Regulatory Affairs Specialist: Average Salary in Franklin Lakes, NJ in 2024

DSI) is an industry leader in the science of hemostasis and thrombosis.Stago provides the total commitment of global resources and responsiveness, coupled with cutting edge technology and reliability.DSI is dedicated to continually developing and providing the very best h....

They engage in correspondence, meetings, and interactions with the FDA to address regulatory inquiries, respond to requests for additional information, and seek clarification on regulatory matters under the guidance of the Director, US Market Access. Analyzes and communicate the adequacy of proposed...

Assist the Manager of Regulatory Affairs during cGMP, Environmental, and Regulatory audits. Assist the Manager of Regulatory Affairs during periodic quality reviews, regulatory updates, and annual GMP training. Reports to: Manager of Regulatory Affairs. Responsible for facility registrations, renewa...

Regulatory Affairs Specialist (Medical Device). Zing Recruiting, in partnership with an established medical equipment manufacturer stationed in Parsippany, New Jersey is on the search for an experienced Regulatory Affairs Specialist to join their team. Regulatory Affairs Specialist Responsibilities....

Assist the Manager of Regulatory Affairs during cGMP, Environmental, and Regulatory audits. Assist the Manager of Regulatory Affairs during periodic quality reviews, regulatory updates, and annual GMP training. Responsible for any additional duties or assignments as directed by Manager of Regulatory...

Regulatory Affairs Specialist (Medical Device). Zing Recruiting, in partnership with an established medical equipment manufacturer stationed in Parsippany, New Jersey is on the search for an experienced Regulatory Affairs Specialist to join their team. Regulatory Affairs Specialist Responsibilities....

DSI) is an industry leader in the science of hemostasis and thrombosis.Before applying for this role, please read the following information about this opportunity found below.Stago provides the total commitment of global resources and responsiveness, coupled with cutting edge technology and reliabil...

They engage in correspondence, meetings, and interactions with the FDA to address regulatory inquiries, respond to requests for additional information, and seek clarification on regulatory matters under the guidance of the Director, US Market Access. Analyzes and communicate the adequacy of proposed...

They engage in correspondence, meetings, and interactions with the FDA to address regulatory inquiries, respond to requests for additional information, and seek clarification on regulatory matters under the guidance of the Director, US Market Access. Analyzes and communicate the adequacy of proposed...

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, a...

They engage in correspondence, meetings, and interactions with the FDA to address regulatory inquiries, respond to requests for additional information, and seek clarification on regulatory matters under the guidance of the Director, US Market Access. Analyzes and communicate the adequacy of proposed...

Assist the Manager of Regulatory Affairs during cGMP, Environmental, and Regulatory audits. Assist the Manager of Regulatory Affairs during periodic quality reviews, regulatory updates, and annual GMP training. Responsible for facility registrations, renewals, and document submissions to regulatory ...

Eligibilities & qualifications....

Responsible for ensuring product compliance standards and industry regulations are adhered to. Work with customers (mainly domestic) and factories/vendors in China to meet compliance and regulatory requirements. Experience with Walmart or Petco nonperishable product compliance. Seeking someone with ...

GGG is seeking a detail-oriented and self-motivated Food Regulatory Labeling professional to join our team in the Paramus, NJ office. ...

In-depth knowledge and experience of regulatory CMC documents review, and approval is required. Provide regulatory guidance to cross functional teams on product development, manufacturing, testing and commercialization of various complex drug products and dosage forms. Bachelor’s degree with 8...

Reporting to the Executive Director of Clinical Operations, this Program Manager will:  . Lead the multidisciplinary team members of Massive Bio to ensure trial success and replicate the success for all trials; the program leadership requires significant amount of data analysis, interpreta...

Hanwha Vision America (HVA) is seeking a Program Manager to help us unlock the full potential of our existing infrastructure, sales force and global programs to grow revenue with global end-user accounts. They will also identify opportunities to utilize our current pricing programs and maximize the ...

The Compliance Data Analyst I will report to the GRC Senior Compliance Associate, and assist with ongoing data remediation, data quality checks, license verification from respective state boards to ensure federal, state and EU disclosure reports are reported timely and accurately on behalf of OAPI a...

The Gateway Development Commission (GDC) is seeking a skilled Program Manager II (Sustainability) to coordinate the preparation and implementation of key sustainability planning documents for various contract packages within the Hudson Tunnel Project (HTP) and other Commission-managed projects. The ...

Dewberry is seeking an Environmental Compliance Specialist with 1-4 years’ experience to be located in our Parsippany, NJ office. These screenings will be conducted by Dewberry’s background vendor of choice and will be conducted in compliance with all applicable federal, state, and local law. ...

As a member of the NERC Compliance Group, you will perform governance and oversight of PSEG's compliance with the NERC Critical Infrastructure Protection (CIP) Reliability Standards. Bachelor's degree in Engineering, Compliance, Computer Science or a related field with a minimum of 4 years of equiva...

Langan is seeking a Senior Environmental Project Manager with a specialization in Data Centers and Critical Facilities to join its national practice. Lead environmental and multi-discipline efforts on a variety of project sites, with a focus on data centers, including performing complex analyses for...

Ensure and/or perform daily/weekly/monthly compliance inspections as required by Permit. Keep an active file of all facility operational permits and work with Facility Manager & Manager Permitting Compliance on permit updating and renewal as necessary. Audit Clean Earth of North Jersey units to ensu...

We are looking for a dynamic, hard-working individual to join our Global Compliance team as Compliance Analyst covering core compliance functions such as personal trading, gifts and entertainment, code of ethics reporting and regulatory filings. Serve as the day-to-day Compliance contact for employe...