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Job Description
Structured overview of role & requirementsAbout This Role
Own operation and troubleshooting of manufacturing automation systems including DeltaV DCS, SCADA & PLCs, supporting reliability and audit investigations related to automation.
Manage regulatory compliance aspects of site automation systems including system security, validation support, and adherence to 21 CFR Part 11 and cGAMP guidelines.
Develop and implement site automation standards, author and review design documents, support qualification activities, and provide automation guidance and training to other functional groups.
Minimum Requirements
Bachelor's degree in Electronics or Instrumentation Engineering or equivalent.
8 to 12 years experience in process control and automation (PLC, SCADA, DCS) within pharmaceuticals, biotechnology, or life sciences.
Capability to read and interpret electrical control system diagrams and strong technical knowledge in field instrumentation and industrial communication networks.
Familiarity with FDA, ISO, EU, and ICH industry practices; experience with sequel servers and databases; Work Location: On Premise.
Ideal Candidate Profile
Experience in pharmaceutical or biotechnology automation environments with compliance focus.
Strong technical proficiency to author/review automation design documents, lead qualification and validation activities.
Demonstrated capability to train others and leverage AI tools for problem solving and productivity enhancement, with understanding of responsible AI practices.
