- Catalent Pharma Solutions (Kansas City, MO)
- **Controlled Substance Specialist II** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose ... service to pharma, biotech, and consumer health customers, supporting product development , launch, and full life-cycle supply. With time-tested experience in … more
- Catalent Pharma Solutions (Kansas City, MO)
- **Senior Validation Specialist I, BioAnalytics Computer System Validation (CSV) & Compliance** **Position Summary:** Catalent, Inc. is a leading global contract ... development and manufacturing organization (CDMO) whose mission is to...Kansas City, MO (KCM) is hiring a Senior Validation Specialist I, BioAnalytics CSV & Compliance. The Senior Validation… more
- Catalent Pharma Solutions (St. Petersburg, FL)
- …an understanding of document change control procedures, computer systems, and manufacturing process knowledge within a cGMP environment. Your talents, ideas, and ... **Documentation Specialist ** **Position Summary** Catalent, Inc. is a leading...**Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to… more
- Colgate-Palmolive (Topeka, KS)
- …Analytical program goals. + Conventional and rapid on-line/in-line/at-line methods for process monitoring, control, and release of raw materials, premixes, and ... in quality audit programs internally and externally + Support the development , implementation, and ongoing maintenance of Hill's rapid method analysis program… more
- Catalent Pharma Solutions (Manassas, VA)
- **Quality Assurance Specialist I - Quarantine** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization ... service to pharma, biotech, and consumer health customers, supporting product development , launch, and full life-cycle supply. With time-tested experience in … more
- Catalent Pharma Solutions (Greendale, IN)
- **Quality Specialist I** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to ... service to pharma, biotech, and consumer health customers, supporting product development , launch, and full life-cycle supply. With time-tested experience in … more
- Genentech (Hillsboro, OR)
- …and framework of one or multiple programs within HTO Quality in the areas of process development , process improvement, quality and compliance. You will own ... at the site and within the company network. + You will support internal cGMP audits and Health Authority inspections as a technical resource and quality subject… more
- Catalent Pharma Solutions (Chelsea, MA)
- **Quality Assurance Specialist II, Operations** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization ... to pharma, biotech, and consumer health customers, supporting product development , launch, and full life-cycle supply. With time-tested experience...SD1, SD4 and SD7, the latter being the largest CGMP unit of its kind for DPI in North… more
- Merck (Rahway, NJ)
- **Job Description** **Senior Specialist , Small Molecule Analytical Research & Development ** Small Molecule Analytical Research and Development (SMAR&D) team ... has an opening for a Senior Specialist in our SMARD GxP Operations team based in...work collaboratively with colleagues in Pharmaceutical Operations and Global Development Quality to ensure timely release of raw materials… more
- Curia (Rensselaer, NY)
- Curia Global Inc. (Rensselaer, NY) seeks a Quality Assurance Specialist II for its Rensselaer, NY location. The position is responsible for assisting with validation ... QA/QC in Validation and Quality Assurance-related issues. Specifically, the Quality Assurance Specialist II will perform the following duties: * Develop and maintain… more