- Kelly Services (Bridgewater, NJ)
- …**egulatory Affairs Specialist ** Kelly(R) Science & Clinical is seeking a Regulatory Affairs Specialist for our client a leading medical device ... **HYBRID role - 3 days in the office** **Overview** Responsible for providing Regulatory Affairs support to International RA Teams for product registrations,… more
- Astrix Technology (New Brunswick, NJ)
- **Environmental Health & Safety Specialist ** Regulatory Affairs Middlesex County, NJ, US Pay Rate Low: 75000 | Pay Rate High: 85000 + Added - 03/12/2024 ... Apply for Job _Join our team as an Environmental Health & Safety Specialist for a leading bioscience organization!_ _As an Environmental Health & Safety … more
- AbbVie (Florham Park, NJ)
- …level will be determined by the qualifications listed below. Purpose Provides specialist medical and scientific strategic and operational input into core medical ... affairs activities such as: healthcare professional/provider interactions (HCPs, Patients...into and influences the development of asset strategy. Provides specialist medical insights, and executes on data generation, communication,… more
- ThermoFisher Scientific (Bridgewater, NJ)
- …Education A Bachelor's degree or equivalent experience in Environmental Science, Chemistry, Regulatory Affairs , Industrial Safety, or a related field is ... regulations and appropriate qualifications. + Certification in hazardous materials handling or regulatory affairs is a plus. **Knowledge, Skills, Abilities** +… more
- ManpowerGroup (Wayne, NJ)
- …of three years of experience with medical devices or pharmaceuticals in a Quality, Regulatory Affairs , or Regulatory Compliance role. + Working knowledge of ... Our client, a leader in the medical device industry, is seeking a Quality Compliance Specialist to join their team. As a Quality Compliance Specialist , you will… more
- Hackensack Meridian Health (Edison, NJ)
- …+ Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related experience in the field ... compliant study conduct according to all relevant local, federal, and state regulatory and institutional Polices and Standard Operating Procedures. This role carries… more
- Sanofi Group (Morristown, NJ)
- …the clinical data. + Interact with relevant teams Innovation, Regulatory , Pharmacovigilance, Evidence generation (eg biostatisticians, Medical Writers, Monitoring ... team, eDS, etc.), Scientific Affairs and Growth (eg Marketing representatives when relevant). Common...part of the CTD; Ensure the eDS (electronic Document Specialist ) is involved in the project at an early… more