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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...
HSES Regulatory Specialist - Product Stewardship**. Located in Branchburg, NJ Intitul du poste HSES Regulatory Specialist - Product Stewardship Type de contrat CDI / Permanent Date de publication 2021-04-14 Pays Etats-Unis d'Amrique Company presentation. Creates and maintains ...
Responsibilities include managing the entire contract development lifecycle, as well as ensuring corporate regulatory and license compliance requirements are met. ...
Responsible for the coordination and preparation of document packages for regulatory submissions from all areas of the Company. Keeps abreast of regulatory procedures and changes. Coordinates the collection of documents, records, reports, and data from the Development, Clinical Affairs, Quality, ...
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...
Prepare new and maintain existing regulatory files in accordance with regional requirements, including but not limited to document updates, management of regulatory information in databases, and navigating document control systems. Review regulatory content for completeness, accuracy, consistency...
Assesses regulatory pathways for new products, product modifications or product conversions; develops regulatory strategies and planning for submissions or support of customers’ regulatory submissions. Acts as a RA Core team Member (RA CTM) and works with RA Manager and Platform Leaders to ensure...
Eligibilities & qualifications....
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...
FRAGRANCE REGULATORY SPECIALIST. Communicate with affiliate SRA teams on safety and regulatory issues. Lead supplier communication on requests for new/ updated safety/regulatory information. Maintain and update global regulatory database (T-Check). ...
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Project ManagerLocation: Paramus, NJ (Hybrid)Duration: 6+ MonthsPay Range: $60/hr to $65/hr (As per experience)</strong...
Organize project post mortems and create a recommendations report to identify successful and unsuccessful project elements to pay attention to for future projects. What are we looking for in our Sr Project/Program Manager?. Lead and manage parallel projects through the full project lifecycle. Dev...
Proven experience as a Technical Project Manager with a focus on Infrastructure or Software Development projects. We are seeking an experienced Technical Project Manager with a strong background in Infrastructure or Software Development. Utilize project management tools and methodologies to track...
Global Regulatory Affairs Operation（Sr. This position belongs to Global regulatory affairs department, serving the global Market which encompasses China US, EU, AUS and others. This role requires a detail-oriented professional who can oversee all regulatory affairs and quality assurance activitie...
The Director of Policy and Regulatory Affairs will be responsible for managing Elevate’s relationships and policy positions at PJM, federal and state regulatory agencies, and state legislative bodies. Director of Policy and Regulatory Affairs – PJM Region. The position reports to the Vice Preside...
You understand that when it comes to customs and compliance, the details matter. Support import compliance issues, CF28, CF29, Quantity Adjustment filings and communications with Customs Brokers and CBP. Updates import-export compliance manuals - standard operating procedures regulations. In comp...
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...
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...
For the HR Compliance Specialist position, this role will require creating and maintaining policies and procedures. The position will plan, direct, or coordinate activities for the company to ensure compliance are within ethical and regulatory standards including ACA, HIPAA, and more. Collaborate...
Responsible for managing large, strategic ERP projects from initiation through delivery and leading internal and external project team members on implementation, migration, enhancement, or integration projects that often involve business process reengineering. Innovative and fast-growing company ...
Bank located in NJ is looking to hire a Fair Lending Compliance Analyst. Develop, implement, and oversee the Bank’s Compliance Fair Lending Monitoring Program to ensure compliance with all fair lending laws, regulations, and guidance. Conducts data analysis of the Bank’s consumer compliance data,...
The Director, Regulatory Affairs should have an advanced degree, preferably in the sciences, and have demonstrated application of regulatory expertise by at least 8+ years pharmaceutical industry experience. The Director, Regulatory Affairs is required to have excellent written and oral communica...
