Regulatory Affairs Specialist

Covestro is seeking to hire an Environmental and Regulatory Affairs Specialist for our New Martinsville, WV production site. This position will be responsible for developing, implementing and administering environmental compliance programs for the Ne Regulatory Affairs, Environmental, Specialist, Regulatory, Manufacturing, Business Services

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...

Job Title: Senior Regulatory Affairs Specialist Duration: 9 months Location: Irvine, CA (Onsite) Shift: 8 am to 5 pm. Our Client is a Global medical device Manufacturer. We are looking for a Senior Regulatory Affairs Specialist to complete and maintain regulatory approvals and clearances of assigned products. Create regulatory submissions (exercising...

Regulatory Affairs Regulatory Affairs SME Compensation: $110,000 to $130,000 Location: Shelbyville, IN ABOUT OUR CLIENT: Our client is a leader in their space, in SE Indianapolis. Their state-of-the-art facility will be where groundbreaking ideas become reality. Their contracts unrelated to automotive will provide long term stability. As a leading player in...

Job Title: Regulatory Affairs Manager I Career Level - D Introduction to role: Join our dynamic Biopharmaceuticals R&D team as a Regulatory Affairs Manager I. This role is a unique opportunity for a regulatory specialist with project management capabilities to lead the end-to-end planning, coordination, and execution of assigned deliverables. You will be...

Overview: Undergraduate or Graduate student in a Science discipline.  This individual will work in our Regulatory Affairs Department, supporting the Regulatory Strategy group.  He/she will be assigned interesting and challenging projects related to competitive data research, precedent analysis, regulatory environment monitoring and ad hoc projects. ...

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...

We are partnering with an exciting oncology biotech that is looking for an accomplished Director of Regulatory Affairs Strategy to lead within their Regulatory Affairs team. The ideal candidate will be responsible for developing and executing regulatory strategies that drive the successful development, registration, and commercialization of products in their...

Responsibilities: Essential Duties Plans and prepares registration documents for marketing approval of drug and device products in the US and in foreign countries. Serves as a regulatory liaison for new product development and make regulatory assessments of proposed changes to existing products for impact to regulatory documentation. Provides strategic input...

Role : Sr Spec, Regulatory Affairs Location : Irvine, CA - 92606 Duration : 9+ Months on W2 Job Description: Key Responsibilities: • Create regulatory submissions (exercising judgment to protect proprietary information) for finalization and submission by OUS EW affiliates; track timelines and document milestone achievements, participate in developing...

Overview: Director of Compliance and Regulatory Affairs Overview   The primary function of this position is to direct and provide oversight of Somnia’s Compliance and Regulatory Affairs Program.  The individual will be responsible for planning, implementing, and managing a compliance and regulatory affairs program for Somnia and its affiliated...

Are you passionate about revolutionizing healthcare through innovative medical devices and cutting-edge AI technology? We are seeking a dynamic and experienced Director of Regulatory Affairs to join our team in the vibrant San Francisco Bay Area. If you thrive in a fast-paced environment, are driven by challenges, and are eager to make a significant impact...

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...

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...

Job Description Position: Director, Regulatory Affairs Strategy Location: New York City, NY (Remote) Overview: The Director of Regulatory Affairs Strategy will take a lead role in crafting and executing global and regional regulatory strategies for a range of projects and products. The incumbent will collaborate with various internal teams, maintain vital...

About Our Client: Our client revolutionizes patient care with cutting-edge hydrogel-based medical devices. Their commitment to self-funding projects, strategic partnerships, and innovative technology positions them as leaders in addressing unmet medical needs. With over ten spin-off companies and a $4B value, their impact has positively affected over 5...

Essential Duties 1. Functions as the primary source of expertise to ensure that proposals meet sponsor requirements, regulatory compliance requirements, University, School, Federal, and State policies and regulations governing sponsored research, and that proposals are submitted correctly and per appropriate deadlines.2. Understands and interprets grant...

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...