Job Description:
Location: Thousand Oaks, CA
Salary: $40.00 USD Hourly - $50.00 USD Hourly
Description:
Description:
Candidates needs to have 4 - 6 years pharmaceutical industry background. Bachelor degree Engineering and manufacturing background.
This engineering position supports manufacturing activities associated with manufacturing equipment and facilities at Thousand Oaks (ATO). 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.
This engineering position supports manufacturing activities associated with manufacturing process equipment at Amgen Thousand Oaks (ATO). The engineer works in partnership with the maintenance, Project Management, Engineering Technical Lead, and manufacturing to develop, improve and oversee the operation and reliability of equipment. The Engineer role will provide direct engineering technical support as follows:
• Identify, support, and/or lead implementation of engineering based improvements or
upgrades to the equipment systems. This may include development of reason 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.
• 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.
• Be individually accountable for the verification deliverables on key capital projects.
• Advising and coordinating equipment maintenance as vital to ensure systems are in proper working order.
• Provide oversight for verification deliverables developed by outsourced/contract verification staff.
• Develop commissioning and function test plan for any equipment modifications and acquisition.
• Ensure safety during commissioning, validation, maintenance and manufacturing activities.
• Support Manufacturing and QA with Performance Qualification (PQ) activities if applicable.
• Act as a liaison between Engineering and Manufacturing during project planning,
execution, and closeout.
• Monitor systems to identify performance risks and implement risk reduction strategies.
• Providing problem solving support to reduce production downtime. This will involve leading and/or supporting technical root cause analysis involving multidisciplinary site teams and implementation of corrective/preventive action.
• Support new product/technology introductions by performing engineering assessments,
implementing equipment modifications and supporting engineering runs.
• Ensure systems are installed and operating safely align with pertinent environmental health/safety practice, rules and regulations.
• Provide ad hoc technical support and guidance for manufacturing and maintenance.
• Provide coaching and guidance to project teams and engineers on the CQP process and risk-based approaches to commissioning and verification.
• Assist in developing and maintaining metrics.
• Full time onsite support in required.
• Work schedule flexibility to support 24/7 operations, requiring occasional after-hours engineering coverage as required from time to time
Demonstrated skills in the following areas:
• 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/troubleshooting 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.
• Project Cost development
• Conflict Resolution
• Customer service in a technical setting
• Management of contractors and vendors.
• 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
Preferred Qualifications / Skills / Experience:
• Bachelor's degree in chemical or other Engineering fields
• 6+ years of relevant work experience with 5+ years' experience in Biopharmaceutical
operations/manufacturing environment
• Experience working in a regulated environment (e.g. cGMP, OSHA, EPA, etc.) and
familiarity with GMP quality systems/processes such as change control, deviations,
corrective and preventative actions, and qualifications/validation.
• Direct knowledge of design and troubleshooting with GMP Biopharmaceutical Production
facility equipment/systems such as cell culture reactors, chromatography, filtration, as well as other equipment needed to support these processes such as autoclaves, clean in place (CIP) systems, washers, clean steam, 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.)
• Experience applying engineering principles to the design and implementation of system modifications, introduction of new processes, and execution of capital projects
• Understanding of the execution process of capital projects in a GMP and/or non-GMP
Biopharmaceutical Production facility including procurement, construction, startup, and
validation
• Understanding of safety requirements working in a Biopharmaceutical Production facility.
• Independent, self-motivated, organized, able to multi-task in project environments, and
skilled in communication, facilitation, and collaboration
• Phenomenal teammate prepared to work in and adopt a team-based culture that relies on collaboration for effective decision-making
• Strong leadership, technical writing, and communication/presentation skills
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
Top 3 Must Have Skill Sets:
1. 4 to 6 years Engineering and technical background on process equipment in pharmaceutical industry
2. No work gap more than 3 months
3. Demonstrated to be motivated to take on new challenges
4. Demonstrated ability to solve complex problems by being detail oriented and data driven
5. Has shown cross functional collaboration with multidiscipline functions such as process development, engineering, automation, maintenance and management
Day to Day Responsibilities:
• Identify, support, and/or lead implementation of engineering-based improvements or
upgrades to the equipment systems. This may include development of reason 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.
• 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.
• Be individually accountable for the verification deliverables on key capital projects.
• Advising and coordinating equipment maintenance as vital to ensure systems are in proper working order.
• Provide oversight for verification deliverables developed by outsourced/contract verification staff.
• Develop commissioning and function test plan for any equipment modifications and acquisition.
• Ensure safety during commissioning, validation, maintenance and manufacturing activities.
• Support Manufacturing and QA with Performance Qualification (PQ) activities if applicable.
• Act as a liaison between Engineering and Manufacturing during project planning,
execution, and closeout.
• Monitor systems to identify performance risks and implement risk reduction strategies.
• Providing problem solving support to reduce production downtime. This will involve leading and/or supporting technical root cause analysis involving multidisciplinary site teams and implementation of corrective/preventive action.
• Support new product/technology introductions by performing engineering assessments,
implementing equipment modifications and supporting engineering runs.
• Ensure systems are installed and operating safely align with pertinent environmental health/safety practice, rules and regulations.
• Provide ad hoc technical support and guidance for manufacturing and maintenance.
• Provide coaching and guidance to project teams and engineers on the CQP process and risk-based approaches to commissioning and verification.
• Assist in developing and maintaining metrics.
• Full time onsite support in required.
• Work schedule flexibility to support 24/7 operations, requiring occasional after-hours engineering coverage as required from time to time
Contact: vsharma02@judge.com
This job and many more are available through The Judge Group. Find us on the web at www.judge.com
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