Apply for the Automation Engineer VPE role at WuXi Biologics.
We are looking for an experienced Automation Engineer to support VPE systems in a GMP‑regulated environment. The candidate will develop automation strategies, deploy new technology, and maintain existing automation infrastructure.
Essential Duties and Responsibilities
* Strong experience with vendor‑packaged automation equipment – PLC/SCADA platforms.
* Ownership and administration of equipment control systems in a GMP‑regulated manufacturing setting.
* Lead and support system improvements, development of detailed specifications, engineering documents, and SOPs.
* Lead technical root‑cause analysis, incident investigations, and troubleshooting related to electrical, instrumentation, and equipment control systems.
* Support new product or technology introductions by performing engineering assessments, implementing automation system configuration changes, and supporting engineering runs.
* Solving complex problems, lifecycle management, and operational excellence.
* Develop and manage change‑control requests per established SOPs and processes.
* Support a safe working environment by complying with all pertinent environmental health & safety practices, rules, and regulations.
* System owner responsibilities such as change control, maintenance, backup/restore, disaster recovery, and regulatory compliance.
* Perform all duties in accordance with GMP requirements, SOPs, and controlled documents.
* Flexibility to take on additional tasks at the discretion of the AIS Team Lead.
* Act as a role model for the Engineering function and the wider organization in adherence to WuXi corporate core values and the PROUD culture.
Experience
* Manufacturing automation experience in biopharmaceutical or API facilities.
* Experience in PLC programming and troubleshooting, SCADA systems, Profibus networking.
* OSIsoft PI Data Historian – Siemens PLCs / SCADA and HMIs is a strong advantage.
* Experience in change control, non‑conformance, corrective and preventative actions, and validation practices.
* Experience developing automation strategies for new product introduction and new technology deployment.
Knowledge
* Knowledge of GAMP software development lifecycle, ANSI/ISA‑S88 and S95 industry standards, and 21 CFR Part 11.
* Strong network architecture or engineering proficiencies including TCP/IP, routing, switching, network IDS/IPS, Active Directory, domain integration, and firewalls.
* Excellent control systems automation background focused on design, installation, programming, validation, and lifecycle maintenance of automated equipment.
* Ensure application of corporate blueprint and standards using business drivers to local business needs and project requirements.
Qualifications
* Bachelor’s in electrical engineering, computer science, chemical engineering, biotech engineering, or related life science engineering with 5+ years’ experience in an operations/manufacturing environment.
* Independent, self‑motivated, organized, capable of multi‑tasking in project environments, and skilled in communication and collaboration.
* Excellent communication, interpersonal and presentation skills.
* Collaborative and inclusive approach to work and colleagues.
* Excellent problem‑solving and troubleshooting skills.
* Flexible approach to work and positive attitude – a good fit within the team dynamic.
* Engage cross‑functionally with a site‑based team.
* Autonomous, self‑starter who uses initiative to drive actions forward.
* Demonstrate strong ethics in adhering to company procedures, policies, regulatory standards, and customer expectations.
Seniority Level
* Mid‑Senior level
Employment Type
* Full‑time
Job Function
* Pharmaceutical Manufacturing
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