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 (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.

Location (mandatory): Ontario, CAN L4A1H5 Small Description (mandatory): Manufacture products by operating equipment according to the Master Batch Record (MBR) in a pharmaceutical industry

Location (mandatory): Portsmouth NH Looking for a candidate with science degree and some manufacturing experience

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): Houston TX The Deviation Investigator/Initiator Level III is responsible for the initiation, investigation and completion of Minor and low/medium severity Major process deviations unassisted, and the supervised completion of high severity Major and Critical process deviations with the aim at identification of root cause, determining Product Quality Impact (PQI) and implementation of corrective actions to prevent recurrence.