Location: 4745 Wiley Post Way Salt Lake City, UT 84116 Small Description: This is an entry level position. Shift Schedule: Monday - Friday 8:00am - 5:00pm. Job ID: TEVAJP00009751. Performs testing of raw materials and drug products, maintenance and calibration of analytical instruments, prepares standard and sample solutions and maintains appropriate records. Focus on candidates who have hands-on bench and laboratory experience (including academic or internship lab work), with exposure to sample preparation, routine testing, and documentation in a lab setting. Prioritize early-career profiles, such as associate-degree level candidates or students currently in school or taking a short break.

Location (mandatory): 66 Hudson Yards Blvd East, New York, NY 10001 (Hybrid) Small Description: This is a full-time, 12-month Contractor/Research Associate (RA) position on the HTA, Value & Evidence (HV&E) Thoracic & Precision Medicine Oncology team within the Global Access & Value (GAV) organization. The Research Associate will provide technical support, analysis, and reporting for assets at various stages of development within the Economics and Outcomes Research (HEOR) function. Interview Schedule: Two rounds of interviews will be conducted: an initial screening interview followed by a team interview.

Health Care Copywriter (Digital & Media Content) This fully remote role is for a Health Care Copywriter who creates compliant, engaging digital and media content for both HCP and consumer audiences. You’ll translate clinical data and approved claims into clear messaging across ads, social, emails, video scripts, and partner platforms, while working closely with designers, marketers, and regulatory teams. The job requires 3+ years of healthcare copywriting experience, comfort with MLR processes, attention to detail, and the ability to leverage GenAI tools to accelerate content without compromising accuracy or compliance.

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.

Location : Gold River, CA 95670 (Hybrid) AWS Cloud Engineer at company, you can contribute your skills as we harness the power of technology to help our clients improve the health and well-being of the members they serve — a community’s most vulnerable. Connect your passion with purpose, teaming with people who thrive on finding innovative solutions to some of healthcare’s biggest challenges. Here are the details on this position.

Location (mandatory): Roseville, MN 55113 Laboratory Technician to join our team for a second-shift position. The successful candidate will receive training during the first month to six weeks on the first shift before transitioning to the second shift (1:30 PM - 10:00 PM). In this role, the candidate will be responsible for managing hazardous waste and industrial wastewater, as well as overseeing QA/QC processes for the materials being produced.

Location (mandatory): Salt Lake City, UT, USA 84116 (On-site) Small Description: Performs testing of raw materials and drug products, maintenance and calibration of analytical instruments, prepares standard and sample solutions, and maintains appropriate records.