Top Biotech Jobs in San Diego, CA
The Feasibility Manager in the Precision for Medicine team oversees the management and delivery of various feasibility projects related to clinical trials. They conduct pre-award and post-award analyses, support business development efforts, and ensure the quality and accuracy of feasibility data and processes throughout the project lifecycle. The role involves collaboration with operational strategy teams and client interactions to support successful trial execution.
The Systems Engineer will lead the design and development of medical devices, focusing on user requirements, risk management, and compliance with FDA regulations. Responsibilities include managing the device user manual, collaboration with cross-functional teams, maintaining traceability, and ensuring the implementation of design controls.
The Intellectual Property Administrator will manage patent and trademark prosecution processes, coordinate with internal and external legal counsel, ensure compliance with filing deadlines, administer document processes for IP files, and enhance workflows within the company.
The Director, QTC Account Lead will manage business within their territory, drive the utilization of gene therapies, develop strategic account plans, and educate healthcare providers about bluebird’s gene therapy. This role involves collaboration with cross-functional teams to address account needs and enhance patient identification for treatment.
The Principal Data Engineer will design and implement end-to-end data workflows for ML modeling, improve model performance, and enhance data processing frameworks. Responsibilities include creating standards and best practices, ensuring data accuracy, and collaborating with data scientists to meet data needs.
The Compliance Manager (Director) will oversee compliance standards and ethics at Altos Labs, managing the implementation of policies, conducting risk assessments, overseeing investigations, and ensuring adherence to regulations. They will support the Chief Compliance Officer in developing compliance programs and provide training to stakeholders.
The Senior Scientist will lead analytical development for AAV gene therapy and manage quality control activities including assay development, regulatory documentation, and cross-functional collaboration. They will mentor team members and drive continuous improvement initiatives while adhering to industry standards and regulations.
The Research Associate in Histology will handle daily histology operations, such as setting up and breaking down equipment, performing histological techniques, maintaining accurate records, and supporting research activities in a laboratory setting.
The Group Copy Supervisor will lead the creative development of copy and content for pharmaceutical clients, collaborating with various teams and ensuring the alignment of creative work with brand goals. Responsibilities include managing projects, cultivating client relationships, and overseeing the editorial process, all while delivering quality work on tight deadlines.
The Staff Research Lead will oversee research projects in drug discovery, focusing on real-world data studies and patient-centric insights. Responsibilities include translating research questions into study designs, managing projects using agile tools, collaborating with cross-functional teams, and working with diverse data types using R and Python in cloud environments.
The Biomanufacturing Sales Lead is responsible for promoting and selling pharmaceutical devices to academic institutions and biopharma companies. Key tasks include leading a sales team, developing sales strategies, engaging clients, providing customer support, and conducting market research to identify new opportunities while building long-term relationships with clients.
Under moderate supervision, the Computer Operator II is responsible for monitoring computer systems and connected devices, managing report printing and distribution, troubleshooting issues, maintaining inventory of equipment, and ensuring an organized workspace. They also provide remote support and perform preventative maintenance on hardware.
As a Field Human Resources Manager, you will oversee HR functions at multiple Distribution Centers, coordinate with management on various HR tasks, manage associate relations, participate in recruiting, conduct training, and ensure compliance with HR policies and regulations.
The QRA Specialist monitors the compliance program, assists with inventory and safety compliance, tracks regulatory records, conducts internal audits, and helps maintain safety and security standards in the Distribution Center.
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