Manufacturing Controls Jobs in San Diego, CA

Roles & Responsibilities: 5 to 6 years of medical devices or diagnostic equipment manufacturing experience. Manage the end-to-end validation documentation lifecycle including authoring reviewing and approving protocols (URS IQ OQ PQ PV TMV RTM VSR) Change Controls and Periodic Review More...

Opportunity at a GlanceThe Senior Sales Contracts Analyst plays a critical role in driving operational excellence and legal compliance within the Workforce Solutions Sales Operations function. This role ensures sales contracts are reviewed executed and maintained with a high level of More...

The Vice President Regulatory Affairs & Quality Assurance is responsible for developing and executing global regulatory strategies aimed at the most efficient regulatory pathway and ensuring quality compliance for ORICs development programs. This position involves shaping and lead More...

What you will doUnder management direction is responsible for organization and implementation of plans procedures and policies necessary to maximize utilization of resources in line with area and plant goals. Incorporate core values of safety quality and employee relations. Manages al More...

Who We Are:At Neurocrine Biosciences we pride ourselves on having a strong inclusive and positive culture based on our shared purpose and values. We know what it takes to be great and we are as passionate about our people as we are about our purpose - to relieve suffering for people w More...

The Vice President Regulatory Affairs & Quality Assurance is responsible for developing and executing global regulatory strategies aimed at the most efficient regulatory pathway and ensuring quality compliance for ORICs development programs. This position involves shaping and lead More...

Coordinates study startup activities with the local project team and supports all processes critical for site activation.In the absence of stand-alone feasibility function leads activities in feasibility research and site identification process.Facilitates site agreement and/or budget More...

Strategic partner in supporting the growth and client development of our Financial Lines Claims consulting services including D&O E&O R&W Financial Institutions Fidelity/Crime Cyber and EPLI coverage lines.This position is part-time and flexible with a focus on business de More...

OverviewJob SummaryWerfen Autoimmunity Manufacturing Associates play a critical role in the manufacturing and/or testing of a variety of Autoimmune-related diagnostics products. This position is responsible for the manufacture and/or testing of components of diagnostic kits used by cl More...

The OpportunityQuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing clinical chemistry and transfusion medicine. We are more than 60 More...

What if the work you did every day could impact the lives of people you know Or all of humanityAt Illumina we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming More...

What The Role IsThe Manager Regulatory Compliance will assist in the management of the Clearway Energy Group electric regulatory compliance program and in administering facilitating and managing compliance with NERC and other federal electric regulatory requirements as well as state a More...

The Associate Director works independently with guidance from a Director and is responsible for developing and implementing the HEOR strategy and tactics supporting more than one indication within the same product or more than one product within the same indication either US or Intern More...

Summary:The Associate Director is responsible for leading all analytical activities for one or more projects. This position manages GMP analytical studies as well as authoring/reviewing of CMC sections for regulatory submissions. The position will work closely with the CMC lead as wel More...

Responsibilities: Develop and implement regulatory filing timelines for new and existing products in key markets such as US EU and Asia markets. Prepare and submit new global market device applications and amendments. Prepare and oversee the review of Traditional 510(k) Premarket Not More...

Please note that this position is can be based in San Diego CA South San Francisco CA or Princeton NJ. Acadias hybrid model requires this role to work in our office three days per week on average.Position SummaryThe Director of Regulatory Affairs (RA) Labeling will lead the developmen More...

Please note that this position is based in Princeton NJ or San Diego CA. Acadias hybrid model requires this role to work in our office three days per week on average.Position Summary:The Associate Director (AD) Clinical Trial Materials (CTM) plays a pivotal role in the success of clin More...

Position SummaryThe Senior Director Translational Biology will lead the strategy and execution of disease and drug mechanism of action (MoA) studies to accelerate the development of novel therapeutics from discovery through late-stage clinical programs. This role is critical to bridgi More...

Please note that this position can be based in San Diego CA OR Princeton NJ. Acadias hybrid model requires this role to work in our office three days per week on average.Position SummaryThe Regulatory Affairs Operations Manager is responsible for publishing QC and transmittal of eCTD More...

P-358This role can be remote andrequires candidates to be located in San Diego CA. Candidates from other areas will not be considered.At Databricks we are on a mission to empower our customers to solve the worlds toughest data problems by utilizing the the Databricks Data Intelligence More...