Engineer Senior

Thousand Oaks, CA 91320

Posted: 06/10/2024 Job Number: 39292

Job Description


Engineer Senior


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

Red Flags:
  • No work experience
  • No engineering or technical experience
  • No collaboration experience
  • No work gap of more than 3 months

Summary:

This engineering position supports manufacturing activities associated with manufacturing equipment and facilities at Thousand Oaks (TO). 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.

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

Skills:
  • 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

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

Preferred Qualifications:
  • 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

 

Pay range is $38 - $43 per hour with full benefits available, including paid time off, medical/dental/vision/life insurance, 401K, parental leave, and more. Our compensation reflects the cost of labor across several US geographic markets. Pay is based on several factors including market location and may vary depending on job-related knowledge, skills, and experience.

THE PROMISES WE MAKE:

At Crystal Equation, we empower people and advance technology initiatives by building trust.  Your recruiter will prep you for the interview, obtain feedback, guide you through any necessary paperwork and provide everything you need for a successful start.  We will serve to empower you along the way and provide the path for your professional journey.

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About Thousand Oaks, CA

Ready to take your career to the next level in the vibrant city of Thousand Oaks, California? Nestled in the heart of Ventura County, this bustling city offers a perfect blend of suburban charm and urban amenities. With a strong job market, top-notch schools, and breathtaking views of the Santa Monica Mountains, Thousand Oaks is an ideal location for professionals seeking growth and fulfillment. Explore job opportunities near iconic sites like the Gardens of the World, catch a show at the Fred Kavli Theatre, or indulge in the local culinary scene featuring dishes from around the world. Join this dynamic community and unlock your potential in Thousand Oaks! Start your job search now to find your perfect fit in this captivating city.