Biotech Manufacturing Process Validation Specialist Jobs

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8 Biotech Manufacturing Process Validation Specialist jobs found on Monster.

Jobs 1 to 8 of 8
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 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...
Bayer HealthCare (BHC), an Equal Opportunity Employer, makes an important contribution to human and animal health with its innovative products and by researching new therapeutic approaches promoting science for a better life throughout everything that we do. Our Specialty Pharmaceutical business ranks among the top 10 specialty pharmaceutical companies worldwide. Our global research and developmen...
Primary Role The individual will work in the Supplier QA sub-group of Shire Human Genetic Therapies Quality Assurance Department. This unit oversees contract manufacturing (3rd party manufacturing) operations, supply chain operations and supplier quality functions performed on behalf of Shire. This position supports the execution of quality systems including the external audit program. This positi...
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...
TechData is looking for Scientist I, Scientist II, Biostatistician (on site or telecommuting), SAS Programmer/Statistical Programmer/telecommuting, CDISC programmer (remote, multiple positions as sr. or lead positions), Java Programmer (Remote), Medical Writer, Sr. Clinical Data Manager, Drug Safety Specialist for our pharmaceutical clients in Central and Northern NJ. Please see below requirements...
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