Regulatory Information Management Specialist

Job Description:iGaming Licensing & Compliance SpecialistWe are seeking a highly skilled iGaming Licensing & Compliance Specialist to join our team at SOLIDICON. As an integral part of our organization, you will be responsible for ensuring our company's adherence to licensing requirements, managing regulatory certifications, and overseeing all legal...

About the Role:We are seeking a Regulatory Information Management Specialist to join our team at Randstad Life Science. As a key member of our global team, you will be responsible for ensuring efficient and seamless Regulatory Information Management across all stages. Your expertise in areas vital to successful RIM execution will enable us to stay ahead in...

Job Overview:At the Vitrolife Group, we aim to unlock the full potential of science and technology to reduce the barriers towards building a family. Our Information Security Specialist will play a crucial role in maintaining compliance, managing risks, and shaping the future of our secure and sustainable IT environment.About the Position:As an Information...

XVIVO is a global medical technology company dedicated to extending the life of organs for transplant patients.Company OverviewXVIVO is in a rapid growth phase, expanding geographically and developing new products. This position offers an opportunity to play a crucial role at the company.Job DescriptionWe are seeking a Regulatory Affairs Manager to join our...

Job Description:Randstad Life Science is seeking a highly skilled Regulatory Affairs Professional to join our team. As a key member of our global team, you will be responsible for ensuring efficient and seamless Regulatory Information Management across all stages. Your expertise in areas vital to successful RIM execution will enable us to stay ahead in the...

ResponsibilitiesAs a Mid-Senior QA/RA Specialist, your primary responsibilities will include:Be a key component of the QA/RA department with all related entities.Product inspection and testing.Host external audits and inspections.Perform internal and supplier audits.Ensure product registrations as required per market.Overall responsible for QMS.Register...

About the CompanyRandstad - Göteborg is a dynamic and rapidly growing MedTech company committed to developing innovative medical devices that improve patient outcomes. We are looking for a highly motivated and experienced Mid-Senior Quality Assurance/Regulatory Affairs (QA/RA) Specialist to join our team.This position offers an exciting opportunity to...

ResponsibilitiesThe Director of Regulatory Affairs will be responsible for leading our CBAS Regulatory team, developing and implementing global regulatory strategies, and ensuring compliance with regulatory requirements. Key responsibilities include:Strategic Planning:Develop and implement global regulatory strategies.Collaborate with cross-functional teams...

Imagine using your expertise to shape sustainable transport and infrastructure solutions for the future. As a Vehicle Safety and Compliance Specialist within Regulatory Frameworks, you will play a key role in ensuring that Volvo's products meet the highest safety standards.Responsibilities:Develop and implement regulatory compliance strategies for vehicle...

About the TeamThe Regulatory Affairs Manager will be a key member of the Compliance & Ethics Office, responsible for maintaining, enhancing, and monitoring the implementation of the trade compliance program. This includes staying up-to-date with changes in relevant laws and regulations, analyzing their impact on the company, and adjusting the compliance...

XVIVO is a rapidly growing medical technology company that develops innovative solutions to extend the life of organs for transplant patients. As a Regulatory Affairs Manager, you will play a critical role in shaping the company's future.ResponsibilitiesThe key responsibilities of this position include:Ensuring compliance with regulatory requirements for...

Job Details:The Vitrolife Group is looking for an experienced Information Security Specialist to join our team. As a key member of our global IT organization, you will play a vital role in maintaining compliance, managing risks, and shaping the future of our secure and sustainable IT environment.About the Role:As our Information Security Specialist, you will...

Cochlear, a leading medical device company, seeks a seasoned professional to lead our regulatory affairs team. As Director of Regulatory Affairs, you will be responsible for shaping and executing global regulatory strategies, ensuring compliance and timely approvals for our acoustics products in regulated markets worldwide.About the RoleKey responsibilities...

Cochlear Limited is seeking a dynamic Director of Regulatory Affairs to lead our CBAS Regulatory team based in Gothenburg, Sweden. As Director of Regulatory Affairs, you will be responsible for shaping and executing global regulatory strategies, ensuring compliance and timely approvals for our acoustics products in regulated markets worldwide.About the...

We are seeking a highly experienced professional to lead our CBAS Regulatory team based in Gothenburg, Sweden. As Director of Regulatory Affairs, you will be responsible for developing and optimizing systems for tracking regulatory submissions and commitments, and leading the team in managing change controls and submission requirements.About the...

ResponsibilitiesLead a team of specialists in corporate finance, business development, risk analysis, and cash management.Develop and implement financial policies, manage risk, and ensure compliance with regulatory requirements.Support Business Units with working capital financing solutions and structuring, driving negotiations of ISDA agreements.

About the OpportunityWe are excited to offer a unique opportunity for an experienced Cyber Security Consultant to join our team at Knightec.As a Cyber Security Consultant, you will have the chance to work with cutting-edge technology and make a significant impact on the security of our products and services.You will be responsible for implementing EU...

Job DescriptionWe are seeking a highly skilled Medical Device Compliance Specialist to join our team at Randstad - Göteborg. As a key member of our quality assurance department, you will play a crucial role in ensuring the compliance of our medical devices with regulatory requirements.Your primary responsibilities will include:Overseeing quality assurance...

About the OpportunityWe are seeking an experienced Embedded Systems Cybersecurity Specialist to join our team. The ideal candidate will have a strong background in cybersecurity and experience working with embedded systems.The successful candidate will be responsible for developing and implementing comprehensive cybersecurity strategies that address the...

At Prohoc, we're not just building projects – we're creating a safer future for our teams and the communities we serve.Safety and Compliance SpecialistThe Role:Manage and coordinate all safety-related activities on-site to ensure a safe working environment, including risk assessments, safety inspections, audits, and accident investigations.Prepare and...