- CBRE (Luquillo, PR)
- …or lab facilities which may include biology, cell/gene therapy, chemistry, pharmaceutical , cGMP process manufacturing, agricultural / food science, vivarium, ... and production areas thus the candidate should be familiar with pharmaceutical current good manufacturing practices (cGMP) including commissioning processes. The… more
- Sanofi Group (Framingham, MA)
- …responsible for providing Facilities, Engineering and Maintenance support for all cGMP process and utility systems at Framingham MA Campus, maintaining these systems ... in a validated state of control and ensuring uninterrupted business continuity. This organization is also responsible for shared GMP and non GMP systems on the… more
- Sacramento County (Sacramento, CA)
- …intermittent on-call. Under direction, the Pharmacist compounds and dispenses pharmaceutical drugs, medicines and prescriptions, and provides direct consultative ... drug therapy. Examples of Knowledge and Abilities Knowledge of + Pharmaceutical arithmetic, chemistry, materia-medica, and pharmacology + Pharmaceutical … more
- Catalent Pharma Solutions (Greendale, IN)
- …IN. **The Role** + Own and manage site-level quality systems such as: Change Control and Deviation processes in accordance with internal procedures and ... or dietary supplement industry experience preferred. + Strong working knowledge of Change Control , Deviation, and CAPA processes. + Experience with TrackWise,… more
- Sanofi Group (Swiftwater, PA)
- …include project scope related to manufacturing process equipment, automated control systems, change control development and execution, commissioning ... a leadership role in identifying and resolving issues related to manufacturing process equipment and/or automated control systems for Continuous Improvement… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- …+ Provide guidance and work with stakeholders from various departments to process Investigations, CAPA, Change Controls, Deviations + Coordinate and collect ... the elements of the Quality Systems including, but not limited to: Change Controls, Quality Events, Deviations, Corrective and Preventative actions, QMR, Risk… more
- Actalent (Sanford, NC)
- …BasedJob Description The Sr. Associate Scientist will support the Quality Control Method Transfer and Validation team by performing method validation activities, ... Engage with the method development team and participate in in- process and final product sample analyses. + Author relevant...deadlines. Essential Skills + Experience with GMP in a pharmaceutical lab environment. + Proficiency in PCR or ELISA… more
- HCA Healthcare (Kissimmee, FL)
- …and availability of stocked medications + Is responsible for the new drug addition, change , deletion process and monitors compliance with process + Evaluates ... the hospital and non-hospital accounts + Is responsible for the new drug addition, change , deletion process and monitors compliance with process +… more
- Novo Nordisk (Clayton, NC)
- …for millions of people around the world. In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our ... injectable and oral treatment supply chains. Our newer Active Pharmaceutical Ingredients (API) facility in Clayton, NC sits on 825,000 square-feet of… more
- Lilly (Lebanon, IN)
- …direction and provide oversight for setting the technical agenda to improve process control , yield, and/or productivity. + Ensure adequate oversight and ... and complaints. + Ensure adequate oversight for technical projects to improve process control , capacity, yield, quality. + Ensure adequate technical… more
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