Engineer Senior Job Number: 351028 Category: Manufacturing Engineering Description: Job Title: Reliability Engineer Job Type: 12 months of contract Location: Thousand Oaks, CA ZIP Code: 91320 Pay Rate: up to $48/hr. Start Date: Right Away Keywords: #Engineer #SeniorEngineer Responsibilities: This engineering position supports manufacturing activities associated with cGMP equipment and facilities at Client Thousand Oaks (ATO). The senior engineer works in partnership with the automation, maintenance, project management, corporate engineering, and manufacturing to develop and oversee the operation and reliability of equipment while driving safety and quality compliance. The engineer will support the department and capital projects and provide data to support business cases and long term strategy. The Senior Engineer role will provide direct engineering technical support as follows: * Demonstrating role modeling of leadership behaviors and positive values to create a positive working environment. * Be individually accountable for manufacturing equipment reliability and deliverables on key capital projects to deliver business targets and deliverables * Assist in the identification of critical quality parameters and process attributes for new equipment or facility modifications. * Suggest design modifications to address risks and design in quality and safety. * Develop the commissioning strategy based on the URS and Quality Risk Assessment for Automation and Equipment Systems (QRAES) to validate equipment design while minimizing project cost and schedule impact (risk-based approach). * Oversee development of validation protocols in line with CQP, Automation Systems Delivery SOPs, and cGMP standards. * Recommend, evaluate, and manage performance of contract resources * Provide oversight for verification deliverables developed by outsourced/contract verification staff. * Act as a liaison between engineering and quality assurance during project planning, execution, and closeout * Ensure that work executed with safety compliant practices and documented in accordance with cGMP good documentation * Review and approve the commissioning reports, maintenance practices and parts, and drive productivity improvement Related Activities: * Participate or lead, when required, multidisciplinary site teams, e.g. cross functional team, root cause analysis lead. * Support Lean Transformation and Excellence in Operations process improvement by leading, supporting, and documenting improvement opportunities to reduce cost, improve safety/quality, or improve speed. * Provide ad hoc technical support and guidance for manufacturing and maintenance * Provide coaching and guidance to project teams and engineers using risk-based approaches * Defend the equipment-specific calibration, maintenance, & validation as required during regulatory inspections * Participate in internal audits and assess in conjunction with quality assurance * Assist in developing and maintaining business metric performance Basic Qualifications Doctorate degree OR Master"s degree & 3 years of engineering and/or manufacturing experience OR Bachelor"s degree & 5 years of engineering and/or manufacturing experience OR Associate"s degree & 10 years of engineering and/or manufacturing experience OR High school diploma / GED & 12 years of engineering and/or manufacturing experience Preferred Qualifications / Skills / Experience * Bachelor's degree in engineering or another science-related field * 7+ years of relevant work experience with 5+ years" experience in operations/manufacturing environment * Direct experience with regulated environments (FDA, OSHA, EPA, etc.) * Working knowledge and experience with cGMP procedures and engineering practices on pharmaceutical/biotech production processes, clean utilities, facilities, instruments, and equipment * Experience implementing risk-based verification on major GMP process equipment / automation projects, including validation protocol development and execution * Understanding and awareness of industry/regulatory trends for verification/validation * Experience with combination product / medical device quality systems verification * Strong process equipment knowledge - cell culture, fermentation, purification, filling, and packaging * Strong process automation knowledge - understanding of automation infrastructure, current technologies, and automation project execution / verification. o Knowledge of Delta V, Rockwell, and Plant Information Systems is a plus * Demonstrated strong communication and technical writing skills * Strengths in facilitation and collaboration / networking * Experience in developing SOPs and delivering training * Individual must be a team player prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making * Proven track record of applying process improvement methodologies to mature and improve business processes (e.g. PDCA, LEAN, Six Sigma, and fundamental understanding of statistics, etc.) If you are interested in this role, please apply via the apply now link provided. Our overriding goal is to provide quality staffing solutions that help people, organizations, and communities succeed. Belcan is a leading provider of qualified personnel to many of the world's most respected enterprises. We offer excellent opportunities for contract, temporary, temp-to-hire, and direct assignments. We are the employer of choice for thousands worldwide. For more information, please visit our website at Belcan.com EOE/F/M/D/V Location: Thousand Oaks , CA Minimum Experience (yrs): Required Education: Master (MA, MS...) Benefits: Return to search results Email this job to a friend (emailjobs.asp?jo_num=351028) If you have previously registered with us, pleaseLog in (memberlogin.asp) to apply for this position. *Logged in members may also add jobs to their job cart