The individual will be partnering with Regulatory Reporting Analysis team members and business stakeholders to assist with the automation efforts across all regulatory reports. Partner with Regulatory Reporting Analysis team members to understand current reporting procedures and manual processes per...
Autonomously support new product development core teams including development of regulatory strategies and the preparation of regulatory content for domestic and international submissions for IVD medical devices to support the core team's approved scope of regulatory activities, with focus on instru...
The individual will be partnering with Regulatory Reporting Analysis team members and business stakeholders to assist with the automation efforts across all regulatory reports. Partner with Regulatory Reporting Analysis team members to understand current reporting procedures and manual processes per...
Compile, prepare, and review regulatory submission to US and EU. Anticipate regulatory obstacles and emerging issues throughout the product submission. Provide regulatory input for responsible countries/region for product lifecycle planning. Monitor applications under regulatory review and communica...
Internal Job Title: Regulatory Affairs Associate II. Canada Chemical regulatory oversight and review. Position requires a Bachelor's degree in a science or chemistry-related field, coursework or certification in Cosmetic or Drug Regulatory Affairs. ...
Product Stewardship Specialist. Product Regulatory expert for Construction Chemical Company responsible for preparing and releasing product safety information for finished and intermediates products across all technologies. Product Stewards work closely with Local and Global Corporate Raw Material, ...
The individual will be partnering with Regulatory Reporting Analysis team members and business stakeholders to assist with the automation efforts across all regulatory reports. Partner with Regulatory Reporting Analysis team members to understand current reporting procedures and manual processes per...
Supports Regulatory Associate Director and team with the regulatory impact assessment, overall planning, validation of change scope and regulatory intelligence. Specialist/Coordinator, Regulatory Affairs. Partners very closely with Country Regulatory Affairs and the Outsourcing Partner (for some pro...
Autonomously support new product development core teams including development of regulatory strategies and the preparation of regulatory content for domestic and international submissions for IVD medical devices to support the core team's approved scope of regulatory activities, with focus on instru...
GGG is seeking a detail-oriented and self-motivated Food Regulatory Labeling professional to join our team in the Paramus, NJ office. ...
Senior Regulatory Affairs Specialist. Hiring - Senior Regulatory Affairs Specialist. Assess applicable change requests for regulatory impact and follow-up on related regulatory action items. Support marketing, R&D and Lonza BU in ad hoc projects, in relation to market growth and innovation initi...
The Senior Specialist is responsible for developing CMC regulatory submission strategies and timelines for assigned pharmaceutical projects/products in accordance with global regulations and guidance. The Senior Specialist is also responsible for the preparation and review of information required fo...
Assist the Manager of Regulatory Affairs during cGMP, Environmental, and Regulatory audits. Responsible for facility registrations, renewals, and document submissions to regulatory agencies (eg Drug and Cosmetic listings, etc), under the direct supervision of the Head of Quality/Regulatory. Assist t...
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....
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...
Provides guidance/direction within the regulatory department and stakeholder groups relative to regulatory compliance of client's products and processes. Independently support data maintenance and archival and retrieval of regulatory documentation in computerized systems. Assist with preparing h...
I look forward to hearing from you soonJob# 36317Job Title: Global Regulatory Affairs Documentation SpecialistLocation: Rahway, NJDuration: 12 months contract (Potential to extend)Benefits: Paid Sick Leave, Matching 401K and Health Insurance with minimum chargesFreyr is hiring for its direct client,...
Provides guidance/direction within the regulatory department and stakeholder groups relative to regulatory compliance of client's products and processes. Independently support data maintenance and archival and retrieval of regulatory documentation in computerized systems. Assist with preparing high ...
Lead the activities for preparing an oral solid dose manufacturing site for inspections by US FDA and applicable foreign regulatory authorities. Assist the site in preparing written responses to address the observations for customer audits, internal audits, corporate audits, and regulatory inspectio...
The individual will be partnering with Regulatory Reporting Analysis team members and business stakeholders to assist with the automation efforts across all regulatory reports. Partner with Regulatory Reporting Analysis team members to understand current reporting procedures and manual processes per...
Summary/Objective: GGG is seeking a detail-oriented and self-motivated Food Regulatory Labeling professional to join our team in the Paramus, NJ office. ...
We are seeking a dynamic and experienced Innovation Regulatory Specialist interested in further developing and drivingour growth of. Collaborate with cross-functional teams and our plant in Canada to resolve any regulatory compliance issues and provide solutions to meet regulatory requirements. The ...
Autonomously support new product development core teams including development of regulatory strategies and the preparation of regulatory content for domestic and international submissions for IVD medical devices to support the core team's approved scope of regulatory activities, with focus on instru...
Regulatory expert support IVDR teams, implements regulatory strategies for IVDR activities; provides regulatory leadership; collaborates with the regulatory staff from other business units, companies, government agencies as needed to develop harmonized policies, procedures and work instructions for ...
Compile, prepare, and review regulatory submission to US and EU. Anticipate regulatory obstacles and emerging issues throughout the product submission. Provide regulatory input for responsible countries/region for product lifecycle planning. Monitor applications under regulatory review and communica...