Senior Regulatory Affairs Specialist

Job Title Regulatory Affairs SpecialistJob title The Regulatory Affairs Specialist RA specialist coordinates and prepares regulatory plans and document packages for submissions to regulatory agencies FDA Health Canada EU Asia etc Your role Responsible for the planning coordination and preparation of document packages for regulatory submissions...

Job Title Regulatory Affairs SpecialistJob title The Regulatory Affairs Specialist RA specialist coordinates and prepares regulatory plans and document packages for submissions to regulatory agencies FDA Health Canada EU Asia etc Your role Responsible for the planning coordination and preparation of document packages for regulatory submissions...

Job DescriptionJob DescriptionJob title:The Regulatory Affairs Specialist (RA specialist) coordinates and prepares regulatory plans and document packages for submissions to regulatory agencies (FDA, Health Canada, EU, Asia, etc.).Your role:- Responsible for the planning, coordination and preparation of document packages for regulatory submissions to the US,...

About the RoleWe are seeking a highly skilled Regulatory Affairs Compliance Specialist to join our team at Frido. This is an exciting opportunity for a seasoned professional to lead our regulatory affairs efforts and ensure compliance with relevant standards.Key Responsibilities:Regulatory Compliance: Ensure adherence to ISO 13485, EN ISO 13485, USFDA, SFDA,...

JOB DESCRIPTION Job Title Senior Regulatory Affairs Manager Job Description Job Description: In this role, you will lead a Regulatory Affairs Team for our Magnetic Resonance Imaging (MRI) Business Unit, Bangalore & Pune. You will also be accountable for developing and deploying innovative, compliant regulatory strategies to grow and sustain the...

Job Title Director Regulatory Affairs IGTS-MoSDirector Regulatory Affairs IGTS-MoS Critical RA leader of the IGTS MoS Category Image Guided Therapy Systems Mobile Surgery Also a member IGTS MoS Leadership Team and advise senior management on matters concerning several functional areas and or customers Your role As the Head of Regulatory Affairs for the...

At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. R&D is committed to discovering and delivering transformational vaccines and medicines to prevent and change the course of disease. Science and technology are coming together in a way they never have before, and we have strong...

About the RoleWe are looking for an experienced Manager of Regulatory Affairs to lead our efforts in ensuring compliance with regulatory requirements. In this role, you will be responsible for monitoring all statutory compliance related to environmental management and fulfilling government authorities' requirements.You will also be responsible for...

Are you looking for a regulatory leadership role where you can build advocacy and accelerate product development and licensure on a global scale, but with a focus on US? If so, this Director, Global Regulatory Affairs, Vaccines role could be an exciting opportunity to explore. As a Director, Regulatory Affairs, Vaccines you will ensure the development and...

Job Summary : The Regulatory Specialist operates within the Product Stewardship team who are responsible for managing all regulatory matters for the global business, liaising with all global company locations and customers in Europe, Asia, North America and Latin America.The Regulatory Specialist will support in the development, implementation and...

At Frido, we are seeking a seasoned Quality Assurance Regulatory Affairs Manager to spearhead our regulatory compliance efforts.About the RoleThe ideal candidate will possess in-depth expertise in ISO 13485, EN ISO 13485, USFDA, SFDA, UKCA, and CE certification processes. A strong understanding of Quality Management Systems (QMS) and experience in their...

At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. R&D is committed to discovering and delivering transformational vaccines and medicines to prevent and change the course of disease. Science and technology are coming together in a way they never have before, and we have strong...

Job DescriptionThe Senior Regulatory Specialist will be responsible for supporting management in the day-to-day efforts related to first line of defense regulatory oversight management. This includes performing research and analyzing relevant information and transactions that warrant further investigation.Main Responsibilities:Communicating with internal and...

Job DescriptionFrido is seeking a highly skilled Regulatory Compliance Specialist to join our team.The ideal candidate will have 5-7 years of experience in Quality Assurance and Regulatory Affairs, particularly in the medical device industry. They will be responsible for ensuring adherence to regulatory standards such as ISO 13485, EN ISO 13485, USFDA, SFDA,...

Quality Assurance Regulatory Affairs ManagerThe ideal candidate is a critical thinker who will proactively improve the quality systems of the company through internal audits, participation in process improvement programs, and interaction with key partners to obtain constructive Develop standardized production, quality, and customer-service standards-...

Key Responsibilities:Regulatory Compliance: Ensure adherence to ISO 13485, EN ISO 13485, USFDA, SFDA, UKCA, and CE certification standards.Quality Management Systems (QMS): Implement and maintain robust QMS to comply with regulatory standards.Technical Documentation: Prepare and review technical files for regulatory submissions, ensuring accuracy and...

Key Responsibilities: Regulatory Compliance: Ensure adherence to ISO 13485, EN ISO 13485, USFDA, SFDA, UKCA, and CE certification standards. Quality Management Systems (QMS): Implement and maintain robust QMS to comply with regulatory standards. Technical Documentation: Prepare and review technical files for regulatory submissions, ensuring accuracy and...

Key Responsibilities: Regulatory Compliance: Ensure adherence to ISO 13485, EN ISO 13485, USFDA, SFDA, UKCA, and CE certification standards. Quality Management Systems (QMS): Implement and maintain robust QMS to comply with regulatory standards. Technical Documentation: Prepare and review technical files for regulatory submissions, ensuring accuracy and...

**About Us**Boston Scientific is a leading medical device company dedicated to advancing science for life. We are committed to solving the challenges that matter most and united by a deep caring for human life.We are seeking a highly skilled Senior Quality Assurance Specialist to join our team. The successful candidate will have a strong background in...

Frido is a leading company in the medical device industry, and we are committed to delivering high-quality products that meet regulatory requirements.About the RoleWe are seeking a highly skilled Quality Assurance Regulatory Affairs Manager to join our team. The successful candidate will have a strong background in quality management and regulatory affairs,...