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Location: 100% Remote Designs, develops, installs, tests, and documents complex application software including server, client, and web-based components. Contributes to the design and delivery of technical architecture solution components and provides technical guidance to less experienced personnel. May provide technical consulting support on complex initiatives while ensuring adherence to industry and organizational standards.
Location (mandatory): Tuczon, AZ Small Description: Supports the functions of RTD histology laboratories in the performance of routine histotechniques Physical conditions and PPE requirements: The physical demands described are representative of those that must be met by an individual to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. • Required to stand, walk, sit, kneel, bend, crouch for a combined 4 or more hours per day. • Required to push, pull, and lift a minimum of 25 pounds. Repetitive, consistent movements of the wrists, hands, and/or fingers. • Required to have good near visual acuity to perform activities throughout the processes in the assigned area. • This is an essential position supporting the organizational goals requiring attendance on weekends, holidays and during emergency or exceptional conditions The Opportunity • Prepare tissue samples for microscopic examination • Operate and maintain histology laboratory equipment • Ensure quality control and compliance with laboratory standards • Assist pathologists with specimen analysis • Follow safety protocols and regulatory guidelines Who You Are • 0–5 years of experience • Strong problem-solving skills • Excellent communication abilities • Knowledge of industry best practices Preferred (Optional) • Certification in histotechnology preferred
Location (mandatory): Tuczon, AZ Small Description: This onsite Research Associate II position in Oncology Assay Development focuses on designing and executing laboratory experiments to support assay and product development.
Small Description: Reporting to the Operations Lead, the Facilities Maintenance Specialist plans, oversees, and executes maintenance activities at the Client Life Sciences Center (ALSC). The role involves routine, planned, and reactive maintenance, project-based activities, vendor coordination, and ensuring compliance with all applicable regulations and policies.
Location (mandatory): Tuczon, AZ (Remote, just 1-2 times in office/month) Small Description: The Technical Writer will be responsible for creating, reviewing, revising, and finalizing high-quality documentation and labeling products. This role serves as a key point of contact between project teams and the Technical Documentation Department, ensuring timely delivery of compliant documentation in alignment with project schedules and regulatory standards. The writer will also support departmental tools, processes, and corporate standards. Work Arrangement: • This is a remote position. • Local candidates are preferred and will be required to visit the office 1–2 times per month for initial team integration and collaboration.
Location : Colorado Springs, CO 80915 The Shipper will be responsible for handling, preparation, and all details pertaining to ship various products, under minimum supervision. In this role, the incumbent will also perform loading the cargo into/onto various types of trucks, forklift and packaging experience preferred. Small parcel packaging along with label preparation and email and computer competency a must.
Small Description: We are seeking candidates with experience in managing a caseload of first-party property claims across various home types, including traditional homes, mobile homes, and condominiums, within a standard authority limit. Responsibilities include making coverage decisions, assessing and valuing damages, and interacting with policyholders, public adjusters, attorneys, and other third parties throughout the claims management process. Candidates must adhere to state compliance requirements and company guidelines for claims handling.
Location (mandatory): Menlo Park, CA • Despite rapid advancements in generative AI, achieving high-quality generation remains a challenge. This is primarily due to the scarcity of high-quality training data and the lack of reliable and robust evaluation metrics that can effectively capture subtle details in model outputs, which can significantly impact user experience. • Our team is dedicated to developing comprehensive data curation and evaluation solutions to enhance our model across various quality dimensions. These include visual quality, prompt adherence, identity preservation, naturalness, and visual text generation, among others. We employ diverse approaches, such as sourcing billions of images and identifying suitable ones through a combination of manual annotations and signals from machine learning models. We also utilize both manual and automated evaluation methods to pinpoint quality gaps and data requirements.
Location (mandatory): Vacaville California With limited supervision, QC Associate I, is responsible for the performance of direct materials testing in accordance with cGMP regulations. These duties include execution of laboratory testing, trend analysis, documentation review, support of discrepancies (OOS, OOT, OOE) and other laboratory support activities. In conjunction with Quality Control leadership, the QC Associate II works to meet departmental and organizational goals.
Location (mandatory): Vacaville CA The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level I associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials.
Location (mandatory): Houston TX The Environmental Monitoring (EM) Core Technician will be responsible for conducting EM tasks in support of production and aseptic processing of clinical grade products. The core tech will also be responsible for maintaining, stocking, and set-up of clean room environment.