Provide consultation and advice to regulatory specialists regarding change control and product development. Offer regulatory direction and interpretation on team activities. Apply regulatory knowledge to support product-related activities. Prepare regulatory submissions and registration documents fo...
Catalent Pharma Solutions in Somerset, NJ is hiring a Senior Regulatory and Compliance Specialist for the Compliance Group. The Senior Regulatory and Compliance Specialist candidate must be knowledgeable in global regulations pertaining to the pharmaceutical industry and their impact on manufacturin...
The Senior Regulatory and Compliance Specialist candidate must be knowledgeable in global regulations pertaining to the pharmaceutical industry (or regulated industry equivalent) and their impact on manufacturing processes and practices. This role has high visibility within the Somerset site and the...
The Senior Regulatory and Compliance Specialist candidate must be knowledgeable in global regulations pertaining to the pharmaceutical industry (or regulated industry equivalent) and their impact on manufacturing processes and practices. This role has high visibility within the Somerset site and the...
The Senior Regulatory and Compliance Specialist candidate must be knowledgeable in global regulations pertaining to the pharmaceutical industry (or regulated industry equivalent) and their impact on manufacturing processes and practices. This role has high visibility within the Somerset site and the...
The Senior Regulatory and Compliance Specialist candidate must be knowledgeable in global regulations pertaining to the pharmaceutical industry (or regulated industry equivalent) and their impact on manufacturing processes and practices. This role has high visibility within the Somerset site and the...
We are seeking a highly skilled BCBA QA Specialist with experience in the. Review ABA treatment plans for clinical and insurance compliance. Ensure proper authorization approvals and compliance with audits. Proven experience as a QA specialist in the ABA field. ...
Cherry Hill Programs brings the magic to every experience by capturing moments that last a lifetime. In partnership with retail locations, tourist attractions, and destinations across North America, Cherry Hill Programs contributes millions of holiday and souvenir experiences for children and famili...
Responsible for all activities involving quality assurance and compliance with applicable regulatory requirements. Can serve as Quality Assurance representative on facility projects. Minimum of 2 years in a Quality Assurance role. This experience should be in the areas of the Quality System that inc...
Reporting directly to the Chief Scientific Officer, the Head of Regulatory Affairs will manage the regulatory team and work closely with R&D, Technical Operations, Clinical Development, and external consultants. Minimum of 10-15 years of experience in regulatory affairs within the pharmaceutical or ...
Working within the Climate Adaptation and Cities Team, the Cities Forestry Project Manager will lead and support the implementation urban forest plans, strategies, and projects in Newark and Paterson. In collaboration with the Cities team, the Cities Urban Forestry Manager will lead, develop, manage...
Manage project schedules and scope, assist in creating the project budget, oversee deliverables for quality and assist in staffing projects. Lead small project management teams assisting in project managing components of a larger technological program. Identify and mitigate risk through status repor...
Commercial bank located in Fort Lee, NJ looking to bring on board a “Fair Lending Compliance Technical Business Analyst” to join their team. Work closely with Fair Lending Compliance, IT, Product, Engineering, and Data Science to continuously enhance the API framework by identifying bugs, automation...
The Manager of Regulatory Affairs will lead the regulatory strategy and submission processes for Chemistry, Manufacturing, and Controls (CMC) associated with Abbreviated New Drug Applications (ANDAs) and generic products. Minimum 5 years of experience in regulatory affairs within the pharmaceutical ...
Define program resource needs and negotiate program resourcing plans. Understanding of milestone-based program planning (Daily Standup, risk register management, visual planning) for ongoing projects. Work with functional leaders to ensure the appropriate core team resources are committed to the pro...
Our client is seeking a Senior Staff Technical Program Manager (TPM) to lead the management and execution of server platform programs throughout the product lifecycle. Collaborate with Marketing and Architecture teams to translate product specifications into program deliverables. Conduct weekly prog...
Are you looking to advance your career and flex your Leadership and Program Finance skills in a fast-paced and rewarding organization? Join us! As Program Finance Manager II, you will be responsible for leading the Program Finance team in implementation and management of the integrated program manag...
Develop strategic direction and provide leadership for all regulatory interactions with FDA/global regulatory authorities . Those aren’t words that are usually associated with a job. Develop global and/or US regulatory strategy for Oncology products in development and through life cycle management, ...
Conducts project management training workshops and serves as a mentor to associate project managers and project managers. This positions report to the Technical Manager for the region but coordinates heavily with the Division Manager, Sector Manager, and Regional Business Development and Sales Direc...
The Project Manager will oversee the development of complex projects, ensuring adherence to cost, quality, safety, and timelines. Responsibilities include defining project specifications, planning implementation, and managing budgets while coordinating the efforts of various team members. Monitor pr...
TGRC is seeking a proactive and experienced Project Manager for a pioneering Green Hydrogen project based in New Jersey. Project Manager - Green Hydrogen. The position is contracted for 12 months, with a strong likelihood of extension depending on project performance and milestones achieved. Project...
Audio/Visual Program Manager - Mercer County, NJ. The ARC Mercer is seeking a skilled and experienced Audio/Visual Program Manager to join out dynamic team. As an Audio/Visual Program Manager, you will be responsible for overseeing the planning, execution and management of audio/visual projects acro...
CRM performs work on a variety of regulatory compliance related matters. The CRM team is an oversight control function within BX Central Legal & Compliance designed to assess the effectiveness of BX’ policies and procedures, particularly with respect to regulatory compliance of the BX registered...
The IT Compliance Analyst for our client is responsible for ensuring our compliance with Sarbanes-Oxley 404 (SOX) reporting requirements, and assisting in our other Information Technology initiatives, such as implementation of SOX framework, reviewing/validating SOC reports and assure that our syste...
The Compliance Specialist will also contribute to a range of compliance-related projects and provide administrative support. Compliance Specialist - Contract - Remote. Proclinical is seeking a dedicated Compliance Specialist for a contract role. Compliance Specialist's responsibilities will be:. ...