Chief Inspector Salary at Zipline BETA

Senior Laboratory Counsel????Office of the General Counsel, Stanford, California, United States????Compliance Legal???????Jan 09, 2025 Post Date???????105588 Requisition # Immediate opening for a full-time attorney in the Office of the General Counsel at Stanford University, supporting SLAC National Accelerator Laboratory.The attorney would report directly to the General Counsel of Stanford University, with day-to-day supervision provided by the Chief Laboratory Counsel. SLAC is a vibrant multi-program laboratory whose mission is to explore how the universe works at the biggest, smallest, and fastest scales and invent powerful tools used by scientists around the globe. As a U.S. Department of Energy (DOE) national laboratory managed and operated by Stanford, SLAC research helps solve real-world problems and advances the interests of the nation. SLAC and Stanford faculty, scientists, and engineers regularly collaborate with world-leading universities, institutes, and companies to perfor

Join Yorke Engineering, LLC, an Environmental Consulting leader in California that implements Environmental Engineering and Compliance solutions for our clients throughout California. Our mission is to solve environmental compliance problems for industrial and governmental/infrastructure facilities. We are a growing and dynamic organization of highly respected professionals. Yorke Engineering, LLC has assisted over 1,400 client organizations with their Air Quality and Environmental Compliance, Engineering, and Permitting needs. Our philosophy is to efficiently help government and industrial customers with the complex array of environmental laws and regulations. From simple permits to complex agency negotiations, from small companies to the largest of California’s organizations, Yorke successfully solves our clients’ Air Quality and Environmental challenges. Our team has over 1,000 years of combined environmental experience and consists of engineers and scientists that specialize in Air

Head of Quality San Francisco, CA The Company: Our client is an innovative start-up company that is developing advanced, cloud-controlled robotic systems that enable the production of individualized drugs at scale. Their customers include some of the largest global organizations in the advanced pharmaceutical manufacturing space. Based in San Francisco, California, our client is backed by many top-tier tech and life science investors, including Casdin Capital, Lux Capital, Y Combinator, and more. Position Overview: As the Head of Quality, you will lead the development and implementation of a robust ISO 9001:20XX quality system to ensure compliance with industry standards in a cGMP-regulated pharmaceutical and biopharmaceutical environment. Reporting directly to the CEO, your primary focus will be aligning quality initiatives with customer and regulatory requirements. As the Head of Quality, your role will include the following: Quality Leadership: Build and lead a quality team to devel

Manager/Senior Manager Clinical Quality Assurance We are seeking a skilled Clinical Quality Professinal to support study team compliance with national and international regulatory standards and guidelines for cell therapy products. This role offers the opportunity to contribute to a growing biotech focused on innovative therapies for oncology and autoimmune diseases. Key Responsibilities: Act as a Clinical Quality lead by ensuring study teams adhere to GCP and regulatory requirements. Develop and execute audit plans and strategies for ongoing clinical trials. Perform initial and ongoing audits of clinical vendors. Coordinate, plan, and conduct internal system audits and external site/vendor audits in accordance with GCP guidelines. Report audit findings to management, provide recommendations, and verify corrective actions. Support the development and maintenance of clinical SOPs, work instructions, forms, and templates. Develop and deliver GCP and inspection readiness training for staf

This is an exciting opportunity to lead and manage digital quality and data integrity compliance within a cutting-edge biologics manufacturing facility. You will be responsible for overseeing 2 functional teams for Digital QA and Document Management QA up to 30 team members. This is a once-in-a-lifetime Global Expat leadership opportunity within the World’s Largest biologics CMO expanding to 720 KL total mammalian cell culture manufacturing capacity with commercial monoclonal antibody, mRNA vaccine and ADC manufacturing capabilities. Your roles and responsibility will include: Provide Oversight of the newly established Data Compliance group overseeing data integrity compliance efforts consistent with GMP and site Quality policies. Overseeing the DI framework and constituent policies, procedures, tools, and checklists governing DI and Computerized System Validation (CSV) that effectively establish data risk management stewardship and accountability throughout data and system life cycle

Job Title: Vice President, Regulatory Affairs and Quality – R&D Clinical Science Purpose Of This Role Working with the Chief Medical Officer, the Vice President, Regulatory Affairs will provide strategic and day-to day leadership for the Company’s Regulatory Affairs department. The Vice President will develop and execute a Regulatory strategy, including appropriate staffing. He/She will work closely with the company’s Clinical Operations, Compliance, Legal, Manufacturing and Medical teams, to meet overall Company objectives. The Vice President, Regulatory Affairs will take the lead in all Regulatory aspects of drug registration applications, on a global basis and anticipate and ensure effective post-approval Regulatory activities and results. As a member of the Leadership Team, he/she will also contribute to the Company’s overall strategic direction and key tactical management issues. He/She will effectively represent the Company’s interests in regulatory and commercial discussions. Ma

Salary: $161,500.68 - $198,299.88 Annually Location : Oakland, CA Job Type: Full Time Exempt from Civil Service Remote Employment: Flexible/Hybrid Job Number: 25-AL030-01 Department: Office of the City Attorney Opening Date: 01/27/2025 FLSA: Exempt Bargaining Unit: TM1 The Position CITY OF OAKLAND EMPLOYMENT OPPORTUNITY DEPUTY CITY ATTORNEY III LABOR & EMPLOYMENT Recruitment is being conducted by the Office of the City Attorney. Salary: $161,500.68 - $198,299.88 annually Benefits: Health, dental, vision, pension, hybrid work-from-home, and other competitive benefits. Recruitment Opens: January 17, 2025 Deadline to Apply: Open until filled The Oakland City Attorney's Office seeks a well-qualified individual to join our office's labor & employment advisory unit. The incumbent will be exposed to a wide range of personnel matters across a variety of City departments, with an emphasis on police personnel matters including accountability and public-safety reform. Duties will include, but wil

Salary : $104,124.00 - $126,528.00 Annually Location : Emeryville, CA Job Type: Full-Time Job Number: 1800134 Department: Community Development Opening Date: 11/22/2024 Closing Date: Continuous Bargaining Unit: SEIU Description Under general supervision of the Chief Building/Fire Code Official or designee, performs complex and detailed inspections of structures for conformance to codes, ordinances, approved plans, calculations and specifications; reads and interprets construction drawings and specifications for compliance with codes, ordinances, energy and disabled access requirements; conducts investigations of suspected violations of the Municipal and Building codes, including code enforcement; may assist in training other Building Inspectors and providing direction to other technical and/or clerical staff, including temporary; employees. Performs related duties as required. CLASS CHARACTERISTICS This is a journey-level classification, which is defined as having practical experience