- Atlantic Health System (Morristown, NJ)
- …reports and documents all adverse events and serious adverse events per regulatory requirements, sponsor requirements and policies and procedures. + Writes study ... according to good clinical practices in research records. Maintains study drug/ device accountability records as required. Completes required case report forms in… more
- J&J Family of Companies (Raritan, NJ)
- …Bachelor (Rising Juniors or above), Masters, and PhD who desire a career in the medical device or pharmaceutical industry and are eager to learn technical and ... or PhD in life science, analytical science, data science, regulatory compliance or regulatory affairs, computer science,...to participate in Company employee benefit programs such as medical insurance, sick time, holiday pay, and the Company's… more
- Bristol Myers Squibb (Princeton, NJ)
- …of industry experience in bioanalysis and/or IVD/CDx development within pharmaceutical, biotech, medical device , or CRO settings. + Direct experience managing ... supports resource and budget planning, and ensures adherence to regulatory standards (GLP, CLIA, CAP, ISO13485, 21 CFR Part...plans then in effect and may include the following: Medical , pharmacy, dental and vision care. Wellbeing support such… more
- Kelly Services (Somerset, NJ)
- …systems or applications support within a regulated industry (pharmaceutical, biotech, or medical device ). + Experience with system validation and compliance ... quality-related software tools are effectively implemented and aligned with regulatory requirements and business needs. The engineer collaborates with… more
- Merck (Rahway, NJ)
- …distribution/ transportation technologies for pharmaceutical products including parenteral and/or medical device and combination products. + Demonstrated ... and 3rd party logistics sites, supply chain and technology teams, and regulatory and project leaders. The successful candidate will demonstrate ownership and make… more
- Sokol Materials & Services (Skillman, NJ)
- …interest in pursuing a career in CQV within the pharmaceutical, biotechnology, or medical device industries. + Excellent organizational skills and attention to ... service providers, you will ensure that critical CQV activities align with regulatory standards and best practices. This role requires a professional with analytical… more
- Integra LifeSciences (Princeton, NJ)
- …with substantial experience supporting international business activities. Pharmaceutical or medical device industry experience preferred; + Comfort navigating ... in multiple jurisdictions and under a variety of complex legal and regulatory schemes; + Collaborating with the compliance team to ensure Integra's business,… more
- Norstella (Trenton, NJ)
- … and commercial intelligence solutions and services for the Pharmaceutical, Biotech/ Medical Device , Financial and Professional Services sectors. Our data ... as the industry's gold standard to drive clinical, commercial and regulatory -related decisions and create real-world opportunities for growth. We deliver timely… more
- Integra LifeSciences (Princeton, NJ)
- …of medical devices in conformance with the Quality System Regulation, ISO 13485, Medical Device Directive, ISO 14971, IEC 60601 and other regulatory ... improve processes and procedures. + Collaborate with External Manufacturers during regulatory audits and inspections. + Support Supplier Quality projects and issues… more
- Stryker (Trenton, NJ)
- …technology or pharmaceuticals. + 8+ years of experience in clinical data management, in medical device /pharma industry is required with a Master's degree or 10+ ... in alignment with quality standards, ICH guidelines, GCP, and regulatory requirements. This includes establishing and maintaining clinical trial databases,… more