- Aequor (Vacaville, CA)
- …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.Job Responsibilities Perform a broad… more
- ALPCO (CA)
- …business model. ALPCO’s portfolio is derived from internal R&D and cGMP manufacturing, as well as externally sourced products offered as OEM ... “ALPCO-branded” kits or distributed under the original manufacturer’s label.Position OverviewThe successful candidate is highly motivated, adaptable, and thrives in a fast-paced environment. This role combines technical field service expertise with… more
- Takeda Pharmaceutical (Los Angeles, CA)
- …responsible for executing all processes in production while strictly adhering to cGMP , environmental health and safety guidelines and any other related regulations ... How you will contribute: Follow all safety rules, SOPs, cGMP , work rules and other company policies and...English (both verbal and wr itten) and understanding of cGMP regulations in a pharmaceutical manufacturing environmen t. Must… more
- Takeda Pharmaceutical (Los Angeles, CA)
- …Operating Procedures (SOP) to ensure compliance with FDA guidelines, QSR, cGMP , and other regulatory standards and drive procedural improvements. Support internal ... Degree in Chemistry or Biological Science is preferred. Strong knowledge of cGMP , QSR, USP, CFR, and other regulatory requirements. Demonstrated working knowledge of… more
- Takeda Pharmaceutical (Los Angeles, CA)
- …pumps, industrial control systems as responsibilities assigned to Refrigeration in both cGMP and non- cGMP areas Responsible for repairing refrigeration systems, ... low, medium and normal temperature, cold storage equipment, building automation system components, mechanical and electrical equipment as assigned. Must be familiar with plant and divisional SOP's as related to positional and department responsibilities.… more
- Takeda Pharmaceutical (Los Angeles, CA)
- …with minimal guidance. Able to prioritize multiple tasks. Able to incorporate cGMP concepts, quality systems requirements and safety into process and equipment ... design. Must be able to provide solutions that reflect an understanding of business objectives and cost implications. Important Considerations: At Takeda, our patients rely on us to deliver quality products. As a result, we must follow strict rules in our… more
- Eckert & Ziegler Isotope Products, Inc. (Valencia, CA)
- …(EU 2017/745) CE Mark compliant Quality Management System. Manages and conducts cGMP and employee trainings. Maintains additional quality systems and compliance as ... required. Oversees the Regulatory Compliance Program, Corrective Action & Prevention Action (CAPAs) Program and the Internal Audit Program. Conducts internal and supplier audits, writes audit reports, issues CAPAs and trains internal auditors to conduct these… more
- University of Southern California (Los Angeles, CA)
- …what it is. USC's Keck School of Medicine, current Good Manufacturing Practices ( cGMP ) facility is seeking a dynamic individual to work on the process development ... and gene therapies and other biological products for internal/external users. The cGMP Process Development (PD) Specialized Lab Technician at the USC/CHLA cGMP… more
- University of Southern California (Los Angeles, CA)
- …of internal/external users in the university's current Good Manufacturing Practices ( cGMP ) facility. The Quality Control (QC) Specialist is responsible for ... be responsible for ensuring consistency with current Good Manufacturing Practice ( cGMP ) principles. Job Accountabilities: + Supports cGMP manufacturing… more
- University of Southern California (Los Angeles, CA)
- …staff that make the university what it is. USC's Keck School of Medicine, cGMP Department is seeking a dynamic individual to foster and enhance the translation and ... biological products for internal/external users. The Associate Director of Process Development ( cGMP ) is responsible for all aspects of operations related to the… more
