Regulatory Compliance Associate

Job Overview: Meet is seeking an experienced Regulatory Compliance Engineer to join our team. As a Senior Quality Engineer, you will be responsible for ensuring the compliance of our medical devices with regulatory standards.Responsibilities:Deliver engineering expertise in Quality Assurance, Design Controls, Risk Management, and Statistical Techniques.Drive...

Job DescriptionJob DescriptionJob Summary:Manage international regulatory submissions, registrations, and compliance, ensuring timely coordination and project management within the medical device industry.Job Requirements:Minimum 3 years of direct experience in international registration4-5 years as an independent Regulatory Affairs (RA) specialist in...

Job DescriptionAs a Manufacturing Technician II or III, you will be responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines, and any other related regulations.You will work under the general direction of the lead technician and the overall direction of the supervisor, ensuring...

About MeetMeet is a leading developer of innovative medical devices. We are seeking a talented Senior Quality Engineer to join our team.Job OverviewAs a Senior Quality Engineer at Meet, you will be responsible for ensuring the quality and compliance of our products. You will work closely with cross-functional teams to develop and implement quality assurance...

About OrthofixAt Orthofix, we are guided by our organizational values of Take Ownership, Innovate Boldly, and Win Together. We collaborate closely with world-class surgeons and other partners to improve people's quality of life. Our global team of over 1,600 employees brings to market highly innovative, cost-effective, and user-friendly medical technologies...

About PrideStaff: PrideStaff is a national staffing organization delivering innovative solutions to the challenges employers face every day. We've been a consistent industry leader, developing technology and service processes that allow us to deliver superior performance. With locations across the United States, we're well-positioned to partner with clients...

Job Title: Senior Regulatory Affairs SpecialistCompany OverviewEntegee is a leading provider of custom automation solutions, specializing in controls and robotic technologies worldwide.We are seeking an experienced Senior Regulatory Affairs Specialist to join our team. This role will be responsible for ensuring compliance with international regulatory...

A growing medical device company based in North San Diego county is hiring a Regulatory Affairs Manager for their QA/RA department. The company is developing breakthrough products for the treatment of cardiac arrhythmias and will be commercializing several new products by the end of this year and early next.The RA Manager will be responsible for leading the...

A growing medical device company based in North San Diego county is hiring a Regulatory Affairs Manager for their QA/RA department. The company is developing breakthrough products for the treatment of cardiac arrhythmias and will be commercializing several new products by the end of this year and early next.The RA Manager will be responsible for leading the...

About the RolePangea Biological is seeking a Regulatory Monitoring Coordinator to oversee environmental compliance on construction projects across Southern California. As a key member of our team, you will work closely with project teams, landowners, clients, and construction personnel to ensure seamless project execution.Your responsibilities will include...

About the RoleWe are looking for a talented Regulatory Affairs Specialist to join our team at Carlsmed.In this role, you will work closely with cross-functional teams to provide essential regulatory input during product development, submissions, and post-market surveillance activities.You will also be responsible for reviewing promotional marketing materials...

Job OverviewAt Lifelancer, we are seeking a skilled Regulatory Medical Writer to join our team. As a key member of our regulatory writing department, you will play a crucial role in preparing and managing clinical regulatory documents for submission to regulatory agencies.About the CompanyLifelancer is a leading talent-hiring platform connecting...

Job DescriptionWe are seeking a highly skilled Project Compliance Manager to spearhead quality control efforts in line with company policies and contractual obligations.Primary ResponsibilitiesGain in-depth knowledge of corporate quality control programs, company standards, and regulatory requirements.Collaborate with project teams to establish and maintain...

We are seeking a skilled Clinical Research Associate to join our team at Della Infotech. The ideal candidate will have a strong background in biology, chemistry, or bio-engineering and excellent knowledge of Good Clinical Practices (GCP). In this role, you will be responsible for coordinating and conducting clinical research studies for in vitro diagnostics,...

At Alphatec Spine, Inc., we are committed to delivering high-quality medical devices that meet the needs of our customers. We are seeking a highly skilled Product Validation and Compliance Expert to join our team and ensure the quality and safety of our products.This role involves assessing incoming inspection methods and sampling, process controls at...

**Job Overview**We are seeking a highly motivated Clinical Research Associate to join our Regulatory and Clinical Affairs organization at Della Infotech. As a key member of our team, you will play a critical role in ensuring the quality of FDA submissions and securing necessary approvals for our products.The successful candidate will have a strong background...

Key ResponsibilitiesThe successful Regulatory Affairs Specialist will be responsible for:Writing and submitting 510(k)s and interacting with the FDA during the review processPreparing software documentation in support of 510(k)s, such as software development plans, protocols, and reportsParticipating in Design Control and Risk Management processes for...

About ViasatWe are a global company shaping how consumers, businesses, governments and militaries around the globe communicate. Our mission is to deliver connections with the capacity to change the world.Job SummaryViasat seeks an Associate Manager, International Tax to join our Tax team. This role will be heavily involved in all aspects of US international...

Job OverviewLHH Recruitment Solutions is partnering with a stable organization to hire a detail-oriented and organized Payroll Specialist to manage and process payroll for all employees, ensuring compliance with federal, state, and local regulations.This role requires handling sensitive information with discretion and accuracy. Estimated salary for this...

About the RoleWe are seeking a highly skilled Clinical Research Associate to join our team at IQVIA. As a Clinical Research Associate, you will be responsible for designing, planning, coordinating, and conducting all activities involved in initiating, monitoring, and completing clinical research studies for in vitro diagnostics.This role includes ensuring...