responsibility in the development and execution of clinical studies and for developing and overseeing clinical strategies for effectively assessing performance related to the ongoing evaluation of product safety and...

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Job Title: Quality Assurance SpecialistTrento Engineering is seeking a highly skilled Quality Assurance Specialist to join our team. As a Quality Assurance Specialist, you will be responsible for ensuring that our products meet the highest standards of quality and safety.Key Responsibilities:Develop and implement quality control procedures to ensure...

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About the RoleWe are seeking a highly motivated and experienced Clinical Research Specialist to join our team at Medtronic. As a Clinical Research Specialist, you will be responsible for conducting clinical studies in compliance with applicable clinical and regulatory standards and in alignment with Medtronic business needs.Key ResponsibilitiesDesign, plan,...