Director, Regulatory Affairs, Immunology. A company is looking for a Director / Sr. ...
The individual will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory support across all global projects; meet aggressive deadlines to ensure that regulatory agencies receive timely and quality submissions, shortening the review process and leadi...
You will lead the Regulatory Affairs department and report to the Vice President of Global Quality and Regulatory Affairs. The Director of Global Regulatory Affairs will be responsible for developing and executing regulatory strategies for drug development and commercialization ensuring compliance w...
This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on product labeling in collaboration with Global Regulatory Leads (GRLs). More Years of direct regulatory affairs experience, including US labeling expe...
A company is looking for a Regulatory Affairs and Compliance Director (Remote). ...
Director, Quality Assurance & Regulatory Affairs Atlanta, GA. Organizational responsibilities include site Quality Assurance, Quality Control and Regulatory Affairs documentation, and regulatory inspection / customer audit liaison activities. In this role, you will be responsible for the site Qualit...
The Director Regulatory & Scientific Affairs, Health & Wellness – North America is responsible for providing local technical support for the definition and execution of the commercial strategy in North America. This role works in conjunction with the Global RSA H&W Head, the Senior Director H&W RSA ...
The ongoing pace of regulatory uncertainty and economic volatility is unrivaled in the utility industry and requires equally unparalleled flexibility in ratemaking and regulatory strategies. GDS has been at the forefront of industry rate and regulatory policy, offering broad expertise in regulatory ...
The Program Manager works with many levels of leadership and staff to manage program efforts based on industry best practices; works as the single point of contact for facilitation and communication of program goals, deliverables, and schedules, and must be an excellent communicator; various levels ...
A company is looking for a Manager, Project Training to assist with client-specific initiatives in the biotechnology sector. ...
A company is looking for a Regulatory Affairs Manager, US Regulatory Lead, Rare Disease. ...
A company is looking for a Partner Now Assist Program Manager to support their Global Partnerships & Channels team. ...
A company is looking for an R&D Regulatory Specialist to develop and implement regulatory strategies for products in the biotechnology and pharmaceutical industry. ...
Manager, Regulatory Affairs III to provide strategic direction and operational support for CMC regulatory activities. ...
A company is looking for a Regulatory Affairs Specialist I to manage regulatory documentation and submissions. ...
A company is looking for a Project Manager to lead multiple programs across various business areas. ...
Manager, Regulatory Affairs III to provide strategic direction and operational support for CMC regulatory activities. ...
A company is looking for a Junior Program Manager to provide project control and contract administration for a large, diversified team. ...
Chemistry; advanced degree is a plus6+ years of pharmaceutical industry experience in CMC Regulatory Affairs, with a focus on small moleculesExperience in leading high-quality CMC regulatory submissions for global marketing applicationsStrong knowledge of global regulatory guidelines (FDA, EMA, ICH)...
A company is looking for a Regulatory Affairs Manager, US Regulatory Lead, Rare Disease. ...
A company is looking for a Senior Regulatory Compliance Specialist to assist with the implementation and maintenance of its Compliance Software Program. ...
A company is looking for a Program Manager - IT Collaboration to ensure seamless collaboration across various platforms in a remote or hybrid work environment. ...
A company is looking for a Regulatory Affairs Specialist to support US and OUS regulatory activities for Class II and III products. CFR 820, MDR)Experience in regulatory affairs, clinical affairs, Quality, or Engineering is required. ...
Senior Regulatory Affairs Specialist - (Medical Device) - Hybrid/Onsite position in Georgia. Engage with regulatory authorities and agencies to facilitate product approvals and resolve regulatory issues. If you would like to learn more about this Regulatory Affairs Specialist opportunity, apply dire...
TITLE: Executive Regional Director (multi family affordable housing). The Regional Director is responsible for supporting and executing the company’s objectives by ensuring financial, operating and compliance standards are met in the Region. Assume other responsibilities as assigned by the Dir...