Refine Your Job Search
- Business Analyst - CRM / iPad knowledge Job
- Chemical Operations Specialist
- Compliance Manager- Mahwah, NJ
- Director of Research and Development, Superconducting Materials
- More
- Health Care Specialist
- Information Technology (IT) Quality Validation Analyst Job
- International Regulatory Affairs Specialist
- Manager, Regulatory Affairs
- Medical Assistant (MA)
- Pharma Packaging Manager - Woodbridge, NJ
- Regulatory Compliance Associate
- Senior Clinical Data Analyst Job
- Senior Clinical Database Analyst Job
- Senior QMS Auditor
- Senior Regulatory Affairs Specialist
(1,056 Matches)
Jobs near Avenel, NJ in Science & Biotech
New Brunswick, NJ Take Care Health Systems is currently seeking a confident and outgoing fulltime Medical Assistant to float to variuos Corporate Health Center teams in Central NJ Interact with patients and other physician offices to assist with follow up, appointments,...

Dreaming of a health care career? As a National Guard Health Care Specialist, you will address the health care needs of civilians after natural disasters or civil emergencies. You will also be the first line of defense against injuries and illnesses suffered by our Soldiers...

Yoh has a contract opportunity for a Business Analyst with CRM / iPad experience to join the team in Bridgewater, NJ . Job Responsibilities: - Lead and participate in requirements gathering sessions with client business and IT personnel: - Plan, conduct, document, and...

As an Army National Guard Chemical Operations Specialist, you'll be there and prepared whenever a community is flooded, an earthquake shakes the foundations of a city, a hurricane makes landfall, or an enemy uses biological or chemical warfare. You will know what to do to...
Job Summary: Interface with Spine international RA affiliates to: Plan, organize, and implement strategies and activities required to procure regulatory approval for new and revised product lines in all target markets. Ensure compliance to all international affiliates...
Plan, organize and implement strategies and activities required to procure regulatory approval for new and revised product lines. Ensure compliance with all US, EU and SO international requirements and corporate policies and procedures regarding submissions for market...

Yoh has a contract opportunity for a IT Quality Validation Analyst / Technical Writer to join our client in the Park Ridge, NJ area. Job Responsibilities: - Prepare computer validation documents such as Validation Plans, User Requirements, Configuration Specifications, Test...

Yoh has a contract opportunity for a Senior Clinical Database Analyst (EDC) to join our client in the Park Ridge, NJ area. Job Responsibilities: - Provide programming and technical support related to clinical trials, end users support and troubleshooting using different...

Yoh has a contract opportunity for a Senior Clinical Data Analyst (SAS) to join our client in the Park Ridge, NJ area. Job Responsibilities: - Perform SAS programming to provide data review complex listings/reports to support Data Management function Oncology trials. -...
Evaluate complaints to determine if MDR/MDV reports are required to FDA and Competent Authorities. Review reports of customer complaints and assess them for MDR / MDV reportability to FDA / Competent Authorities. Ensure reports to FDA / Competent Authorities are completed...
Work closely with members of Stryker Performance Solutions leadership and the divisional Compliance Committee to ensure effective management of key components of the Compliance Program: knowledge of applicable laws & standards, education & training, monitoring & auditing,...
Lead internal quality management system audits to 21CFR 820, ISO 13485:2003, 93/42/EEC and other applicable Standards to determine whether the quality management system is in compliance with established requirements and to evaluate its effectiveness. Create formal audit...
Oversee the process of preparing product submissions to domestic and international regulatory bodies and manage process from inception to approval. Establish and implement global regulatory strategies with cross-functional teams to assure compliance and approval. Ensure...
Oxford Superconducting Technology (OST) has an outstanding opportunity for a Director of Research and Development to join our management team. Reporting to the General...
Pharma Packaging Manager - Woodbridge, NJ
3 Days Ago
Oversee multiple shifts while assuring compliance with GMP, corporate and other regulatory standards for quality and safety. Requirements: ** BA or BS degree. ** 5+ years in...
14,778 New Jobs
Posted Last Week!
Posted Last Week!
Create an account
to have the right ones for you delivered right to your home page, every day.