- Curia (Albuquerque, NM)
- …where our work has the power to save lives Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering ... with pharmaceutical and biotech companies to provide life-saving treatments to...to support validation conclusions. + Read/interpret SOPs to ensure compliance + Maintain up to date trainings + Other… more
- Cambrex High Point (Longmont, CO)
- Company Information You Matter to Cambrex. Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug ... small and large molecule development and testing data in compliance with cGMP/cGLP standards and FDA / EU regulations....requirements and implementation for GLP and GMP in the pharmaceutical industry + Effective team and interpersonal skills with… more
- Curia (Albuquerque, NM)
- …global contract research and manufacturing services to the pharmaceutical and biotechnology industries. Summary: The lyophilization department is responsible for ... operate lyophilizers according to specifications, monitor cycles, review data for compliance , and complete necessary documentation. Cleaning operations occur in a… more
- Charles River Laboratories (Wayne, PA)
- …and salary reviews. + Develop and maintain departmental systems and SOPs. Maintain compliance of operating documents through review and revision as required by SOPs. ... Working knowledge of cGMPs or regulatory requirements pertaining to the pharmaceutical and biotechnology industries required. **PHYSICAL DEMANDS:** + May have… more
- Sumitomo Pharma (Morrisville, NC)
- Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... drive profitable growth, including developing financial models related to providing contract manufacturing support to internal and external partner organizations. +… more
- Curia (Albuquerque, NM)
- Job Title: Microbiologist III, Albuquerque, NM Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology ... as water, steam, nitrogen, etc. * Perform environmental monitoring of cleanrooms in compliance with USP and EU specifications. * Review, trend, and report results… more
- AbbVie (Mettawa, IL)
- …standards for their department designed to reduce cycle time, maintain compliance and improve productivity. Responsibilities: * Responsible for leading the Europe ... related groupings, who in turn, directly oversee individual contributor site contract managers, with responsibility for negotiating contracts and budgets with… more
- Endo International (Rochester, MI)
- …products, including Par branded, development and generic as well as contract customer products while meeting department quality, safety, delivery and productivity ... products, including Par branded, development & generic as well as contract customer products while meeting department quality, safety, delivery and productivity… more
- Charles River Laboratories (Ashland, OH)
- …with a Master's degree, 0 to 2 years with a Ph.D.; in the contract research, academic, or pharmaceutical industries. + An equivalent combination of education ... interpretation, and reporting of study data, and assuring the regulatory compliance of these projects. **ESSENTIAL DUTIES AND RESPONSIBILITIES:** + Efficiently… more
- Fujifilm (Morrisville, NC)
- …Procurement leadership experience should include sourcing, supplier selection, risk and compliance evaluation, contract negotiation and financial analysis + ... Manager focuses on maximizing value, optimizing processes, and ensuring compliance with procurement standards. **Company Overview** At FUJIFILM Diosynth… more