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Process Engineer I/II

CSL
USA
Full-time
Junior · 1+ years experience
Onsite
Discovered 1 weeks ago
Workday

Full Job Posting

About CSL Seqirus

CSL Seqirus is part of CSL. As one of the largest influenza vaccine providers in the world, CSL Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. With state-of-the-art production facilities in the U.S., the U.K. and Australia, CSL Seqirus utilizes egg, cell and adjuvant technologies to offer a broad portfolio of differentiated influenza vaccines in more than 20 countries around the world.

To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/.

Our Benefits

For more information on CSL benefits visit How CSL Supports Your Well-being | CSL.

You Belong at CSL

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.

To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging

Equal Opportunity Employer

CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement.

Watch our ‘On the Front Line’ video to learn more about CSL Seqirus

Qualifications

  • Education Bachelor’s degree in Engineering or related technical field.
  • Bachelor’s degree with 1+ years (Eng I) or 3+ years (Eng II) related industry experience, or Master’s degree with 1+ year's experience.
  • Occupational Standards
  • Bending/Reaching
  • For equipment operation or material movement tasks Computer Use
  • May be for greater than 4 hours per day Noise
  • Environment may exceed 80 decibels
  • Walking/Standing
  • Up to 8 hours throughout the workday
  • Lifting
  • Up to 40 lb.
  • Experience

Preferred Qualifications

  • Experience in pharmaceutical/biotech operations or other regulated environments (e.g., cGMP, OSHA, EPA) is preferred.
  • Experience with cell culture/fermentation and/or protein purification processes is preferred.

Responsibilities

  • The Process Engineer I / II will provide engineering support for Bulk Drug Substance Manufacturing operations. This includes process equipment troubleshooting as well as assisting in the design, procurement, installation, and start-up of process equipment systems.
  • Major Responsibilities
  • Provides technical review of design documents for assigned systems
  • Performs engineering tasks for the design, procurement, fabrication, and/or commissioning phases associated with standard or custom systems
  • Independently leads small engineering projects and change controls including concept, funding requests, and approvals
  • Independently performs start-up and commissioning activities on assigned systems
  • Troubleshoots complex equipment and/or automation related issues and develops sound engineering solutions to address identified problems for assigned systems
  • Recommends and implements performance and reliability improvements for assigned systems
  • Leads complex deviation (DR) investigations to adequately identify root cause and implement appropriate corrective and preventive actions (CAPAs).
  • Collaborates within the Process Engineering team as well as with other functions to accomplish continuous improvement projects and initiatives.

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