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.

Location : Remote We are seeking a detail-oriented and innovative Marketing Healthcare Writer to join our team. This role focuses on creating accurate, engaging, and compliant digital content for diverse promotional channels within the healthcare sector. The ideal candidate will collaborate closely with the marketing team and leverage AI-driven tools to streamline content development while ensuring quality and compliance

Location : Portsmouth NH Validation Engineer II responsible for Computer System Validation (CSV) in a regulated biotech/pharma manufacturing environment, ensuring GMP compliance for automation, process control, and MES systems while supporting site and process improvement initiatives.

Location: Rockford, IL 61103 Performs a variety of laboratory tasks under the supervision of a Scientist/Researcher. The technician will use both standard procedures and adapted processes to support specific projects and routine operations, while collaborating with maintenance staff to ensure smooth equipment functioning.

Location : Sanford, NC. The Specialist, QA Validation will be primarily responsible for the implementation, execution and assessment of quality systems, procedures, and records to support compliant GMP operations. This position works closely with Validation, Engineering, Manufacturing, Quality Control, Facilities, and Automation.