11 practicing attorney jobs found in california

job summary: Perform experiments, organize data and analyze results under minimal supervision. With minimal supervision, plans, conducts or monitors experiments, records and organizes data, analyses results, generates robust and reliable data and/or Ensures that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations. 90% lab work including sample isolation, drying, and testing location: New

job summary: A global Pharmaceutical company that harnesses the best of biology and technology to fight the world's toughest diseases, and make people's lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Our investment in research and development has yielded a robust pipeline that builds on our existing portfolio of medicines to treat cancer, heart disease, osteoporosis, inflam

job summary: The Staff Quality Engineer, Software will be the subject matter expert on providing guidance to the organization and the software teams in establishing policies and procedures for Software Design Control. This individual will be an integral part of the software development life cycle process in informing, guiding, and evaluating the teams' adherence to practices that would ensure compliance to required regulatory requirements. SKILLS REQUIRED

job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve thei

job summary: PRIMARY OBJECTIVE OF POSITION: Under minimal supervision, the Quality Specialist, Stability supports the stability program under regulatory requirements and ISO 13485 and runs stability studies from initial batch/lot selection to final report generation and study destruction; works closely with Quality, R&D, and Operations to assure appropriate batch/lot selection, initiation, and execution of Stability studies in a compliant and timely man

job summary: This is a high level contract role, requiring Direct Global Regulatory Labeling Operations Project Management experience in the Pharma/Biotech industry, as deep knowledge of pharmaceutical labeling regulations, compliance, and processes are critical for this role. The Labeling Project Manager is responsible for all activities associated with the development, creation and execution of labeling for assigned product lines for domestic and/or i

job summary: As a trusted staffing and recruitment partner, we are committed to connecting you with the perfect opportunity at a global leader in biotechnology. Leveraging our extensive network, we provide access to top-tier roles that allow you to grow and make a meaningful impact in the healthcare and life sciences industries. This company is dedicated to discovering and developing innovative therapies that address serious diseases, with a focus on onco

job summary: Under moderate supervision, the Stability Analyst will be part of the Quality team and responsible for performing stability testing of IVD and ASR products according to SOPs and in compliance with local and global QMS and regulatory requirements. Support the day-to-day activities of the Quality department while adhering to applicable regulatory requirements, ISO 13485, local and global QMS. location: Rocklin, California job type: Contract

job summary: We are seeking a Regulatory Submission Manager to support global regulatory initiatives and ensure compliance with regulatory requirements for investigational and marketed products. Role involves working closely with cross-functional teams and regulatory leads to support submission activities, labeling development, and strategic regulatory guidance. The ideal candidate has a strong background in regulatory submissions and document review, as

job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Internationally known for creating cutting-edge biopharmaceuticals for patients who live with rare

job summary: We are seeking a highly skilled Senior Manager - CMC Regulatory to lead the planning, preparation, and submission of global regulatory CMC-related content for clinical trial applications, marketing applications, and periodic reports. This role involves ensuring compliance with US and international regulatory requirements, collaborating with cross-functional teams, and providing strategic guidance on manufacturing changes to optimize regulator