Regulatory Affairs Specialist

{"title": "Regulatory Affairs Specialist", "content": "Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at ResMed Inc. in Sydney, Australia. As a key member of our Regulatory Affairs - Systems and Business Excellence Team, you will play a critical role in ensuring the compliance of our medical devices with global...

Job DescriptionJob Title: Regulatory Affairs SpecialistJob Summary:We are seeking a highly skilled Regulatory Affairs Specialist to join our team at ResMed Inc. The successful candidate will be responsible for ensuring the regulatory compliance of our medical devices and providing support to our internal stakeholders and external regulators.Key...

Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at ResMed Inc. as a Specialist, Regulatory Postmarket Compliance. This role will be responsible for leading regulatory affairs strategy to ensure compliance with postmarket regulations and quality standards.Key ResponsibilitiesDevelop and implement regulatory postmarket...

{"h1": "Regulatory Affairs Specialist", "p": "At Device Technologies Australia Pty Ltd, we are seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory affairs team, you will be responsible for ensuring the quality, safety, and efficacy of our medical devices throughout their life cycle.Your key...

Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at ResMed Inc. as a Regulatory Affairs - Systems and Business Excellence Team member. The successful candidate will be responsible for ensuring the continuance of regulatory compliance of existing ResMed products, reviewing new and changing policies, regulations, and...

Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at ResMed Inc. As a key member of our Global Product Regulatory Affairs function, you will play a critical role in ensuring the compliance of our medical devices with regulatory requirements.Key ResponsibilitiesDevelop and implement regulatory postmarket strategies to...

Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at ResMed Inc. As a key member of our Global Product Regulatory Affairs function, you will play a critical role in ensuring the compliance of our medical devices with regulatory requirements.Key ResponsibilitiesDevelop and implement regulatory postmarket strategies to...

Job SummaryThe Regulatory Affairs Specialist will lead regulatory affairs strategy to be aligned with objectives of our post market products. This role will be responsible for planning and coordinating regulatory post market strategies, representing Regulatory Affairs on selected post market cross-functional teams, and developing and implementing submissions...

{"h1": "Regulatory Affairs Coordinator", "p": "At ResMed Inc, we are seeking a highly skilled Regulatory Affairs Coordinator to support our regulatory affairs team in ensuring compliance with local, regional, and international regulations for medical devices. This role involves assisting in the preparation of regulatory documents, maintaining records, and...

{"title": "Medical Devices Regulatory Affairs Associate", "subtitle": "Join Our Team", "content": "We are seeking a highly skilled Medical Devices Regulatory Affairs Associate to join our team in Australia. As a key member of our Medical Devices Consulting team, you will play a critical role in ensuring the regulatory compliance of our clients' products.Your...

Job SummaryWe are seeking a highly skilled Regulatory Affairs Coordinator to support our regulatory affairs team in ensuring compliance with local, regional, and international regulations for medical devices.Key ResponsibilitiesRegulatory Submissions: Assist in the preparation of regulatory documentation for product registrations, amendments, and renewals in...

Job Summary:The Regulatory Affairs Coordinator supports the regulatory affairs team in ensuring compliance with local, regional, and international regulations for medical devices.Key Responsibilities:Regulatory Submissions: Assist in the preparation of regulatory documentation for product registrations, amendments, and renewals in compliance with global...

About the RoleAs a key member of our Regulatory Affairs team at On Q Recruitment, you'll play a pivotal role in supporting the compliance of healthcare products with legal and industry standards. You'll provide strategic regulatory advice, manage submissions, and maintain compliance for our product portfolios, ensuring that they align with business...

Senior Regulatory Affairs AssociateStryker Australia Pty Ltd is seeking a highly skilled and experienced Senior Regulatory Affairs Associate to join our high-performing regulatory team. As a key member of our team, you will play a critical role in ensuring compliance with regulatory requirements and driving business growth.Key Responsibilities:Prepare and...

Regulatory Affairs & Quality Assurance ManagerAre you a seasoned professional looking for a new challenge in the medical devices industry? We have an exciting opportunity for a Regulatory Affairs & Quality Assurance Manager to join our team at Hengandhurst.About the RoleWe are seeking a highly motivated and experienced individual to lead our regulatory...

Job Summary:The Regulatory Affairs Coordinator supports the regulatory affairs team in ensuring compliance with local, regional, and international regulations for medical devices. This position involves assisting in the preparation of regulatory documents, maintaining records, and coordinating with various departments to support product registrations and...

About the RoleWe are seeking a highly skilled Senior Regulatory Affairs Associate to join our team at Johnson & Johnson. As a key member of our Regulatory Affairs team, you will play a critical role in supporting the development and submission of regulatory applications for our products in Australia and New Zealand.Key ResponsibilitiesLead a portfolio of...

Job SummaryWe are seeking a highly skilled Regulatory Affairs Coordinator to join our team at ResMed Inc. The successful candidate will be responsible for ensuring compliance with local, regional, and international regulations for medical devices.Key ResponsibilitiesRegulatory Submissions: Assist in the preparation of regulatory documentation for product...

About the Role: As a Regulatory Affairs Associate with the Healthcare Professionals Group, you will play a crucial role in ensuring the compliance and registration of our products in the Australian market. This is a 12-month contract opportunity that will challenge and develop your skills in regulatory affairs.Key Responsibilities: • Manage the transfer of...

About the RoleIn this key position, you will be responsible for ensuring the daily operations of regulatory affairs and guaranteeing regulatory submission compliance. You will create and manage submission documents for new products or changes to existing regulatory submissions.Develop and submit regulatory documents for the ANZ marketReview and approve...