Job Title: Engineer, Process Equipment and analytical support (JP12181) Location: Thousand Oaks, CA. 91320 Business Unit: F&E Drug Substance Supply Employment Type: Contract Duration: Initial 3 months with possible extensions of conversion to FTE Rate : $38 - $42/hour W2 Posting Date: 01/24/2024 Notes: Only qualified candidates need apply. Fully onsite. 3 Key Consulting is recruiting an Engineer, Process Equipment and Analytical Support for a consulting engagement with our direct client, a leading global biotechnology company. Ideally would have 2 - 5 years pharmaceutical industry background. Bachelor degree Engineering and manufacturing background. Job Description: This engineering position supports manufacturing activities associated with manufacturing equipment and facilities. The engineer works in partnership with the maintenance, Project Management, Engineering Technical Lead, and manufacturing to develop and oversee the operation and reliability of equipment. Demonstrated skills in the following areas: Problem solving and applied engineering. Basic technical report writing and presentations. Verbal communication Personal Organization Dealing with and managing change Technical (Equipment Specific) Analytical Problem Solving Computer Literacy (Maximo, Track wise, E-Builder, PCS, BMS and QEMS) Specialized equipment/process expertise Ability to handle multiple projects at the same time. Schedule development, facilitation and collaboration Basic project management, project completion and follow-up Problem solving skills requiring the application of scientific and engineering theory and calculations and creative skills in the development of hypotheses and approach. Negotiation, persuasion and facilitation Collaboration Project Cost development Conflict Resolution Customer service in a technical setting Management of contractors and vendors. Flexibility to work off-hours and fully on-site Top Must Have Skill Sets: Engineering and technical background (process equipment, troubleshooting, data driven tech skills) Ideally would have 2 - 5 years pharmaceutical industry background. Bachelor degree Engineering Team work experience Pharmaceutical equipment management background Day to Day Responsibilities: Be individually accountable for the verification deliverables. Suggest design modifications to address risks and design in quality and safety. Oversee development of validation protocols function test deliverables in line with CQP, Automation Systems Delivery SOPs, and standards. Act as a liaison between Engineering and Manufacturing during project planning, execution, and closeout Ensure safety during commissioning, validation, maintenance and manufacturing activities Responsible for equipment troubleshooting in a timely manner. Identifying reliability improvements for assigned equipment to improve equipment uptime. Provide ad hoc technical support and guidance for manufacturing and maintenance Provide concise and clear documentation for actions taken on systems Red Flags: No work experience No engineering or technical experience No collaboration experience No work gap of more than 3 months Interview Process: WebEx interview with a panel of 1:-3 (potentially) We invite qualified candidates to sendyour resume to recruiting@3keyconsulting.com . Ifyou decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role. #J-18808-Ljbffr 3key Consulting, Inc.
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