Lab Manager Salary at Receptos Inc BETA

Job Title: Lab/Engineering Technician Location: San Diego, CA (100% Onsite) Duration: 4 months- 6 months, possible extension Job Description: This role is with one of the Fortune 5 clients, and you’ll be working in the Cellular GNSS department. The primary responsibility will be providing lab support, including assisting with RF lab equipment, soldering rework, and general lab maintenance. Key Responsibilities: RF Lab Setup: Familiar with RF lab equipment and able to build test setups based on instructions. Rack Assembly Support: Assist in rack assembly based on provided instructions. Soldering Rework: Perform soldering rework on existing boards with 0201 components; RF experience is necessary. Lab Management: Handle and organize lab inventory, including heavy machines, soldering stations, setups, and cables. General Lab Support: Assist with various tasks related to lab management and support. Qualifications: Experience: Previous experience with RF lab equipment and soldering. Skills:

Job Title: Quality Control Specialist Location: San Diego, CA 92130 Duration: 6+ months Shift: 8-4:30 M-F Pay Rate: $28/hour on W2 Job Description: Must have: BA/BS degree in a related scientific discipline or some related college coursework with a minimum of 2 years’ experience in a biotech lab environment. The QC Associate I is responsible for routine, accurate and timely testing of QC samples according to standard protocols and operating procedures, such as flow cytometry related protocols. The QC Associate I will prioritize daily workload and work independently. They will participate in the review of data, report results, and complete all required documentation and database entries. QC Associate I will receive specific instructions and ongoing guidance regarding required tasks and expected results. Job Responsibilities • Trains and becomes proficient in all the required techniques, operation of relevant equipment and software packages associated with testing, data analysis, and dat

Role Overview: The Clinical Trial Manager (CTM) oversees the execution of clinical trials, ensuring data accuracy, protocol adherence, and timely study completion. This role involves coordinating with internal and external teams to drive the successful progression of studies. Key Responsibilities: Manage clinical studies across all phases of development. Contribute to the creation of key study documents (protocols, ICFs, CRFs, etc.). Develop recruitment and retention strategies for study participants. Oversee study document management, including regulatory and insurance requirements. Create training materials for teams, sites, and vendors. Share key study information with stakeholders through reports. Ensure compliance with ICH/GCP and relevant regulations. Assist with RFPs and vendor/CRO selection. Draft and negotiate contracts with vendors and sites. Collaborate with Regulatory Affairs to ensure GCP compliance. Identify risks and implement mitigation strategies. Develop and maintain

Job Description Job Title: Scientific Associate Chemistry Location: San Diego, CA Duration: 9 months contract with possible extension ONSITE POSITION Summary Job duties are listed below but not in order of requirement or necessity. The actual work that the new contractors perform will be based on what impact they can immediately make to overall synthesis processes. Synthesis Solution preparation Amidite preparation Column packing MM-12 and Akta synthesis Deprotection Transfer of support and subsequent deprotection Crude yield and LCMS characterization Purification and/or conjugation Buffer preparation Column packing or preparation Prep. Purification – anion exchange, reverse phase Akta’s and Agilent Prep Fraction analysis – LCMS and HPLC Yield quantification - UV Desalt – RPC, spin filter, TFF Post synthesis conjugation and purification Desalt Annealing of siRNA’s In-process analytical preparation and review during hybridization Operational General lab organization Ordering of consumab

Job Description Job Description Source One is a consulting services company and we’re currently looking for the following individual to work as a consultant with our direct client, a global pharmaceutical company On Site in San Diego, CA Candidates must be local to San Diego, CA with the ability to work onsite No C2C or sponsorship Title: Research Associate (Lab Sampling) Location: On Site San Diego, CA Contract Duration: 5 months, with likely extension Pay Rate Hourly: $30.00 w2 Monday - Friday, 40 hours weekly Job Description: The incumbent works closely with all functional areas in Research and Development, Manufacturing, Quality Assurance, Quality Control, Document Control and Regulatory Affairs. Basic understanding of the chemical and physical principals upon which formulation, process development and analytical methodology is based. Familiarity with concept of cGMPs. Basic skills in using typical laboratory and processing equipment (e.g. HPLC, UV Spec, pH meter, centrifuge, etc.)

Job Description Job Description Job Summary: You will perform QC testing and analysis on raw materials, in-process samples, and finished goods in a cGMP environment. Responsibilities include routine testing, data analysis, microbiology testing, maintaining lab inventories, equipment calibration, and ensuring lab cleanliness. The role also involves investigating assay issues, storing documents, and maintaining training records. Key Responsibilities: Conduct routine QC testing (GMP/GLP). Analyze data against specifications. Perform microbiology testing. Maintain inventories, lab cleanliness, and equipment calibration. Complete training and manage records. Participate in investigations for invalid assays and OOS results. 1-2 years of industrial lab experience (preferably in QC). Intermediate computer skills (Microsoft Office). Knowledge of GMP/GLP standards and industry regulations. Experience with ERP, LIMS, and/or QSR is a plus. Education: Bachelor’s degree in a science-related field.

Company Description: Abilita Therapeutics is an innovation-driven biotechnology start-up company focused on enabling the discovery and development of drugs targeting undruggable membrane proteins, including G Protein-Coupled Receptors (GPCRs), transporters and ion channels. With their technology, Abilita Therapeutics aims to discover and develop transformative antibody therapies to treat a wide range of diseases. For more detailed information, visit their website at www.abilitatx.com. Position Overview: We are seeking an experienced and dynamic PhD Scientist in Antibody Discovery to lead ambitious antibody discovery campaigns on several targets. The ideal candidate must have extensive expertise in yeast display and/or phage display. This role requires an individual that is passionate about antibody engineering and is willing to both plan and execute excellent experimental work. The candidate needs to be able to inspire a team of talented scientists focused on building a unique pipeline

Description Come join our exciting and fast-growing National Security Group! $15k SIGN ON BONUS! Must have an active TS/SCI Polygraph. We are hiring a Senior Windows Administrator / Test Lab Manager to join a high performing agile team using the Scaled Agile Framework (SAFe) methodology to support a highly complex and fast-paced program. The selected candidate will be responsible for performing daily system administration and O&M support activities in support of a complex network environment with geographically distributed systems. The position entails supporting system engineering requests to meet operational needs, as well as engineering, deploying, and maintaining capabilities that are new to the environment. Primary Responsibilities: The selected candidate will be responsible for monitoring test and development infrastructure systems, applications, and processes, and for ensuring that all issues are identified, tracked, and resolved in a timely manner. The environment includes Micr