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....
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...
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...
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...
Eligibilities & qualifications....
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 ...
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...
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...
As a Project Manager specializing in utilities engineering, you will be responsible for leading and overseeing projects related to utility design, coordination, and construction. Elmwood Park, New Jersey is seeking a Utility Project Manager to join our team. Lead and mentor a multidisciplinary proje...
As a IT Program Manager, you will be responsible for overseeing and managing the successful delivery of complex IT projects/Programs within our organization. We are seeking a highly skilled and experienced IT Program Manager to join our dynamic team. ...
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...
Due to expansion, our multi-discipline firm is seeking a full-time Senior Project Manager. Our project portfolio includes private, municipal, county, and regional clients; some have been with our firm for three decades. Oversee the development of scopes of work, budgets, plans, as well as the execut...
I The Compliance Specialist may assist the Regional Compliance Officer(s) with other aspects/projects/tasks/reviews of the Compliance Program to assure compliance with licensure, accreditation and other applicable state and federal regulations. Provides input into the development of the annual Audit...
The Merger and Acquisition IT Project Manager will be responsible for assisting the project team in the integration/divestiture of the Seller’s/Buyer’s IT technologies to/from the client through the use of standard internal applications and tools. Skilled in establishing detailed scope, schedule, re...
The Program Manager (PM) will be responsible for planning and executing logistics for professional education speaker programs and activities. Database all program information and provide regular reports to the client on program status, program evaluations, financial status, and HCP-spend tracking. A...
We are looking for a Project Manager for a market leader in Clinical Trial Supplies!. Your responsibilities will include overseeing the entire lifecycle of Clinical Trial Services projects from the start and the planning plus management of each project. If you are a motivated Project Manager looking...
The appropriately qualified applicant will be able to demonstrate an established career as a Senior Program Manager working in commercial real estate sector programs on office corporate interiors project including vertical facilities construction, interior rehabilitation, multi-site construction log...
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...