The Regulatory Associate will report to the Senior Manager, Regulatory Affairs and, under the direction and guidance of the Associate Vice President, will help to ensure regulatory compliance of Prestige marketed products. Regulatory Affairs Associate (Tarrytown, NY). Assist with regu...
Safe Flight has an immediate opening for a Program Manager will ensure that assigned project-based programs adhere to established schedules, specifications, and budgets. Safe Flight’s benefits include employer-funded health care, on-site lunch program, 401K contribution, Wellness and Education...
The Senior Project Manager (SPM) is responsible for providing technical project planning, management and oversight for key initiatives and software implementation projects, ensuring first that these initiatives and projects are closely aligned with The Company's strategic priorities, and second,...
The Manager, Regulatory Affairs will report to the Global Regulatory Liaison (GRL) and provides support to the GRL in all aspects of regulatory affairs related to the development of novel therapeutics including quality, preclinical and clinical areas of drug development and the policies/procedures r...
The Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide regulatory leadership on the project teams in this area. Utilize regulatory expertise and knowledge of regula...
The Associate Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide regulatory leadership on the project teams in this area. Utilize regulatory expertise and knowledge...
This management position in Regulatory Affairs involves the ability to lead and manage a Therapeutic Area (TA) within Regenerons Regulatory Affairs organization so that all corporate objectives are met within specified timelines and so that the necessary state of compliance is maintained relative to...
Regulatory Affairs Certification (RAC) is a plus. Demonstrated expertise in preparing CMC sections of regulatory submissions (e. Strong understanding of global regulatory requirements, guidelines, and expectations related to CMC for pharmaceutical products (e. Experience with regulatory submissions ...
Senior Application Analyst with Security Operations / Compliance qualifications. The Senior Applications Analyst - Application Security Operations is responsible for managing and maintaining the security model of the Infor FSM (Finance & Supply Chain Management) ERP ecosystem. The Senior Application...
Perform the compliance activities of the portfolio to determine regulatory impact and associated submission requirement for clinical and commercial regulatory filings with country specific regulatory mentorship documents. The candidate will be leading the regulatory strategies for biologic products ...
Creates and maintains supporting project documentation; Communicates with project teams and stakeholders to ensure continuing alignment with project objectives. Creates and maintains supporting project documentation; Communicates with project teams and stakeholders to ensure continuing alignment wit...
As our Content and Project Manager Assistant on the Business Insurance team, you'll work closely with our national Risk, Industry, and Claim Practice leaders and will be responsible for supporting a variety of interesting projects. Learn more about what makes us different and how you can thrive as a...
In addition, Senior Regulatory Affairs Associate is responsible for supporting a variety of activities in the department related to regulatory submissions and R&D requests, and supporting other departments within the organization. Ability to review regulatory and scientific submission documents ...
The Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide regulatory leadership on the project teams in this area. Utilize regulatory expertise and knowledge of regula...
This management position in Regulatory Affairs involves the ability to lead and manage a Therapeutic Area (TA) within Regeneron’s Regulatory Affairs organization so that all corporate objectives are met within specified timelines and so that the necessary state of compliance is maintained relative t...
The Manager, Regulatory Affairs will report to the Global Regulatory Liaison (GRL) and provides support to the GRL in all aspects of regulatory affairs related to the development of novel therapeutics including quality, preclinical and clinical areas of drug development and the policies/procedures r...
The Associate Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide regulatory leadership on the project teams in this area. Utilize regulatory expertise and knowledge...
Project Manage multiple strategic projects concurrently. Experience managing the entire SDLC beginning to end for business applications and the required project artifacts (project plans, requirements, test plans, etc). Drive project working group meetings. Facilitate communications with the applicat...
Experience with major retailer compliance requirements, routing guides, and vendor violation processes. Previous compliance experience working with major Big box retailer. ...
Manage regulatory correspondence mainly to CDER, FDA, User fee staff, drug listing and Board of Pharmacies for state licensing submissions. Provide regulatory guidance to R&,D, Technical Operations Sales and Marketing, Quality, Clinical, Legal. Provide guidance and advise management regarding improv...
Perform the compliance activities of the portfolio to determine regulatory impact and associated submission requirement for clinical and commercial regulatory filings with country specific regulatory mentorship documents. The candidate will be leading the regulatory strategies for biologic products ...
Under direction, the selected candidates will work as Project Managers with the responsibility of managing projects related to water supply, wastewater, water quality protection, and other DEP initiatives. Other responsibilities would include project planning, environmental and economic analyses as ...
The Regulatory Associate will report to the Senior Manager, Regulatory Affairs and, under the direction and guidance of the Associate Vice President, will help to ensure regulatory compliance of Prestige marketed products. Assist with regulatory affairs projects and initiatives as needed, including ...
The incumbent will be a key contributor in identification of high food safety risk sites and create glidepath to continuous improvement processes for food safety programs and processes within such sites for North America foods and affiliated imported product suppliers. Working with PFNA Supply Chain...
Reviews the Compliance PATS work queue and assigns the new hire and employee actions to appropriate Compliance Specialists. The Bureau of Human Resources and Labor Relations Seeks a Principal Administrative Associate- Level I to serve as a Compliance Specialist. Communicates with hiring programs reg...