Position: Senior Scientific and Regulatory Affairs Manager II Intertek Scientific and Regulatory Consultancy Group is looking for a motivated and client focused senior regulatory affairs professional who is seeking an opportunity to be a Program Manager to promote our food, nutrition
At Horizon Therapeutics, we define success by the number of lives touched, lives changed, and lives saved. Our global biotechnology company is made up of agile, out-of-the-box thinkers with a focus on delivering breakthrough medicines to
RTI International seeks an experienced human subject’s protection professional to join the RTI Office of Research Protection as an IRB Administrator/Coordinator. The Office of Research Protection is responsible for ensuring compliance with all regulations related to
The National Association of Community Health Centers (NACHC) is the national membership organization for federally qualified health centers (FQHCs). Health centers deliver comprehensive, culturally competent, high-quality primary health care services to the nation’s most vulnerable individuals
Job Description Job Title: Regulatory Affairs Specialist 3 How will you make an impact? As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues
Job Description Company overview Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $35 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer.
Job Description Our client, a leading medical device company, is currently seeking an accomplished Senior Regulatory Affairs Specialist to join the team. Here is an overview of the role: 1) Maintain technical files and technical documentation in compliance
Research Internships at Microsoft provide a dynamic environment for research careers with a network of world-class research labs led by globally-recognized scientists and engineers. Our researchers and engineers pursue innovation in a range of scientific and
The Senior Director, CMC Regulatory Affairs reports to the VP, Regulatory Affairs and develops and executes CMC regulatory strategies and activities. This includes oversight of the development and implementation of global regulatory strategies, ensuring timely preparation, review and submission of CMC documents
For years, Abbott’s medical device businesses have offered technologies that are faster, more effective, and less invasive. Whether it’s glucose monitoring system, innovative therapies for treating heart disease, or products that help people with chronic pain
About Dexcom Founded in 1999, Dexcom, Inc. provides continuous glucose monitoring technology to help patients and their clinicians better manage diabetes. Since our inception, we have focused on better outcomes for patients, caregivers, and clinicians by
Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to
Job Description Summary Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it’s no small
About us At Cooper University Health Care, our commitment to providing extraordinary health care begins with our team. Our extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies
The Associate Director, Regulatory Affairs will be responsible for providing all aspects of regulatory support for supplemental indications associated with an approved Neurology or Oncology agent. In addition, this position will serve as the lead supRegulatory Affairs, Director, Associate, Regulatory, Monitoring,
Our client, a leading medical devices company, is looking for a Regulatory Affairs Coordinator. This is for an initial duration of 8 months and is located in Franklin Lakes, NJ. This is a Hybrid – 3 days onsite
Monitor, interpret, distribute, track, and assess new State regulatory guidance (including all guidance documents, memos, administrative directives relative to all commercial compliance/regulatory communications. Ensure that most recent contract changes are reflected on departmental policies and process by monitoring
Independently authors, compiles, reviews, schedules, and submits high-quality regulatory submissions in adherence with technical document standards that are fully compliant with FDA and ICH requirements within company timelines. Plans, coordinates anRegulatory Affairs, Regulatory, Associate, Senior, Operations, Business Services...
This function will primarily providing labeling support to the U.S. Regulatory Affairs office (Mahwah, NJ). This function is to oversee a full portfolio of ANDA products for both approved and unapproved AND - As. The successful candidate might
Here, we provide our RA/ QA team the opportunity to learn new things, as well as endless growth opportunities If you are interested in working at one of the Worlds Best Workplaces,Regulatory Affairs, Specialist, Staff, Regulatory, Manufacturing, Business Services...
