Regulatory specialist jobs in Lodi, New Jersey (NJ) State

Product Stewardship Specialist. As a Product Steward - Safety and Health Information Specialist, you will play a crucial role in ensuring the safety and health information provided to Sika's Customers is accurate and compliant. ...

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...

You will support all regulatory-related activities, including but not limited to: researching industry updates pertaining to labeling compliance; supporting the review processes for packaging, marketing materials, and digital information. Research and consult on food labels, packaging, and other ...

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, ...

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...

The Staff Regulatory Affairs Specialist will work in BD Medical - Pharmaceutical Systems Business Unit taking on a lead role at the project level in developing and executing regulatory strategy and compliance plans to promote and support drug delivery solutions for pharma combination product deve...

The Regulatory Affairs Specialist (F&B) will be responsible to independently provide Symrise Inc. The Regulatory Affairs Specialist may provide support to the retrieval of revenue paid for the use of tax paid Distilled spirits in finished product materials and support other TTB related activities...

Responsibilities include managing the entire contract development lifecycle, as well as ensuring corporate regulatory and license compliance requirements are met. ...

Title: Regulatory Affairs Specialist (Must Have Medical Device Regulations). Job Category: Regulatory Affairs / Compliance. This position is responsible for leading regulatory submissions required to market medical devices in the U. Europe (and other international markets if needed such as China/...

The Staff Regulatory Affairs Specialist will work in BD Medical - Pharmaceutical Systems Business Unit taking on a lead role at the project level in developing and executing regulatory strategy and compliance plans to promote and support drug delivery solutions for pharma combination product deve...

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 ...

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

You will support all regulatory-related activities, including but not limited to: researching industry updates pertaining to labeling compliance; supporting the review processes for packaging ...

Quality Assurance Specialist - Pre-Litigation, NJ Overview: We are Brandon J. Broderick Attorney at ... Ensure all necessary legal and regulatory requirements are met staying up to date with industry ...

Job Description Compliance Specialist Summary Description Reporting to the Assistant Director of ... Act as assistant researcher regarding compliance and regulatory program standards and requirements ...

Contract and Compliance Specialist Department: Finance Reports to: Director of Budget and Grants ... regulations, and industry standards that may impact contract management practices, ensuring ...

Familiar with FDA, ISO, and other regulatory agency guidelines. * Understanding of Good Manufacturing Practices (GMP), Good Documentation Practices (GDP) and Good Laboratory Practices (GLP) required

BronxWork is Hiring (3) CQI Specialist for the Administration Department RESPONSIBILITIES * Lead ... law and regulations (e.g., HIPAA), contract requirements, agency and program policies and ...

Ensures regulatory compliance, timeliness requirements and accuracy standards are met. Coordinates efficient functioning of day-to-day operations according to defined processes and procedures

Bank Data Management Specialist - Contract - Weehawken, NJ - $40.00 - $49.00/hr. The final salary ... regulations such as BCBS 239, OCC Heightened Banking Standards, IFRS, and CCAR is preferred

Responsibilities include managing the entire contract development lifecycle, as well as ensuring corporate regulatory and license compliance requirements are met. The role also involves reviewing ...

Pharmaceutical Communications Specialist needed for a contract opportunity with Yoh's client in ... Manage administrative tasks for full Communications department, including Medical/Legal/Regulatory ...

... Specialist. Work schedule: 3 days a week onsite. Missions ... Perform all aspects of regulatory reporting level 2 control reviews:(identification of financial ...

Acts as liaison between principal investigators, sub-investigators, clinical research nurses and regulatory specialists on all regulatory issues and changes within the protocol. * In collaboration ...