Automation Process Specialist
2 days ago
- Process and application owner for Automation and Manufacturing systems across site.
- Manage, plan & execute CI projects as well as provide required support as SME.
Support and Reliability
- Application owner for all Manufacturing systems and software packages.
- Responsible for Automation Architecture design and site standards for automation.
- Implement corrections, corrective actions, and countermeasures arising from CAPA's.
- Develop scope for capital projects targeted at both short and longer term needs.
- Act as user representative for capital projects or delivery agent for local projects.
- Understand equipment reliability issues with the objective of improvement.
- Provide technical expertise of equipment and processes in area of responsibility. This includes clear understanding of equipment flow chart/process flow document, critical process parameters, and master formula instructions for the process.
- Monitor/trend control systems as tool for verifying and optimizing equipment performance.
- Lead troubleshooting efforts to resolve more complex process and software problems.
- The Maintenance Tech/Electronics Tech is the first line of support in troubleshooting but will involve the Automation Process Specialist as needed.
- Utilize formal problem solving techniques, including Root Cause Analysis, FMEA to resolve equipment issues related to Automated systems.
- Respond to and initiate OEM requests related to complex Technical/software issues.
- Communicate effectively with others, especially process team members, customers, engineering, and production personnel, providing technical insight.
- Provide Application systems oversight to Electronics Tech(s) that support the area.
- Evaluate all activities for impact on qualified state of applications/servers where application changes or software changes are requested.
- Participate in Periodic Reviews for industrial network performance.
- Lead or participate in IQ/OQ/PQ and commissioning activities for software upgrades or implementation of new applications in the Virtual Environment.
- Coordinate with asset management personnel to align on improvements and assure alignment of useful lifecycle of hardware and related software to build risk register and submit Capex requests.
- Identify and drive improvement opportunities (procedural changes, upgrades, projects, etc.) associated with equipment within the area.
- Goals/objectives should target world-class levels of operation for safety, quality and customer service.
- Work with production supervisors and managers for optimal efficiency to meet the needs of internal and external customers.
- Communicate regarding schedule adjustments.
- Develop and manage project plans for software upgrades.
- Lead automation equipment lifecycle upgrade projects across site.
- Provide input to project User Requirements Specifications as per developed standards.
- Develop obsolescence plan for installed automation equipment.
- Assist CI team on OEE process improvements.
- Ensure change controls are actioned appropriately.
- Communicate automation and application risks to HOD and production departments.
- Lead risk assessments for IT related security patch updates or network outages related to manufacturing systems.
- Lead risk assessments for automation failures that have resulted in deviations or CAPA's.
- Review CPP and CQA's for critical manufacturing processes.
- Provide technical and operational input for manufacturing investigations.
- Provide technical reports and feedback as required for Automation/application related queries.
- Effectiveness reviews of CAPA's implemented.
Background/ Experience
- N6 or equivalent NQF level certificate (e.g. Electronic or Electrical Engineering) in Electronics or similar with 3 yrs experience in an Electronics Technician role OR High School diploma with 5+ yrs experience in an Electronics Technician Role within a pharmaceutical manufacturing facility.
- Siemens Accredited Training.
- Proficient in PLC programming, Networking and IT systems (Virtual Environments).
- Siemens Step7, Siemens TIA, Siemens WinCC, Versiondog, Wonderware system Platform, Metasys Building Management, Vshpere Virtual Environments, Pharmagraph.
- Electronics experience in a pharmaceutical sterile manufacturing environment.
- Computer literacy: proficiency in Excel, Word, Power point and ERP system.
- Complex pharmaceutical process experience.
- Problem solving techniques.
- Project management.
- Risk Assessment.
- Planning and Organising.
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