Regulatory Affairs Specialist

As a Regulatory Affairs Quality Specialist at Lifelancer, you will play a pivotal role in maintaining and improving certifications such as ISO 13485, MDSAP, and CE mark. This position requires ensuring compliance with other relevant standards and regulations while collaborating with the Regulatory Affairs and Quality Manager to integrate regulatory...

We are seeking an experienced Regulatory Affairs Quality Specialist to join our team at Lifelancer, a leading talent-hiring platform in Life Sciences, Pharma, and IT. This role is based in the United States and offers a competitive salary of $85,000 - $110,000 per year, depending on experience.Job DescriptionThe Regulatory Affairs Quality Specialist will...

Job Title: Regulatory Affairs Quality Specialist PositionCompany OverviewAt Intelerad, we are committed to providing innovative medical imaging software solutions that revolutionize healthcare. With over 20 years of experience and a global presence across 11 time zones, our team is dedicated to delivering cutting-edge technology that makes a real difference...

About ProPharma GroupProPharma Group is the leading global, independent, single-source provider of regulatory, clinical, and compliance services serving pharmaceutical, biotechnology, and medical device companies. Our team of experts brings a comprehensive portfolio of regulatory sciences, clinical research solutions, life science consulting, RD technology,...

At Disability Solutions, we're dedicated to fostering a culture of growth and collaboration. As an Assistant General Counsel, you'll play a vital role in shaping our company's regulatory affairs strategy.About the Role:Collaborate with commercial business functions and management to provide proactive legal advice on issues related to pharmaceuticals and...

About the JobThis Financial Regulatory Specialist position is ideal for individuals with a passion for finance and regulatory compliance. The successful candidate will have strong analytical skills and be able to communicate effectively with internal stakeholders.

Job OverviewWe are seeking a highly skilled Senior Medical Regulatory Consultant to join our team in Raleigh, NC. As a key member of our promotional review committee, you will be responsible for providing compliant and scientifically sound solutions to support the launch and growth of our clients' pharmaceutical products.About the RoleThis is a full-time...

Overview:This role offers a unique blend of analysis, compliance, and business acumen. As a Regulatory Risk Specialist, you will play a critical part in ensuring the integrity of Bank operations.Key Responsibilities:• Data Analysis: You will source, validate, and interpret data to identify discrepancies and risks. Your analytical skills will be essential...

Key ResponsibilitiesYou will support the development of local medical education activities, providing guidance on topics and speaker suggestions to support the full Merz Aesthetics portfolio.Assume responsibility in case of adverse events (internal & external) according to the Merz Group Standard Operating Procedures.You will also be responsible for the...

About the RoleAs a Medical Affairs Specialist at Merz Aesthetics, you will play a crucial role in supporting the overall distribution partner business medical-marketing-sales strategy. Your primary responsibility will be to provide scientific, medical, and clinical information regarding our product portfolio and its safe and effective use to healthcare...

Job DescriptionThis position provides support to the Associate Dean for Faculty and Academic Affairs in the College of Education at North Carolina State University. The successful candidate will interact daily with the Associate Dean to coordinate, solve problems, execute tasks, and provide administrative assistance.Key Responsibilities:Coordinate with the...

About the RoleWe are seeking a highly skilled Biocompatibility / Toxicology Expert to join our team. In this role, you will be responsible for evaluating the biological safety and performance of Class III Absorbable Medical Devices for Aesthetics purpose.Main Responsibilities1. Develop and implement biological evaluation plans and reports for...

Job DescriptionThe role of the Sr. Compliance Specialist is a critical position within Indivior PLC, supporting the company's commitment to maintaining high-quality standards in pharmaceutical manufacturing. Located in Raleigh, NC, this position offers an exciting opportunity for individuals passionate about compliance and regulatory affairs to contribute to...

Overview: Booth & Associates LLC is seeking a highly skilled Permitting Lead to join our team. In this role, you will be responsible for ensuring compliance with local, state, and federal regulations related to permitting, zoning, and building codes.Key Responsibilities:Develop and implement permit acquisition plans for projectsReview and interpret local,...

Job Title: Biocompatibility/Toxicology ExpertOverview of the Position: We are seeking a highly skilled Biocompatibility/Toxicology Expert to join our team at The Accuro Group. As a key member of our Regulatory Affairs department, you will be responsible for ensuring the safety and performance of our medical devices.Estimated Salary Range: $140,000 - $180,000...

About the RoleThis position involves working closely with Regulatory Affairs, Clinical teams, and Production sites to ensure compliance with regulatory standards and guidelines. As a Biocompatibility Expert, you will be responsible for evaluating the biological safety of medical devices and ensuring that they meet the required...

Key ResponsibilitiesThis Biocompatibility / Toxicology Expert role involves:1. Preparing biological evaluation plans and reports for projects/devices.2. Coordinating preclinical programs to evaluate and demonstrate the safety and performance of medical devices in accordance with regulatory requirements (incl. EU MDR, US FDA, Chinese Regulations) and internal...

Job OverviewThe Biocompatibility / Toxicology Expert will support the Biocompatibility Team to ensure the evaluation of biological safety and performance of Class III Absorbable Medical Devices for Aesthetics purpose. This role requires a deep understanding of biological evaluation standards, such as the ISO 10993 series.Main Responsibilities1. Preparation...

Job DescriptionWe are seeking an experienced Medical Affairs Specialist to support our overall distribution partner business medical-marketing-sales strategy. As a key member of our team, you will be responsible for providing scientific, medical and clinical information regarding our product portfolio and its safe and effective use to healthcare...

Job DescriptionWe are looking for a highly skilled Senior Medical Advisor - Global Clinical Trials to join our team at Lifelancer. As a key member of our organization, you will provide medical oversight of global clinical trials, collaborate with cross-functional teams, and communicate effectively with clients, investigators, and project team members. If you...