QC Analyst Salary at Biomarin BETA

Job ID: 25-07654 Job Title: Analyst, QC Critical Reagents Duration: 12 months, 40 hrs / week Location: Novato, CA SUMMARY The QC Critical Reagents Analyst is responsible for maintaining the *** Critical Reagents program for commercial products in the global network, including but not limited to reagent preparation, maintaining material inventory, generating technical documentation, and supplying materials to the global testing network. Materials in the Critical Reagents program include qualified reagents, reference standards, custom reagents, analytical cell banks and other important materials that require dedicated oversight. The individual prepares trend graphs and analyses for Critical Reagents to support routine requalification activities, regulatory responses, and investigational activities. RESPONSIBILITIES Responsible for critical reagent acquisition, preparation, and aliquoting. Coordinates qualification testing with laboratory personnel Coordinates and executes critical reagen

Location: Novato, CA Zifo is hiring for a Business Systems Analyst (BSA) to work in the R & D area with one of our pharmaceutical clients. The BSA will implement instrument systems and software that meet the client's business needs. The BSA will help ensure systems are implemented efficiently, following a standard process to deliver systems that meet business needs, enhance compliance, improve efficiency, and reduce regulatory risk. **This role requires 100% on-site presence at the client site in Novato, CA** **This role is not eligible for relocation assistance** Responsibilities: Interface instruments, instrument workstations with systems/software Perform testing and ensure system meets business needs. Resolve defects Analyze, develop, document data flows/ process maps Collaborate with cross functional stakeholders to perform proof of concept (POC) testing. Develop, review, and obtain approval of SDLC documentation. Partner with the lab users and business SME's to ensure software mee

Politicom Law LLP is a women/minority-owned boutique political compliance law firm specializing in lobbying reporting requirements, campaign finance regulations, political action committee administration, and government ethics compliance across the United States. Our team is dedicated to providing innovative solutions and best-in-class client service in the ever-evolving field of political law compliance. Position Description: We are seeking a highly motivated and detail-oriented Project Manager to partner with our team of Political Reporting Analysts. The Project Manager will play a key programmatic role, ensuring the accurate, timely, and compliant delivery of client services. The ideal candidate will have experience in legal compliance, excellent project management skills, including attention to detail, and the interpersonal skills to foster a collaborative, high-performing team environment. Responsibilities: · Partner with a team of Political Reporting Analysts responsible for prep

Overview: Lewis Brisbois, an AmLaw 100 firm with 1,500+ attorneys and 55 locations servicing 40+ practice areas, is actively seeking a Practice Management Analyst with a minimum of 2 years of relative experience. The Practice Management Analyst will report to the Manager of Practice Management and National Managing Director, Practice Management. The Practice Management Analyst will provide administrative and operational support on standard Practice Management Department tasks as well as on other projects as assigned to meet Firm goals and objectives. Responsibilities: Job Responsibilities Data entry within Client & Rate databases, new client & assignment information and matter closures. Revise database records as identified during QC process. Assist Practice Management Specialist in sending Outlook email reminders to Attorneys consistent with Client requirements upon initial Client rate and case assignment. Assist Practice Management Specialists in sending follow up emails to Attorneys

Job Title: Analyst, QC Critical Reagents Duration: 12 months, 40 hrs / week Location: Novato, CA SUMMARY The QC Critical Reagents Analyst is responsible for maintaining the *** Critical Reagents program for commercial products in the global network, including but not limited to reagent preparation, maintaining material inventory, generating technical documentation, and supplying materials to the global testing network. Materials in the Critical Reagents program include qualified reagents, reference standards, custom reagents, analytical cell banks and other important materials that require dedicated oversight. The individual prepares trend graphs and analyses for Critical Reagents to support routine requalification activities, regulatory responses, and investigational activities. RESPONSIBILITIES Responsible for critical reagent acquisition, preparation, and aliquoting. Coordinates qualification testing with laboratory personnel Coordinates and executes critical reagent distributions f

SUMMARY The company is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases. We target diseases that lack effective therapies and affect relatively small numbers of patients, many of whom are children. These conditions are often inherited, difficult to diagnose, progressively debilitating and have few, if any, treatment options. The company will continue to focus on advancing therapies that are the first or best of their kind. The company's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinati

Company Description About Veolia North America A subsidiary of Veolia Group, Veolia North America (VNA) offers a full spectrum of water, waste and energy management services, including water, and wastewater treatment, commercial and hazardous waste collection and disposal, energy consulting and resource recovery. VNA helps commercial, industrial, healthcare, higher education, and municipality customers throughout North America. Headquartered in Boston, Mass., Veolia North America has approximately 10,000 employees working at more than 350 locations across the continent. Please visit our website www.veolianorthamerica.com. Job Description Pay Rate: $95000 to a maximum of $115000 Per Year. BENEFITS Veolia's comprehensive benefits package includes paid time off policies, as well as health, dental and vision insurance. In addition, employees are also entitled to participate in an employer sponsored 401(k) plan, to save for retirement. Pay and benefits for employees represented by a union a

Summary Join a leading company in delivering therapeutics for patients with serious and life-threatening rare genetic diseases. We focus on advancing therapies that are the first or best of their kind, targeting diseases that lack effective therapies and affect small numbers of patients, many of whom are children. Our Technical Operations group is responsible for creating drugs for clinical trials and scaling production for the commercial market. This team ensures regulatory standards are met and coordinates the worldwide distribution of our drugs to patients. Make a meaningful impact on patients' lives by joining our team. Responsibilities Responsible for critical reagent acquisition, preparation, and aliquoting. Coordinate qualification testing with laboratory personnel. Execute critical reagent distributions for the global testing network. Utilize LIMS to document acquisition and preparation of critical reagents, monitor testing status, and extract data for trend analyses. Generate