File Manager Salary at Cdc BETA

LANDSCAPE ARCHITECT OJB Landscape Architecture is a leading landscape architectural design firm with offices in Houston, Dallas, San Diego, Boston, and Philadelphia. A recipient of numerous design awards, our work includes the design of urban parks, academic institutions, healthcare campuses, workplace environments, and landscape master plans for private and public clients. OJB is currently accepting applications from mid-level Landscape Architects for our studios in Houston, Solana Beach, Boston, Denver and Dallas. Experience should include demonstrated success in project design, development, and construction. Responsibilities may include: Preparation, coordination and completion of design and construction document packages Development of creative technical solutions Coordination of design and engineering sub-consultants Development of project specifications Leading project meetings and demonstrating competent understanding of assigned projects Preparation of client presentations, pla

We're looking for an organized, tech-savvy, and reliable assistant to support a busy executive with administrative and personal tasks. This part-time role offers a mix of home office, business office, and occasional errand duties"perfect for someone looking for flexibility and variety. The schedule is flexible (8 to 10 hours per week).Key Responsibilities:Organizing files, managing mail, and scheduling tasksCoordinating travel and handling invoices/receiptsCalendar management and professional communicationRunning errands (personal and professional)Requirements:Reliable transportation and a valid driver's licenseStrong organizational skillsTech proficiency (Microsoft Office, Google Workspace, etc.)Business casual dress requiredFlexible hours, competitive pay, and a dynamic work environment.

For over 12 years FSLG has been committed to providing superior legal expertise in fertility and assisted reproduction. Our firm is looking for an experienced, highly proficient Legal Assistant with excellent attention to detail to join our team. This individual will assist with case management, legal research, client updates, information gathering, along with various administrative duties. · New case and client intake · Conduct legal research to support case preparation and strategy · Collaborate with team members to prepare for court hearings and filings · Provide clerical support including scheduling appointments, filing documents, and maintaining calendars. · Case/file management (data entry, tracking and recording) · Researching codes and regulations for state / insurance / random topics on the internet · Picking up and dropping of packages to court directly and/or agency · Run background checks · Various Administrative tasks including but not limited to: Answering phones Copying/

At SeaWorld, we're passionate about caring for animals. In fact, we've already rescued over 40,000 animals (and counting!). And we can save you from being stuck in just another job. Join us and help bring joy, excitement, and lasting memories to people from around the world. We're seeking enthusiastic, dedicated, and hard-working individuals to become our Ambassadors. Join us and play an important part on our incredible team! What you get to do: Provide a wide variety of support to the Human Resources department. As an HR File Clerk, you will play a crucial role in maintaining accurate and organized employee records and documents. You will ensure that all HR-related paperwork is filed and stored appropriately, making it easily accessible for HR staff and compliant with legal requirements. Organize, file, and maintain both physical and digital employee records. Ensure personnel files, benefits documents, and HR paperwork are systematically filed. Accurately enter and update employee inf

Background Experience: Bachelor’s degree in a life science, engineering, or equivalent required. Advanced degree preferred. Minimum of 6 years of experience in Regulatory Affairs, of which a minimum of 4 years must be in IVD Regulatory Affairs. Regulatory Affairs Certification preferred. Experience in regulatory submissions including 510(k) and IVDR technical documentation required. Experience in international registrations preferred. Project management experience preferred. Advanced knowledge of in vitro diagnostics regulations, guidances, and standards for obtaining domestic and international marketing authorizations and post-market vigilance. Advanced knowledge of regulatory intelligence tools and methods, with ability to interpret and apply regulations. Knowledge of electronic publishing/file management system. Advanced verbal and written communication skills including proofreading, scientific writing, presenting positive persuasive arguments, and presentation to various organizati

The Regulatory Affairs Manager will manage a team of three (3) technical staff to develop regulatory plans for products, to prepare regulatory submissions such as 510(k)’s and EU IVDR Technical Documentation to manage communications with Regulatory Agencies e.g. FDA, EU Notified Bodies and Health Canada. Background Requirements: Bachelor’s degree in bioengineering/biomedical engineering, biochemistry, chemistry, molecular biology, or related technical science discipline required. Advanced degree preferred. Regulatory Affairs Certification preferred 8+ years of experience in Regulatory Affairs 5+ years in IVD Regulatory Affairs. Minimum 5 years of experience in managing regulatory professionals directly Demonstrated success in obtaining regulatory approvals in the major geographies including but not limited to the US, EU (under IVDR) and other major geographies. Hands-on experience in preparing regulatory submissions including 510(k) and IVDR Technical Documentation and managing relatio

ASSISTANT DIRECTOR-ANALYTICAL DEVELOPMENT & QUALITY CONTROL Seeking an experienced analytical chemist to join our QC & Analytical Development group at the Assistant Director level. The ideal candidate will be a self-starter, familiar with a broad range of analytical techniques, possess a strong work ethic, have good communication skills, and have experience working in a GMP environment. The successful candidate will be able to perform the following responsibilities with a high degree of independence and attention to detail. RESPONSIBILITIES: Coordinate and execute testing of drug substance intermediate, drug substance, and drug product samples Develop drug substance specifications ensuring efficient integration across Chemistry, Manufacturing, and Controls (CMC) and other relevant disciplines such as Clinical and Toxicology Author scientific reports and portions of the CMC section of regulatory filings Manage the analytical activities for therapeutic development projects May develop an

A highly respected and well established LA based plaintiff firm is presenting a unique opportunity to a dynamic, highly motivated, results oriented Litigation/Trial Attorney. This position is ideal for a Litigation Attorney with 7 years of personal injury experience. Duties include but are not limited to: * Drafting pleadings and correspondence * Taking and defending depositions * Working with clients on day-to-day advice and opposing counsel inquiries * Law and Motion practice on cases * Drafting discovery (mostly meet and confer/motions side) * Document review * Attending court hearings as 2nd chair * Negotiate settlements for Legal Disputes * Comply with all legal standards and regulations * Perform administrative and management functions related to the practice of law Qualifications: * 7+ years Personal Injury Experience * Knowledgeable in Trial & Litigation Procedurals * Applicants must be licensed by the California State Bar * Excellent written and verbal communication skills * D