Job Detail

About CSL

With operations in 35+ nations and ~27,000 employees worldwide, CSL is driven to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment.

CSL is the parent company of CSL Behring and Seqirus. CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions. CSL Behring operates CSL Plasma, one of the world's largest collectors of human plasma, which is used to create CSL’s therapies. Seqirus is one of the largest influenza vaccine companies in the world and is a transcontinental partner in pandemic preparedness and a major contributor to the prevention and control of influenza globally.

We invite you to take a look at the many career possibilities available around the globe and consider building your promising future at CSL by becoming a member of our team!

Stellenbeschreibung

CSL Behring is a global biotherapeutics leader driven by its promise to save lives. In Bern more than 1500 employees develop and deliver life-saving therapies to treat people with rare and serious medical conditions worldwide.

We are currently looking for an experienced

Senior Value Stream Recipe Owner - Engineer

As a successful Senior Value Stream Recipe Owner you are primarily accountable for the implementation, maintenance and ownership of the PCS/MES and PLC process recipes related to the specific 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. 


• Technical project subject matter expert for Execution Systems related project deliverables including oversight & review of contractors/integrators work


• 24/7 and/or on-call Manufacturing support of the facilities with the goal of maximizing facility uptime.


• Incident tracking, remediation and improvement associated with the assigned Value Stream


• Aligning and coordinating the definition of the required hardware with the Platform Owner; including the development of the software, and system coordination with the required project schedule to enable Commissioning and Validation of the Process Systems to meet the overall project schedule aligned to GAMP 5


• Coordination of interfaces with the Data Historian, Data Acquisition Systems, Building Management Systems, Central Alarm Management System, Manufacturing Control Network, and Enterprise applications.

• Work closely together with the work package owner of Library and Standards to ensure the defined standards are followed consistently throughout the project and the library modules are used as intended.

• Installation and configuration to the ISA-S88/S95 standard following Project phases: Requirements definition, detailed design generation, software configuration, system integration and Qualification testing.


• Participates in the creation of the Execution System validation strategy together with the Global and Site CSV & Quality representatives and ensure strong contribution to audit inspection.


• Responsible for ES investigations and CAPAs.


• Develop validation test cases and perform testing

Who you are:

• Bachelor of Science in an Engineering or other Science discipline/Masters preferred, Computer Science, or Management Information Systems.


• 5 years' practical experience in pharmaceutical industry including direct management experience in Manufacturing, Engineering or Execution Systems/Automation; 5 years or more working experience in Execution Systems/Automation design and support


• Specific experience in process automation, MES and batch manufacturing industry standards (ISA S88 &S95).


• Hands on experience in Recipe and Workflow Authoring (e.g.: Base Fractionation, Mfg., Packaging) and on experience in configuring master data and equipment in MES.


• Direct experience designing, building, deploying and supporting automation and execution systems in a regulated large-scale process-based manufacturing environment.


• Experience in running site-based shop floor systems in a globally distributed footprint is highly desirable.


• Experience in Process Excellence methodology is desirable, but not required.


• Must have demonstrated capability for technical leading of complex DCS/PCS /Automation projects with integrated MES systems initial development through validation of the facility


• Competencies: proven leadership, customer orientation, results and value orientation, collaboration and influencing, change management, interpersonal savvy, strategic/innovation