- Takeda Pharmaceuticals (Boston, MA)
- By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application ... (Implementation guide) and FDA TCG (Technical conformance Guide); contribute to process improvement initiatives for creating standard outputs; review CRF designs to… more
- Bausch + Lomb (Greenville, SC)
- …using HPLC/UPLC and GC analytical equipment. Analytical method development, validation and transfer of stability indicating methodologies for actives, related ... and technician level personnel in support of chromatographic testing activities for pharmaceutical , vision care and eye care products. **Key Activities:** + Author… more
- Curia (Albany, NY)
- …Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. The Analytical Department is responsible for ... The routine functions of the laboratory are testing of raw materials, in- process , end product, and stability samples. The principal responsibility of the Research… more
- Boehringer Ingelheim (Ridgefield, CT)
- …for all study activities (tissue trimming through archiving), serving as the validation manager for all equipment and software used in the laboratory, as ... and techniques, and recommending and implementing new technology or process improvements aligned with business needs. * Demonstrates fiscal responsibility… more
- Convey Health Solutions (Fort Lauderdale, FL)
- …document resolutions. ESSENTIAL DUTIES AND RESPONSIBILITIES Enrollment Processing + Process queue items, inter-departmental and customer requests timely and ... Review and investigate returned checks, rejected ACH and credit card transactions + Process requests for automated premium payment via credit card or ACH withdrawal… more
- American Red Cross (Nashville, TN)
- …process improvements within area of responsibility. Lead suspect product/sample management process . + May participate in the validation of hardware, software, ... substituted). + Education: Bachelor's degree is a plus + Blood Bank or Pharmaceutical manufacturing experience is a plus. _BENEFITS FOR YOU:_ As a mission-based… more
- Abbott (Plymouth, MN)
- …device regulations and submissions. + Experience with risk management, design verification, or process validation work. + Proficient with MS Office suite (Word, ... with FDA submissions and applicable regulations. + Supports the product release process by creating GTS licenses or reviewing and approving requests for product… more
- Abbott (Sylmar, CA)
- …broad business needs. ensure compliance. + Cross-functionally lead Quality System process improvements which may include training, corrective action and preventive ... action (CAPA) activities, quality audits, validation . + Works under general direction; independently determines and develops approach to solutions; work is reviewed… more
- Teva Pharmaceuticals (Denver, CO)
- …Term Disability and more. **Make a difference with Teva Pharmaceuticals** **Reports To** In process of validation **Already Working @TEVA?** If you are a current ... + Bachelor's degree required + Minimum of 5 years of pharmaceutical sales experience required, preferably in the psychiatry or long-acting injectable… more
- Micron Technology, Inc. (Boise, ID)
- …by reviewing design performance and coordinating with vendors for equipment validation and system startup. + Offer technical mentorship to third-party designers, ... years, with 2 years coordinating third-party design for plumbing, HVAC hydronic, or process piping systems. + Strong knowledge of wet mechanical system design for… more