Sr. Automation Engineer - ReqCode 12-9840
Teva Pharmaceuticals - Irvine, CAThis job is no longer active. View similar jobs
- Teva Pharmaceuticals Teva Pharmaceuticals
- Irvine, CA
- Job Type
- Job Classification
- Full Time
- Mid-Career (2 - 15 years)
- High School Diploma or GED
- Company Ref #
- AJE Ref #
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Teva Parenteral Medicines is a global leader in the manufacture of generic injectable pharmaceuticals. A member of TEVA Pharmaceuticals Industries, the world's leading manufacturer and marketer of generic drugs. The company's mission is to play a leading role in the transformation of the U.S. healthcare system through its preeminence in the development, manufacture and marketing of generic pharmaceuticals. Teva Parenteral Medicines has an excellent opportunity for Sr. Automation Engineer.
The Sr. Automation Engineer can directly impact the acceptability of finished product; therefore, a high level of independent technical ability is required of this individual. This individual plans and executes automation/controls projects from concept to final closeout in support of site objectives. This position assumes responsibility as the technical owner of various automation and manufacturing systems and applies available resources to manage them.
Engineer and manage medium to large process control system/equipment improvement, optimization, expansion and upgrade projects to meet site objectives. Engineer and manage new process control/automation projects from the concept to commissioning and validation
Provide moderate to advance technical assistance to site operating groups through investigations, control system assessments, and design support.
Assist in preparation and execution of the Validation Qualification protocols related to automated and control systems. Provides technical and non-technical feedback to validation personnel for the successful qualification of systems.
Help to troubleshoot and diagnose Control system complex problems, working closely with Control System/Instrumentation Technicians and maintenance personnel
Update and develop User Requirement Specifications, Functional Specifications, Design Specifications, Operation and Maintenance Manuals for the new and existing control systems
Work closely with IT groups as a cross functional team member to meet automation project objectives.
Apply GMP principles within the workplace. Incorporate cGMP and regulatory compliance into all assigned project scopes, design and construction activities.
The position will require 5-10% travel for equipment FATs, system evaluations, and/or conferences or technical training
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