- Eisai, Inc (Nutley, NJ)
- …through in neurology and oncology, with a strong emphasis on research and development . Our history includes the development of many innovative medicines, notably ... profile, we want to hear from you. The Associate Director (AD), Global Medical Affairs Training and Education is responsible for the planning and execution of Global… more
- L'Oreal (Clark, NJ)
- …that will change people's lives. As a Principal Scientist, Scientific & Regulatory International Affairs (SRIA) Americas in Regulatory Affairs Team you ... Principal Scientist, Scientific & RegulatoryInternational Affairs (SRIA) Americas, L'Oral Research & Innovation -...& regulatory standpoint for US and Americas and at international level. This includes shaping the regulatory environment to… more
- Merck & Co. (Rahway, NJ)
- …and Scientific Affairs (GMSA) (referred to as EDMA) is accountable for the development and execution of scientific & medical affairs plans for their assigned ... skills Preferred Experience and Skills: At least 5 years global or US medical affairs or clinical development experience with proven track record of contribution… more
- Merck & Co. (Upper Gwynedd, PA)
- … Regulatory Compliance, Microbiology, Molecular Microbiology, Pharmaceutical Process Development , Regulatory Affairs Compliance, Regulatory Affairs ... the preparation and submission of CMC dossiers for all assigned development products. -Primary responsibilities include, but are not limited to:Regulatory… more
- Johnson and Johnson (Raynham, MA)
- …practice, dedicated research, or other related training/experience. Experience leading in medical affairs , clinical development , or related roles in research / ... profoundly impact health for humanity. Learn more at https://www.jnj.com Job Function: Medical Affairs Group Job Sub Function: Medical Affairs - MD Job Category:… more
- System One Holdings, LLC (Raritan, NJ)
- …an Integrated Evidence Generation Plan that meets prioritized regional needs *Medical Affairs input into product development and life-cycle management *Worldwide ... Medical Affairs Strategy Team (W-MAST) management * Development and execution of funded medical strategies (advisory boards, pre/post congress meetings, etc.)… more
- Fate Therapeutics, Inc. (San Diego, CA)
- …Therapeutics is looking for an Executive Director or Senior Director in Regulatory Affairs to oversee and direct the strategic planning and execution of clinical ... our corporate headquarters in San Diego, CA. Responsibilities Lead the Regulatory Affairs team in effectively working with internal and external stakeholders to… more
- BioSpace (Indianapolis, IN)
- …pre- and post-commercialization activities by working closely with the Global Medical Affairs , clinical development and brand teams Identify and deliver ... cancer and/or precision medicine expertise preferred Knowledge of drug development and/or medical affairs preferred 5+ years...within your function) Ability to engage in domestic and international travel to the degree necessary to support the… more
- Cleerly (Denver, CO)
- …cardiologists and are a growing team of world-class engineering, operations, medical affairs , marketing, and sales leaders. We raised $223M in Series C funding ... in the job description. About the Opportunity As Principal Regulatory Affairs Specialist, you will provide regulatory support and strategy development… more
- IntePros (Audubon, PA)
- … development teams while following ISO, CE, FDA and international /local regulations. Experience should demonstrate dependability, flexibility and attention to ... IntePros is currently looking for a Regulatory Affairs Associate to join one of our growing... Associate maintains CE Technical Files and registrations for international Regulatory agencies. This position entails working knowledge of… more
- Abbott (Minneapolis, MN)
- …be your true self and live a full life. You'll also have access to: Career development with an international company where you can grow the career you dream of. ... Regulatory area is preferred but may consider quality assurance, research and development /support, scientific affairs , operations, or related area. Note: Higher… more
- Betco Corporation, LTD (Bowling Green, OH)
- …implement and coordinate compliance with federal, state, local and international regulatory requirements applicable to Institution cleaning chemicals, equipment, ... product stewardship. Able to provide technical advice with respect to regulatory affairs to internal team members and our customers. Organize and maintain proper… more
- Lexington Medical (Bedford, MA)
- …worldwide and thrive in a growing company. We are seeking a Senior Regulatory Affairs Specialist to develop, lead and execute a regulatory strategy for new products ... required to align with new regulations and requirements including changes to international standards. Serve as the voice of regulatory on cross-functional teams,… more
- Capstan (Santa Cruz, CA)
- Reports to: Head of Regulatory Affairs (SVP, RA) Workplace type: Hybrid Description: This is a unique opportunity for an experienced Regulatory Affairs ... start-up positioned to revolutionize structural heart care. The Manager of Regulatory Affairs will help build and execute the regulatory strategy for our novel… more
- Stryker (Mahwah, NJ)
- …an FDA regulated industry 2+ years of experience in medical device regulatory affairs Thorough understanding of FDA, Europe, and international medical device ... FL. What you will do As the Senior Regulatory Affairs Specialist , you will support Stryker's Mako and...support Stryker's Mako and Enabling Technology portfolio new product development for both US and OUS Global Regulatory release.… more
- Tandem (San Diego, CA)
- …we're so much more than that. Our company's human-centered approach to design, development , and support delivers innovative products and services for people who use ... more at https://www.tandemdiabetes.com/ A DAY IN THE LIFE: The Sr. Regulatory Affairs Specialist II is responsible for developing strategies for worldwide regulatory… more
- BioSpace (Indianapolis, IN)
- …the world. The Senior Advisor/Director Post approval scientist in Global Regulatory Affairs - CMC commercial solid oral products will use CMC technical knowledge ... timely completion of submission milestones leading to health authoring approval. Development of regulatory strategy and update strategy based upon global regulatory… more
- New York University (Washington, DC)
- …Director of NYU Washington, DC, liaising with the Associate Dean of Academic Affairs for Liberal Studies. This role requires both teaching and administrative work, ... curricular and co-curricular initiatives, and design and implement professional development opportunities for local faculty. Qualifications Required Education: Doctoral… more
- Intuitive (Sunnyvale, CA)
- …Job Description New Product/Indication Submissions Provide regulatory insight to development , new product introduction, and manufacturing teams for assessing the ... filings and compliance. Create awareness within the team regarding international and domestic regulations and product specific standards. Additional responsibilities… more
- Berkeley University of California (Berkeley, CA)
- …at least 80 hours (10 days) of paid time per year to engage in professional development activities. Find out more about how you can grow your career at UC Berkeley. ... and document best practices, offer a variety of methods for professional development , and provide first-class customer service in a cost-effective and transparent… more
