Are you a business? Hire regulatory specialist candidates in Passaic, NJ
Also ensure that additional regulatory practices are in line with local, state, and federal laws. Point of internal contact for customer inquiries regarding product regulatory compliance matters. Be prepared to assist customers and the Emergency Response team by maintaining and providing technica...
As a Regulatory Affairs Specialist, your role will be to coordinate, prepare, and review regulatory documents/certifications required for both domestic and international projects. Job Title: Regulatory Affairs Specialist. Your role will also involve supporting the development of Regulatory Specif...
Reporting to the Regional Vice President of Government Relations, you will have substantial contact with state regulatory officials on the timely approval and implementation of ISO filings, and related issues. Timely approval and implementation of ISO's regulatory filings of insurance program cov...
Catalent Pharma Solutions in Somerset, NJ is hiring a Senior Regulatory and Compliance Specialist for the Compliance Group. The Senior Regulatory and Compliance Specialist candidate must be knowledgeable in global regulations pertaining to the pharmaceutical industry and their impact on manufactu...
Represent international RA and demonstrate leadership in complex product development strategies by identifying and interpreting relevant regulatory requirements, and providing actionable regulatory guidance throughout the product development cycle prior to regulatory submission. Review protocols ...
Senior Quality Systems Specialist (Regulatory). Supplier Quality Regulatory Affairs. As a Quality System Specialist, you will act as the primary focal to interface with Boeing Suppliers, Business Partners and the Federal Aviation Administration on various complex Quality Management System related...
This role will serve as a regulatory liaison to internal and external investigators, sponsors, collaborating divisions, departments and institutions, and Institutional Review Boards (IRBs), Data Safety and Monitoring Boards, Biosafety committees, Laboratory facilities, and external regulatory age...
Administer regulatory change program review of vendor tools/applications available for regulatory change monitoring oversee selection/implementation/administration of vendor tool/application if warranted summarize and distribute new/amended rule proposals and rules to internal constituents overse...
Also ensure that additional regulatory practices are in line with local, state, and federal laws. Specific Responsibilities:*Primary coordinator for TSCA/DSL compliance in North America*Prepare all PMN, LVE, and NOC submissions*Point of internal contact for customer inquiries regarding product re...
We are seeking a talented Technical Writer to join our team at a leading financial institution. As a Technical Writer specializing in IT Network Documentation, you will be responsible for creating clear, concise, and accurate documentation for our network infrastructure and related systems. Prove...
Job Title: IT Project Manager / Risk Manager (Technical and Infrastructure). IT project management, Project management, Infrastructure, Risk management, Vulnerability assessment, Vulnerability Remediation, Cloud, DevOps. Looking for someone with Project Management experience (Infrastructure / Tec...
Conduct regular assessments to evaluate the effectiveness of IT controls and identify areas of non-compliance with SOX IT general controls, PCI-DSS, and GDPR. Collaborate with cross-functional teams to develop and implement processes and controls to ensure compliance with regulatory requirements....
Title :: Infrastructure Project Manager (Need financial Experiences). Experience with governance, risk, and compliance projects and program oversight. ...
Our client, an exciting and growing Biotech Company, is seeking a Regulatory Affairs professional at the Senior Director level. Launch the company's regulatory strategy having leadership over all regulatory activities. This role will lead the North America regulatory strategy and work extremely c...
My client is a multinational CDMO looking for a Regulatory Affairs Manager to work with the FDA and their client sites to manufacture generic APIs, drug products, and certain med devices. Looking for a unique approach to Regulatory Affairs? Want to push boundaries and bring life-saving medicine t...
Events and Program Administration Manager. ...
Job Summary: We are seeking a highly skilled and experienced Technical Program Manager who will take on the role of a program management for a very large programs to build a complete new application in Pharmaceutical manufacturing Industry Area. Proven experience as a Client Engagement Manager, E...
Job Title: BA Technical writer. Technical Writer with Business Analysis experience relating to Trading System. Ability to understand and explain technical concepts. ...
Associate Director/Director, Regulatory Affairs (Oncology). They are looking for an Associate Director or Director of Regulatory Strategy to join their team. This role will be reporting into the VP of Regulatory Affairs and will be serving as the Lead for a US Phase III Oncology program. Serve as...
TSCA/Environmental Specialist * Lyndhurst, NJ, USA Company Description With over 100 years of ... Also ensure that additional regulatory practices are in line with local, state, and federal laws
Job Description Compliance Specialist Summary Description Reporting to the Assistant Director of ... Act as assistant researcher regarding compliance and regulatory program standards and requirements ...
The Academic and Compliance Specialist (ACS) leads and coordinates the development of new academic programs and ensures regulatory compliance with State and accreditation standards and procedures
