- Lilly (Indianapolis, IN)
- …the world. **Organization Overview:** Join the energetic and growing Active Pharmaceutical Ingredient - External Manufacturing Organization (API-EM) that delivers a ... reliable and compliant manufacture of API drug substance at external contract manufacturing groups to predetermined global quality standards. This person interacts… more
- Omaha Children's Hospital (Omaha, NE)
- …various programs. * Assists in researching products, prices and maintaining contract compliance Leads the implementation, maintenance and compliance monitoring of ... documentation including receipt, pricing and terms. * Ensures multistep receipt validation and documentation of each inventory item. * Resolves invoice discrepancies… more
- Lilly (Indianapolis, IN)
- …capacity expansions and line extensions for IDM at Lilly sites and Contract Manufacturing receiving sites across the globe. IDM Asset Delivery Process Engineers ... automated device assembly equipment for IDM globally to both Lilly sites and Contract Manufacturers. In addition, when primary support teams for the global installed… more
- Honeywell (Baton Rouge, LA)
- …quality and regulatory standards. The GMP QA Manager also monitors Contract Manufacturing Organizations (CMOs) ensuring compliance of the manufacturing, packaging ... and analytical testing of pharmaceutical dosage forms and drug substances. They also identify...quality of intermediates, drug products + Reviews and approves validation protocols and reports, Specifications, certificates of analysis (CoAs),… more
- System One (Cambridge, MA)
- Job Title: Bench Scientist Location: Cambridge, MA Type: Contract Overview Leading pharmaceutical company looking for an experienced Bench Scientist. Ideal ... or a Masters degree with 3+ years of experience in Assay Design/ Validation , ELISA and more. Responsibilities Seeking a highly motivated scientist with experience… more
- Teva Pharmaceuticals (Forest, VA)
- …set-up and qualification. * Responsible for supporting validation /qualification activities (process/equipment/facility). * Responsible for developing, transferring ... microbial organisms. * Responsible for preparing samples for shipment to contract labs as applicable. * Responsible for drafting/amending Standard Operating… more
- Lilly (Branchburg, NJ)
- …operations. This position will interact with the manufacturing, engineering, validation , quality control and regulatory departments. Interaction may be required ... with other Lilly site / contract producers of Lilly products. The Quality Professional works...meetings to provide compliance guidance to Manufacturing, Laboratories, Maintenance. Validation or supporting business units. + Ensure compliance with… more
- Two95 International Inc. (Durham, NC)
- …(small molecules), Ph.D. with 5-7+ years. + Excellent method development and validation skills and routine analysis on pharmaceutical materials (including potent ... + Strong preference for an analytical scientist who either has worked within a contract analytical lab working with external clients or has worked within a pharma… more
- Charles River Laboratories (Mattawan, MI)
- …studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and ... sample analysis studies with oversight + Assist in execution of method validation projects with oversight as needed + Operate laboratory instruments with complete… more
- Charles River Laboratories (Mattawan, MI)
- …these platforms/assays, the teams are responsible for the method development, validation and routine samples analysis in both the regulated and non-regulated ... sample analysis studies with oversight + Assist in execution of method validation projects with oversight as needed + Operate laboratory instruments with complete… more