The AD CMC Regulatory Affairs supports the development and successful performance of the CMC regulatory strategy for the innovative pipeline of early-stage T cell therapies. This position is hybrid, and based in Santa Monica, CA and reports to the Executive Director, CMC Regulatory Affairs. You will...
Senior Associates, Associates, and Sr. Norton Rose Fulbright is seeking an associate with 4-8+ years of legal experience with respect to FERC electricity, with some exposure to project finance or project documents for energy transactions. The work will involve regulatory aspects of the development, ...
The AD CMC Regulatory Affairs supports the development and successful performance of the CMC regulatory strategy for the innovative pipeline of early-stage T cell therapies. This position is hybrid, and based in Santa Monica, CA and reports to the Executive Director, CMC Regulatory Affairs. Partner ...
Consumer Products Litigation & Regulatory Associate. The associate hired for this position will focus primarily on regulatory matters, including those involving the CPSC, FTC, and NAD. Affirmative regulatory reporting and responding to regulatory investigations. Dentons’ Consumer Products team h...
We are looking for a regulatory attorney with 2-4+ years of experience to join DISH Wireless L. Preparing and submitting regulatory licensing applications and responding to document requests from government agencies. An understanding of legal language, principles, research methods, and relevant gove...
A law firm in Los Angeles is seeking a highly motivated Regulatory Associate Attorney to join their team. The successful candidate will support the firm’s sophisticated regulatory and reimbursement practices and will be involved in a variety of challenging and evolving legal matters. Support the fir...
Corporate/Regulatory Associate. Our corporate/commercial health practice offers general counsel, health regulatory and governance advice to healthcare organizations, associations and professionals. We provide strategic advice and regulatory opinions on a wide variety of issues. ...
Associate) Director, Regulatory Affairs – Permanent – San Francisco Bay Area. Proclinical is seeking an (Associate) Director, Regulatory Affairs for a clinical-stage biopharmaceutical company located in the San Francisco Bay Area. A degree in a life science, chemistry, or chemical engineering or clo...
Manage Energy practice teams in regulatory-focused client engagements, including general and limited-issue rate cases, development of regulatory strategy, and regulatory due diligence for transactions;. Serve as a subject matter expert for clients on ratemaking issues and regulatory strategy;. Perfo...
The AD CMC Regulatory Affairs supports the development and successful performance of the CMC regulatory strategy for the innovative pipeline of early-stage T cell therapies. This position is hybrid, and based in Santa Monica, CA and reports to the Executive Director, CMC Regulatory Affairs. You will...
The Regulatory Associate will primarily focus on provider reimbursement issues, Medicare and Medicaid appeals, and audits and internal investigations, supporting the firm's robust and sophisticated regulatory and reimbursement practices. A leading national healthcare law firm is seeking a Remote Reg...
We are supporting a small growing biotech in the Bay Area looking for a Senior Regulatory Affairs Associate!. Atleast 2 years experience in a regulatory setting at a biotech company. Strong foundation in biological or physical sciences, with the ability to apply scientific knowledge to regulatory ma...
Our client is in search of candidates who demonstrate a keen interest and enthusiasm for tackling the intricate regulatory and policy challenges within the Medicaid program. This includes assisting with transaction structuring and negotiation, providing strategic counsel on regulatory and compliance...
Job Summary: Talent Software Services is in search of a Program Compliance Specialist for a contract position in Los Angeles, CA. ...
The Manager CMC Regulatory Affairs is responsible for supporting the development and successful performance of the CMC regulatory strategy for the innovative pipeline of early and late-stage T cell therapies. Director, CMC Regulatory Affairs. Represent CMC regulatory affairs on product teams and in ...
The Manager CMC Regulatory Affairs is responsible for CMC technical document review and writing, authoring and compiling the CMC sections for global regulatory filings by working closely with the cross-functional teams including CMC, Quality, Clinical and Regulatory Affairs to ensure all Regulatory ...
Program Compliance Specialist needs 5 years working experiences related to Workforce contract compliance requirements, data collection, document generation experience. Program Compliance Specialist requires:. Program Compliance Specialist duties:. Maintain the compliance database by tracking due dat...
Title: Regulatory Affairs Specialist with a Specialty in Labeling. Regulatory Affairs Certification is preferred but not required. Partners with other functions and Subject Matter Experts (SME's) to obtain information and/or data required for regulatory submissions. Anticipates regulatory obstacles ...
The Manager CMC Regulatory Affairs is responsible for supporting the development and successful performance of the CMC regulatory strategy for the innovative pipeline of early and late-stage T cell therapies. Director, CMC Regulatory Affairs. Represent CMC regulatory affairs on product teams and in ...
Regulatory Affairs Operations Specialist I. This new team member will perform specialized level work assignments and/or analyses, evaluation, preparation, and submission of documentation for the worldwide regulatory registration, ensuring products and procedures comply with regulatory agency specifi...
Maintain or create technical/regulatory documentation such as IL, QIL, QF and SDS. Review artwork for fill weight claims, ingredients and regulatory issues. Assist with developing technical documents for new/existing products to meet regulatory and customer needs. High school Diploma or GED and 1-3 ...
Provide administrative review and support (analyzing, processing and reporting) in the Customs compliance areas of internal compliance assessments, import or export compliance procedure manuals, classification, valuation, NAFTA, C-TPAT and various Customs programs in accordance with company policy, ...
Seeking a Regulatory Affairs Manager to support the Kindeva business in maintaining regulatory compliance of existing manufactured products for customers on a global basis by:. Managing regulatory compliance activities for Kindeva and existing customer products and registrations as required and prov...
Regulatory Affairs Advertising and Promotion (Ad/Promo) and Labeling is a core function within Kite’s Global Regulatory Affairs organization and acts as a critical strategic partner across cross-functional teams. Manager, Regulatory Affairs – Ad/Promo and LabelingJob Description. Regulatory Affairs ...
Seeking a Principal Regulatory Affairs Specialist to support the Kindeva business in maintaining regulatory compliance of existing manufactured products for customers on a global basis by:. Managing regulatory compliance activities for Kindeva and existing customer products and registrations as requ...