Automation Engineer III
Oxford Biomedica
full-time
Posted on:
Location Type: Office
Location: Durham • North Carolina • United States
Visit company websiteExplore more
About the role
- Planning, execution, and monitoring of Automation systems utilized on site for cGMP manufacturing and facility utilities
- Provide technical support for automation projects, including automation system design, control system hardware, equipment design, control panel design, alarm management, and instrumentation start-up and troubleshooting
- Support development of technical standards, guidelines, and procedures in accordance with industry best practices
- Support automation system design and integration, including hardware/software design specification development, user / functional requirement development, integration, and validation in conjunction with IT Computer Systems Validation & QA Validation leads
- Develop P&IDs and loop descriptions for various processes, and/or equipment
- Partner with automation system service providers, contract resources and Instrument/Electrical technicians ensuring safe, compliant maintenance and project execution
- Maintain current contacts as needed for system support
- Support automation issue identification, communication, and resolution, including all compliance aspects such as Deviation investigation, Change Control, Corrective and Preventative Action (CAPA)
- Provide technical support for troubleshooting, improving, or optimizing ongoing manufacturing operations, including being on-call for after-hours remote support
- Support the design, configuration, administration and maintenance activities of the sites manufacturing computer and automation systems, including process control systems, building automation systems, manufacturing execution systems, and data historians
- Ability to evaluate automation systems from a compliance perspective and ensure adherence to applicable standards (i.e. 21CFR Part 11, EU Annex 11)
- Troubleshooting experience, both hardware and software, at a manufacturing cGMP operation with flexibility to support operations on off hours
Requirements
- Requires a BS/MS in Engineering or related field
- Must have 5+ years of experience working in a biotechnology company, with focus on cross functional support for cGMP manufacturing
- 5+ years of experience in the execution of the automation discipline in a regulated manufacturing environment
- Strong understanding of GMPs and good engineering practice (GEP), including ISA S88, GAMP, ASTM E2500, ISPE guidance, etc.
- Experience with HMI/SCADA packages such as: Rockwell RSView, FactoryTalk
- Experience with OSI PI
- Experience with PLCs such as: Rockwell, Siemens
- Experience owning SOPs, deviations, change controls, and CAPAs to support operations
- Experience in plant start up, equipment commissioning, and qualification is a plus
- Experience with recipe design and qualification for bioreactors or chromatography skids is a plus
Benefits
- Competitive total reward packages
- Wellbeing programs that support your mental and physical health
- Career development opportunities to help you grow and thrive
- Supportive, inclusive, and collaborative culture
- State-of-the-art labs and manufacturing facilities
- A company that lives its values: Responsible, Responsive, Resilient, Respect
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
automation system designcontrol system hardwareequipment designcontrol panel designalarm managementinstrumentation troubleshootingP&IDs developmentloop descriptionstroubleshootingrecipe design
Soft Skills
technical supportcross functional supportcommunicationproblem solvingflexibility
Certifications
BS in EngineeringMS in Engineering