Pharmaceutical Biotech Engineer Validation Specialist Jobs

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15 Pharmaceutical Biotech Engineer Validation Specialist jobs found on Monster.

Jobs 1 to 15 of 15
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, heat exchanger...
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...
We have an available opportunity for a Validation Manager in the New England / Boston area. This opportunity is with a nationwide company that is well established, and growing. The ideal candidate will have over 10+ years of experience, and a solid background in the pharmaceuticals industry. This is a direct hire position. Salary+Benefits. We are looking for someone who is committed, and can cont...
We have an available opportunity for a Validation Project Manager in the Los Angeles area. This opportunity is with a nationwide company that is well established, and growing. The ideal candidate will have over 10+ years of experience, and a solid background in the pharmaceuticals industry. This is a direct hire position. Salary+Benefits. We are looking for someone who is committed, and can contr...
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 validation, c...
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 ...
AstraZeneca West Chester, OH
POSITION SUMMARY: Manage the design, implementation, and support for Plant-Wide Process Automation (PA) and Supervisory Control and Data Acquisition (SCADA) solutions within the Hamilton, OH facility used to support pharmaceutical development and manufacturing. Manage activites of 3rd Party engineering firms and PA/ SCADA consultants assigned to plant IT pojects and deliverables. Responsibilities...
POSITION SUMMARY: Manage the design, implementation, and support for Plant-Wide Process Automation (PA) and Supervisory Control and Data Acquisition (SCADA) solutions within the Hamilton, OH facility used to support pharmaceutical development and manufacturing. Manage activites of 3rd Party engineering firms and PA/ SCADA consultants assigned to plant IT pojects and deliverables. Responsibilities...
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 ...
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 ...
Barry-Wehmiller Design Group Stewart, MN
Job Description: Design Group is a leading engineering, systems integration, and technology consulting firm, capable of providing complete operating solutions for consumer products, life sciences, and other industrial sectors. Design Group provides engineering, project management, regulatory compliance, and other technology services to the world’s leading companies. Our organization is staffed b...
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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