The Policy Section in the Communications and Water Policy (CWP) Branch within the Public Advocates Office is seeking a Public Utilities Regulatory Analyst I-II to join its Policy team. Under the direction of the Program and Project Supervisor, the analyst will participate in several proceedings and ...
Create and execute complex regulatory implementation strategies for assigned legislative, regulatory, sub-regulatory, and licensing / accreditation requirements across multiple jurisdictions, including assessments of the regulatory impact of changes to people, processes, and technologies deployed ac...
The analyst will make recommendations based on independent analysis of regulatory, policy and technical issues. Under general direction of the Project and Program Supervisor, the analyst will support the Electric Market Design Section in the development of work products that are used to advise and a...
Individuals interested in applying for this vacancy must have eligibility.If you are new to state service or need to gain eligibility to these classifications, please click or to open the examination bulletin and follow the instructions on “How to apply”.The examination is a separate process from ap...
We have an opportunity to join the Alliance as a Provider Data Analyst II in the Operations Management Department. Performs data analysis and research to support provider data management strategies. Data transmission, provider file formats, such as 274, provider rosters, provider directories, HIPAA,...
The Business Analyst I will administer and oversee department project processes, submit purchase requisitions, and ensure that the procurement approvals are processed in accordance with department policies and procedures. ...
Collaborate across all phases (design, implementation, testing) of an engineering project and ability to partner multi-functionally - Build project plans and schedules, track and prioritize tasks across multiple product releases and efforts, simultaneously - Identify and resolve conflicts, inter-dep...
Builds relationships with internal team members (Project Managers, Project Engineers, Accounting team, Estimators) & develops an understanding of the roles/responsibilities of other departments within the project process. Our core values: Integrity – our word is our bond, and we do what we say, Resp...
Environmental Permitting and Compliance Specialist). Environmental Permitting and Compliance Specialist). Join Yorke Engineering, LLC, an Environmental Consulting leader in California that implements Environmental Engineering and Compliance solutions for our clients throughout California. Our missio...
The Regulatory Specialist is a part of Research and Development, this team is responsible for assessing ingredient safety and regulatory compliance, coordinating safety, micro, stability, compatibility and claims testing, ensuring product compliance with international cosmetic regulations, and advis...
Regional Compliance Specialist. Assist in turning around low-performing divisions' compliance numbers and contribute to the continuous improvement of the company’s compliance program and processes. In collaboration with Region Safety Directors, GMs, and division safety, develop and implement strateg...
The Ideal candidate will have 3 years of experience as a Business Analyst within D365 FO and is looking for someone to work Hybr. ...
Senior Regulatory Affairs Specialist. Draft, edit, and compile technical documentation and design dossiers to support CE mark/UKCA mark regulatory filings. Prepare regulatory submissions for FDA 510(k) clearance and A2F submissions. Research regulatory requirements from FDA, CMDR, MDR, IVDR, and UK ...
Primary Skills: Tableau, SQL, Debugging, Business Intelligence, Data Analysis Contract Type: W2 Duration: 6 Months (Possibility of Extension) Location: Santa Clara, CA (Hybrid) Pay Range: $60 - $65. Per Hour on W2 Grow your skills by working with industry leaders JOB RESPONSIBILITIES: Analyze comple...
Senior Clinical Data Analyst with healthcare data management, advanced analytics, m. EPIC Clarity and medical claims data) experience. Experience working with federal and state healthcare data repositories (e. ...
Senior/Principal Regulatory Specialist (Hybrid). Lead regulatory strategy and submissions (PMA, IDE) for Class III medical devices. Support global regulatory registrations and maintain compliance. ...
Advanced SQL skills to get the data you need from a data warehouse and perform data segmentation and aggregation from scratch. Data query and data processing tools/systems (e. Ability to grasp quickly and get up to speed on instrumentation, clickstream data, data architecture, and complex business s...
We are currently seeking a Senior Regulatory Affairs Specialist to drive regulatory strategies and submissions for medical devices. Senior Regulatory Affairs Specialist. Hands-on experience with major regulatory submissions and managing interactions with regulatory agencies. Develop and implement gl...
Our client is a growing company that has a product facilitating efficient data transfer by utilizing AI and Cloud Computing and is in need of a Program / Project Manager to assist with IT projects including an upcoming SOC 2 certification. Utilize JIRA Project Management, Service Desk, and Confluenc...
We are seeking a Principal Regulatory Affairs Specialist to support regulatory strategies and submissions for Class III medical devices. Lead regulatory submissions for Class III devices and maintain regulatory communications. This role will involve collaborating with cross-functional teams, contrib...
A degree in a life science, chemistry, or chemical engineering or closely related discipline with a graduate degree preferred and at least 10 years of experience in pharmaceutical regulatory affairs, that includes, but cannot be limited to, CMC regulatory affairs. Associate) Director, Regulatory Aff...
A medical device client of ours in the East Bay Area is looking to bring on a Regulatory Affairs Specialist IV position!. Years of Regulatory Affairs experience across the medical device space. International Regulatory Affairs Experience Required (Europe specifically). ...
Regulatory Affairs (strong preference for experience in oncology) in the biotechnology or pharmaceutical industries, including an in-depth knowledge and understanding of the regulatory environment. Develop and implement competitive and effective global regulatory strategies for oncology products inc...
Business Analyst & FP&A Functional Expert. This Business Analyst will report to the Director of Budget Services to provide essential support implementation and management of FP&A. We are seeking a highly motivated, driven, and intellectually curious Business Analyst to join our team. Financial Busin...
Chief Compliance Officer (San Francisco, CA): Our client, a successful hedge fund with approximately $3B in AUM, is seeking a talented and experienced CCO to help run all aspects of the compliance program. Manage the firm’s overall compliance program and develop, review, and update the firm's compli...