Pharmaceutical Biotech Engineer Validation Specialist Jobs

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14 Pharmaceutical Biotech Engineer Validation Specialist jobs found on Monster.

Jobs 1 to 14 of 14
Baxter International Inc Los Angeles, CA
Description Applies a solid understanding of theories/practices utilized by other disciplines outside the primary area of expertise toward the development of new or enhanced products or processes. Plans, executes, and functionally directs important engineering assignments, which require independent judgment. The position also requires expertise in validation theory and principles such as process ...
Baxter International Inc Los Angeles, CA
Description The Sr. Validation Specialist responsibilities will focus on Facilities, Process and Equipment Validation, using knowledge and experience with Equipment and Processes typically used in Biotechnology and Pharmaceutical Manufacturing. Typical facilities and equipment used includes critical utilities, ISO 8 manufacturing space, Vessels, Filtration skids, UF/DF skids, CIP/COP systems, h...
TechData Service has multiple contract positions open with many top pharmaceutical companies along with home based positions for job titles including Training Specialist, QA/QC Specialist III, Clinical Documentation Specialist, GRA CMC Manager, Lead Data Manager, Clinical Data Analyst II, Clinical Trial Associate II, Associate Director, Scientific Communications, Change Management / Project Manage...
Facility And CAD Technologies, Inc. is a small, privately owned business providing crucial CAD and Document Management services to Life Science companies in southern California. Some of our clients are seeing rapid growth in their manufacturing operations, driving increased demand for our services. To meet this need, we are actively recruiting for a Facilities Engineering CAD Specialist to join ou...
TechData is looking forBiostatistician (remote) and SAS programmers (Some positions can be telecommuting), SAS/Statistician/Remote, Network engineer, Trial Supplies Operations Manager, Technical Writer, Clinical Compliance Specialist, Project Manager/IT for our pharmaceutical clients. Please see below requirements and send your resume to: *****. TechData is a leading provi...
Operations Automation Engineer II/Mfg. Technical Specialists III Automation Technology Requisition ID -2961699331 The Position Summary Responsible for executing Automation technical support and engineering activities for GMP Manufacturing Operations in a multi-product, large scale, automated biopharmaceutical facility. This includes activities related to safety, compliance, quality, staff dev...
Operations Automation Engineer II / Mfg. Technical Specialist III - AutomationTechnology Requisition ID -2961699231 The Position Summary Responsible for executing Automation technical support and engineering activities for GMP Manufacturing Operations in a multi-product, large scale, automated biopharmaceutical facility. This includes activities related to safety, compliance, quality, staff d...
Description Summary Responsible for executing Automation technical support and engineering activities for GMP Manufacturing Operations in a multi-product, large scale, automated biopharmaceutical facility. This includes activities related to safety, compliance, quality, staff development, targeted innovation, and plant performance and success. Deliverables include but are not limited to leading ...
Description Summary Responsible for executing Automation technical support and engineering activities for GMP Manufacturing Operations in a multi-product, large scale, automated biopharmaceutical facility. This includes activities related to safety, compliance, quality, staff development, targeted innovation, and plant performance and success. Deliverables include but are not limited to leading ...
Automation Engineer DCS/MES Requisition ID-3088879118 Description The Position: Exciting position supporting Manufacturing Control Systems (DCS and MES) for cell culture operations in state of the art biotech facility. Support for major plant expansion to increase Vacaville site capacity making it the largest biotech manufacturing facility in the world. Come be part of the team that will make ...
Description The Position: Exciting position supporting Manufacturing Control Systems (DCS and MES) for cell culture operations in state of the art biotech facility. Support for major plant expansion to increase Vacaville site capacity making it the largest biotech manufacturing facility in the world. Come be part of the team that will make a significant impact on bringing medicines to patients. ...
Role Summary/Purpose This role will provide the formal technical and clinical support during the sales process for our manufacturing equipment within a limited geographic region supporting BioProcess Sales. Responsibilities span across the full equipment sales cycle, from initial customer contact through installation, training and/or customer service activities in support of sales objectives for ...
VWR International , Inc. Raritan, NJ
Lab Support Specialist Physical Location: Greater Raritan Area Location: VWRCatalyst - VWRCatalyst Location City: Raritan Department/Function: VWRCATALYST State/Territory/Province: US-NJ Last updated: 2/26/15 9:14 AM Description VWR (NASDAQ: VWR), headquartered in Radnor, Pennsylvania, is a leading, independent provider of laboratory products, services and solutions with worldwide sales in ex...
Sr. Mgr. Regulatory Affairs (Animal), Project Manager, Sr. Consultant (GMP/MFG), Business Process Analyst, Technical Writer Scientific Baltimore, MD
Apply Now ? Apply to this Job Attach your resume By providing us with your information, you agree to become a Bullhorn Reach User, and to our use and disclosure of your information as described by our Privacy Policy. Job Description Job 1 - Senior Specialist, Regulatory Submissions Management - Manufacturing Change & Compliance (Animal Studies) (3yrs to 10yrs) Project Managing and/or Leadin...

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