overseeing reliability program for all the equipment
data analysis - looking at process trends, improvement projects
ensure improvement reliability on the equipment
data analysis
problem solving techniques
strong communication skills to work with team and implement projects
ideally pharma/med device
aerospace is fine if they have strong reliability bg
Day to Day:
monthly equipment review meetings
meet with 8 engineers to go over metric review for that equipment
weekly meetings on current issues
responsible for driving meeting
analyze the root cause
working with engineers to come up with solutions to address the issue
Thousand Oaks, CA
1 year contract
(Target PR: 45-46/hr)
100% Onsite Thousand oaks
Basic Qualifications
Doctorate degree OR Master degree and 3 years of experience OR Bachelor degree and 5 years of experience OR Associate degree and 10 years of experience OR High school diploma / GED and 12 years of experience
Why is the Position Open?
Supplement additional workload on team
Top 3 Must Have Skill Sets: • Experience working in a regulated environment (e.g. cGMP, OSHA, EPA, etc.) and familiarity with GMP quality systems/processes such as change control, non-conformances, corrective and preventative actions, and qualifications/validation • Direct knowledge of design and troubles hooting with GMP Biopharmaceutical Production facility equipment/systems such as cell culture reactors, chromatography, filtration, filling, lyophilization, inspection, device assembly, as well as other equipment needed to support these processes such as autoclaves, clean in place (CIP) systems, washers, clean steam, water for injection, etc. • Ability to analyze problems, develop and propose engineering solutions in a scientific manner using data-driven techniques and analyses (e.g., Root Cause Analysis (RCA), Statistical Process Control (SPC), Six Sigma, Predictive Maintenance, etc.)
Day to Day Responsibilities: • Identify, support, and/or lead implementation of engineering based improvements or upgrades to the equipment or facility systems. This may include development of business case for improvement and identification of design requirements and then translation of requirements into process equipment/system design, specification and supporting the construction, startup, and validation of equipment. • Directing and coordinating equipment maintenance as necessary to ensure systems are in proper working order • Monitor systems to identify performance risks and implement risk reduction strategies • Providing trouble shooting support to reduce production downtime. This will involve leading and/or supporting technical root cause analysis and implementation of corrective/preventive action
Employee Value Proposition:
Possible Extension:
Yes
Red Flags:
No prior process equipment experience
Interview Process:
Phone interview, available as soon as possible
Senior Reliability Engineer
Bachelor Engineering process mechanical degree and 5 years of experience
This engineering position supports manufacturing activities associated with cGMP equipment and facilities. The senior engineer works in partnership with the automation, maintenance, and manufacturing teams to develop and oversee the reliability of equipment while driving safety and quality compliance. The engineer will 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 accountable for manufacturing equipment reliability • Suggest design modifications to address risks and design in quality and safety. • Ensure that work executed with safety compliant practices and documented in accordance with cGMP good documentation