Engineer, Process Equipment and analytical support (JP12181)
Thousand Oaks, CA · Biotech/Pharmaceutical
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 send your resume to recruiting@3keyconsulting.com. If you 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 www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.