Senior Engineer, Value Stream Recipe Owner

Primarily accountable for the implementation, life-cycle, and ownership of the Parenterals PCS/MES and PLC process recipes related to the Fill/ Finish Value Stream.

Responsibilities include:

- Adherence to the global strategy & scope by maintaining/delivering/implementing the required process control within the DCS, PCS, MES and PLC systems for both new and legacy systems.

- Alignment of the system with the Global Execution Systems (Automation Engineering) approach within Manufacturing Operations.

- Technical project ownership for all Execution Systems related project deliverables including oversight & review of contractors/integrators work during support projects.

- Ownership of the process recipe and configuration across the Parenterals MES, PCS, and/or PLC

systems for the Fill/ Finish Value Stream.

- Incident tracking, remediation and improvement associated with the Fill/ Finish Value Stream.

- Tests and evaluates production equipment and machinery to ensure reliability and efficiency.

- Adapts machine and equipment design to plant and production conditions.

This scope will also include aligning and coordinating the definition of the required hardware with the System Owner; including the development of the software, and system coordination with the required project schedule to enable Commissioning and Validation of the Process Systems. Further, to coordinate and troubleshoot interfaces with the Data Historian, Data Acquisition Systems, Building Management Systems, Central Alarm Management System, Manufacturing Control Network, and Enterprise applications.

The role will be responsible for implementing modifications related to the process improvements, changes, support, and maintenance of the Parenterals Control Systems.

Qualifications:
• Bachelors in Engineering or Computer Science
• 3+ years of experience within Automation Technologies in the pharmaceutical industry
• Experience in biopharmaceutical industry and Engineering/Automation projects preferred
• Strong communication skills with customers, design teams, contractors, and management
• Action oriented skills; ability to learn on the fly
• Good problem solving, technical learning, time management and prioritizing skills
• Functional knowledge of cGMPs and manufacturing operations in FDA regulated facility

Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.

Our Benefits

CSL employees that work at least 30 hours per week are eligible for benefits effective day 1. We are committed to the wellbeing of our employees and their loved ones. CSL offers resources and benefits, from health care to financial protection, so you can focus on doing work that matters. Our benefits are designed to support the needs of our employees at every stage of their life. Whether you are considering starting a family, need help paying for emergency back up care or summer camp, looking for mental health resources, planning for your financial future, or supporting your favorite charity with a matching contribution, CSL has many benefits to help achieve your goals.

Please take the time to review our benefits site to see what's available to you as a CSL employee.
About CSL Behring

CSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. Learn more about CSL Behring.

We want CSL to reflect the world around us

As a global organization with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL.

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