Environmental and Regulatory Affairs Specialist

Our customer is looking for a Senior Regulatory Affairs Specialist to join a team of 7 and supporting the product submissions, regulatory guidance, and registering products. Duties Include: Maintain and establish regulatory functions for medical device and environmental compliance. Uphold Quality Management System for domestic and international...

Regulatory Affairs Specialist Jobs (Found 1 Job) Nationwide and Remote jobs are not shownOverviewThe Regulatory Affairs Coordinator will integrate with the RA team and provide general support as needed under the guidance of RA colleagues. This is an exciting opportunity with potential for...#J-18808-Ljbffr by Jobble

Regulatory Affairs Specialist Jobs (Found 1 Job) Nationwide and Remote jobs are not shown OverviewThe Regulatory Affairs Coordinator will integrate with the RA team and provide general support as needed under the guidance of RA colleagues. This is an exciting opportunity with potential for... #J-18808-Ljbffr

Job Description One of our top clients is recruiting again! They are looking for a Regulatory Affairs Specialist for their facility. Interested job seekers should have work experience with a highly successful and well-established medical device manufacturer. An overview of the Regulatory Affairs Specialist's responsibilities: 1) Be responsible for...

We believe that great healthcare is an essential safeguard of human dignity. At Laborie, we know the work we do matters – it’s what fuels our motivation and contributes to our success. If you’re ready to make a positive impact in the lives of patients across the globe, we’d like to meet you. We support and empower our employees to grow their careers...

My client are looking for a Regulatory Affairs Specialist with experience in Asia Pacific Product Registrations. You MUST be willing to work hybrid in office at Exton, Pennsylvania. Essential Duties and Responsibilities: Author and review China, South Korea, Japan and additional submissions as well as US and EU Submissions Work cross functionally with...

**Empower. Unite. Care.**: **MetroPlusHealth** is committed to empowering New Yorkers by uniting communities through care. We believe that Health care is a right, not a privilege. If you have compassion and a collaborative spirit, work with us. You can come to work being proud of what you do every day. **About NYC Health + Hospitals**: MetroPlus**Health...

Job DescriptionJob DescriptionImagine working for a company that knows their employees are the key to its success, a company that provides exceptional results while being environmentally conscious and ahead of the curve in research and development; MicroCare LLC is that company. Since 1983, we have been a trusted global provider of critical cleaning...

· 0-2 years of experience in regulatory affairs, and/or experience in QA, R&D, Manufacturing or Project Management within the IVD industry · Working knowledge of FDA, and CE marking requirements for IVD products is a plus · Able to work independently and with others · Able to work with minimal supervision · Excellent computer applications skills ·...

Empower. Unite. Care.MetroPlusHealth is committed to empowering New Yorkers by uniting communities through care. We believe that Health care is a right, not a privilege. If you have compassion and a collaborative spirit, work with us. You can come to work being proud of what you do every day.About NYC Health + HospitalsMetroPlusHealth provides the highest...

Regulatory Affairs Consultant Cambridge MA, Remote with occasional site time Medical Device 6 month contract - 40 hours per week Competitve hourly rate A MedTech company based in Massachusetts specializing in Class 2 Medical Device solutions are looking to hire a contractor for a 6-month renewable contract to support with product submissions in multiple...

About us: BeZero Carbon's mission is to scale investment in environmental markets that deliver a sustainable future. We are a carbon ratings agency. We equip world-leading organisations with the knowledge, tools and confidence to make better climate decisions. BeZero Carbon is the largest global ratings agency for the Voluntary Carbon Market. We are driving...

Summary: The Regulatory Affairs team is responsible for coordinating and facilitating communications between the Bank and its various regulators on behalf of all US business operations and entities, as well as for coordinating the regulatory remediation efforts within the region. The team is primarily responsible for all interaction with regulatory agencies...

Job DescriptionJob DescriptionScismic is supporting the growth of a late-stage, publicly traded biopharmaceutical company developing targeted radiotherapies to deliver cancer-killing radiation with cellular level precision to treat patients with high unmet medical needs.  Their vision is to build a specialty, hospital-focused radiotherapeutics company that...

Job DescriptionJob DescriptionScismic is supporting the growth of a late-stage, publicly traded biopharmaceutical company developing targeted radiotherapies to deliver cancer-killing radiation with cellular level precision to treat patients with high unmet medical needs.  Their vision is to build a specialty, hospital-focused radiotherapeutics company that...

At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation – ultimately providing employees with the opportunity to work across teams, functions and even the globe. Recognizing the importance of individualized flexibility, our ways of working allow employees to balance personal...

About Our Client Our client is a large, foreign, International Bank. With its full-fledged services, our client specializes in corporate lending, international trade services, treasury business, U.S. dollar clearing, retail banking, correspondent banking and various other lines of business. Job Description Reporting into the Head of Regulatory Affairs and...

Lead the regulatory efforts for IND-enabling activities, including the preparation of the Investigational New Drug (IND) application for our groundbreaking oncology and CNS therapies targeted for submission this year and early next.Be the go for all things regulatory and acting as a key voice to the future of all trials, SOPs and strategy for these early...

Lead the regulatory efforts for IND-enabling activities, including the preparation of the Investigational New Drug (IND) application for our groundbreaking oncology and CNS therapies targeted for submission this year and early next.Be the go for all things regulatory and acting as a key voice to the future of all trials, SOPs and strategy for these early...

Lead the regulatory efforts for IND-enabling activities, including the preparation of the Investigational New Drug (IND) application for our groundbreaking oncology and CNS therapies targeted for submission this year and early next.Be the go for all things regulatory and acting as a key voice to the future of all trials, SOPs and strategy for these early...