Senior Reliability Engineer Senior, Pharma Equipment​/Facilities; JP

Position: Senior Reliability Engineer Senior, Pharma Equipment/Facilities (JP13179)
Job Title:Senior Reliability Engineer Senior, Pharma Equipment/Facilities (JP13179)
Location:Thousand Oaks, Ca. 100% onsite.
Business Unit:Facilities and Equipment Drug Substance Supply
Employment Type: Contract
Duration:1+ years with possible extensions or conversion to FTE
Rate
: $44 - $50/hr w2 with benefits
Posting Date:10/04/2024

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Key Consulting is hiring! We are recruiting an
Engineer Senior, Biotech Manufacturing and Process Equipment
for a consulting engagement with our direct client, a leading global biotechnology company.
Ideal Candidate:
Bachelor Engineering process mechanical degree and 5 years of process equipment experience

Job Description:
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

Top 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,s 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

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.

Why is the Position Open?
Supplement additional workload on team

Red Flags:
No prior process equipment experience

Interview Process:
Phone interview, Webex panel.

We invite qualified candidates to sendyour resume to 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  You are also welcome to sharethis opportunity with anyone you think might be interested in applying for this role.
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