Biotech Manufacturing Process Validation Specialist Jobs

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6 Biotech Manufacturing Process Validation Specialist jobs found on Monster.

Jobs 1 to 6 of 6
Auto req ID: 2002BR Job Posting Title: Validation Specialist Person Type: Regular Posting Category: Industrial Operations & Product Supply Location: Rensselaer Job Summary and Essential Functions: Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the t...
Job Details: Validation Engineer - commissioning - qualification "Experience with biotech (cell culture, bioreactors, filters, centrifuges, chromatography/purification, water for injection, clean steam, autoclaves)" W2 rate with a $4100.00 a month per diem Skills and Knowledge: Facility qualification / validation and must understand commissioning / qualification and adhere to validation and qualit...
Job Description Posting date: May 2, 2014 Position Summary: The Field Applications Specialist (FAS) primarily interfaces between the Commercial Sales Organization (Account Managers), the internal source base within the Company, possible third party partners/suppliers and the end-user/Customer. The FAS will ensure optimal utilization of appropriate Single-Use Systems technologies, products and serv...
Summary Description: The Calibration Specialist will be responsible for the performing calibration and validation on all equipment in our Memphis, TN manufacturing facility. The Calibration Specialist will inspect, test, adjust, and calibrate instruments. The Calibration Specialist will be expected to supply instrument calibration to insure reliability of instruments and measurements. Duties: oDev...
Auto req ID: 2121BR Job Posting Title: Analytical Specialist Person Type: Regular Posting Category: Industrial Operations & Product Supply Location: Rensselaer Job Summary and Essential Functions: Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the t...
Purpose / Summary Provide managerial leadership to ensure the safe, compliant and cost effective management and administration of engineering department documentation in support of LMI facility, process, and manufacturing operations. Is Accountable to independently plan, organize, lead and control all aspects of ownership of LMIs engineering documentation. This role exhibits the competent leadersh...
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