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San Diego Biotech Jobs

San Diego, La Jolla, and Carlsbad biotechnology and life science jobs, updated with at least 5 new positions per day. Browse jobs, submit, get email updates.

Equipment Maintenance / Service Coordinator (CMMS)

May 7, 2015 – 1:22 am

CA-San Diego, Job Description: The manager is looking for candidates that are highly technical, preferably with experience in a CMMS (computerized maintenance management system) and other databases The system itself can be taught, but they need to have…

Technical Lead Software Test Engineer – Accelrys, Inc. – San Diego, CA

May 7, 2015 – 12:03 am

Our customer base includes the world’s largest pharmaceutical, biotechnology, chemical and petroleum companies….
From Accelrys, Inc. – 07 May 2015 07:03:47 GMT
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Account Manager – Genomics Solutions -San Diego

May 6, 2015 – 9:00 pm

Details: Company Overview As the world’s premier measurement company, Agilent works in close collaboration with engineers, scientists, and researchers around the globe to meet the communications, electronics, life sciences, and chemical analysis challenges of today and tomorrow. The company operates two primary businesses — electronic and bio-analytical measurement — supported by Agilent Laboratories, its central research group. Agilent is committed to providing innovative measurement solutions that enable our customers and partners– the leaders in their felds — to deliver the products and services that make a measurable difference in the lives of people everywhere. Learn More about Agilent Visit Our Company Website Sales: Responsible for generating existing and/or new Genomic product sales for assigned named accounts and/or within assigned geographic territory. Promotes and sells products and/or solutions to current or new customers/partners while keeping customers informed of new product introductions. Creates monitors and revises lead generation plans. Develops effective strategies and tactics enabling Agilent to gain market share. Responsible for developing customers and maintaining their satisfaction. Provide constructive feedback from customer into Agilent to help guide product development that effectively addresses customer needs. Maintains positive ongoing long-term relationships with key customers. • Proactively acts to understand customer needs and identify solutions to non-standard tasks/queries; actively creates business opportunities • Determines and develops approaches to sales assignments to achieve quota/ strategies • Solves a broad range of problems of varying scope and complexity

Director/AD, Clinical Data Management

May 6, 2015 – 9:00 pm

Details: BioPhase Solutions specializes in recruiting top talented professionals for San Diego’s Scientific community. We are currently looking for a Director/AD Clinical Data Management to work for a leading San Diego biotechnology company. Director/AD Clinical Data Management Provide operational expertise to the product/project teams under the guidance of the VP of Clinical Operations, having overall responsibility for the clinical data management function from the development of CRF’s though the final study report. The candidate will also build and lead the Data Management group to deliver high quality data, on time and on budget. Job functions Accountable for the clinical data management strategy and function, including determination of systems and processes for clinical trials, data management resourcing plan (vendors vs. consultants vs. internal staff), and development of oversight plan for outsourced activities Ensure that the Data Management group is aligned with business objectives and complies with FDA requirements Identify suitable vendor(s) for outsourcing data management activities and coordinate the review and approval of contracts Work closely with CROs to prepare and ensure proper execution of data management plans Manage data management projects from beginning to end Work closely with Clinical Operations, statisticians, SAS programmers and other staff as appropriate to develop CRF’s to ensure the required information for statistical analysis is present Coordinate with SAS programmers to create and validate database design and edit check specifications Communicate with all departments regarding project status/issues, provide ongoing feedback on data management workflows to increase efficiency and provide feedback to CRAs, both internal and external to the Company Oversee hiring, daily management, training and development of data management staff Ensure coding of safety data is accurate using industry standard coding conventions Oversee interactions with outside vendors (e.g. clinical laboratories) on collection, transmittal and transfer of study specific data Develop and update SOP’s associated with the data collection, handling and review processes to meet regulatory compliance and operational needs Assist with the validation of the statistical output for final reports Manage multiple and varied tasks, prioritize workload with attention to detail Oversight of internal staff and external Data Management CROs to ensure that data and documentation are delivered on time, on budget and to La Jolla’s quality standards Develop metrics to evaluate Data Management CRO performance, and determine actions taken to remedy or improve performance Development, maintenance and governance of CDM standards (custom eCRF, CDASH, etc.) Ensuring data management activities are conducted in accordance with GCP, GCMP, internal SOPs and meet all regulatory requirements Provide Data Management expertise to teams and other Data Management staff in identifying opportunities for process and budgetary optimization Innovate at the speed of technology to identify and implement emerging new ways of doing CDM as appropriate

Sr. Director, Clinical Development

May 6, 2015 – 9:00 pm

Details: The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, genetic information or any other characteristic protected by law. I…

Software Quality Engineer

May 6, 2015 – 9:00 pm

Details: PSC Biotech has an immediate need for a Software Quality Engineer in the San Diego Area The SQE candidate must have 5+ years’ experience and must possess solid understanding of FDA guidelines and industry best practices for this field. Responsibilities Basic Function and Scope of the Position: Responsible for providing software quality leadership, subject matter expertise and support to product development teams, manufacturing operations, and information systems in support of corporate production and quality objectives. This role requires exceptionally strong communication, interpersonal and organizational skills and a solid understanding of the application of FDA and ISO 13485 standards. The ideal candidate will have experience with process software and the IVD industry. Tasks and Responsibilities: • Provide quality oversight to Software Development and Software Verification & Validation Program • Provide guidance, review and approval of various project deliverables based on procedural requirements: o Design History Documents o Quality oversigth and review of Custom Process Software Packages o MES experience o Requirements Documents (User and Functional) o Review Software protocols o Traceability Matrices o Serve as Quality core team member on project teams • Ensure establishment and compliance to software risk management process throughout product lifecycle • Provide review and approval of software related change orders • Ensure successful transfer of software from development into production use • Provide quality assurance guidance on CAPAs as related to software • Provide leadership in the design and methods for measuring effectiveness (internal and external audits) and quality of process improvements related to software • Work with key partners to ensure global awareness and adherence to policy and procedures • Develop and deliver training to employees on software validation, software risk management, and general quality tools • Establish and monitor process metrics and develop action plans as needed • Represent area as a subject matter expert in support of audits • Provide management with plans and status updates on assigned responsibilities and goals • Other activities as assigned. All listed tasks and responsibilities are deemed as essential functions to this position; however, reasonable accommodations will be made if at all possible under business conditions. Applicant will be working in a biotech/pharmaceutical environment as a consultant/contractor for various clients of PSC. He/she will be working closely with client’s employees on various projects and various GMP facilities to help client with validation issues. Work is interesting and involves the ability to deal with and interpret technical information for the benefit of the client. Applicant must be knowledgeable in dealing with and keeping proprietary information confidential.

Cell Culture / Cell Based Assay Associate (San Diego)

May 6, 2015 – 5:45 pm

We are seeking a Cell Based Assays Associate to establish and maintain multiple mammalian cell lines. Seeking 5 years experience with cell based assays, luciferase assays OR proliferation assays, immunoassays (ELISA), establishing cell lines, freezin […

Cell Culture / Cell Based Assay Associate (San Diego)

May 6, 2015 – 5:45 pm

We are seeking a Cell Based Assays Associate to establish and maintain multiple mammalian cell lines. Seeking 5 years experience with cell based assays, luciferase assays OR proliferation assays, immunoassays (ELISA), establishing cell lines, freezin […

Research Scientist: Nanoparticle Formulation and Conjugation – Sorrento Therapeutics, Inc. – San Diego, CA

May 6, 2015 – 5:27 pm

Is a fast growing, clinical stage biotechnology company developing anti-cancer therapies ranging from small molecules to biologics, such as monoclonal antibody,…
From BioSpace.com – 07 May 2015 14:49:44 GMT
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Director of Microbiology Markets – Illumina, Inc. – San Diego, CA

May 6, 2015 – 5:05 pm

Our customers include a broad range of academic, government, pharmaceutical, biotechnology, and other leading institutions around the globe. All About Us….
From Illumina, Inc. – 07 May 2015 00:05:52 GMT
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