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Senior Automation Engineer (PLC/DCS)

Wuxi Biologics Biopharmaceuticals Singapore Private Limited

Singapore

On-site

SGD 80,000 - 100,000

Full time

Yesterday
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Job summary

A biopharmaceutical company in Singapore is seeking a qualified professional to take a lead role in design integration for automation systems. This position requires a degree in Chemical Engineering or related field and a minimum of 10 years of experience in the pharmaceutical or biologics industry. Candidates should have hands-on experience with biologics drug manufacturing processes and strong proficiency in major PLC brands. The role involves leading design activities, supporting audit processes, and initiating continuous improvement initiatives.

Qualifications

  • Minimum 10 years of relevant experience in the pharmaceutical or biologics industry.
  • Hands-on experience with biologics drug manufacturing processes.
  • Solid knowledge of DCS systems and practical experience in a major DCS platform.

Responsibilities

  • Act as key interface between GAIS technical team and design firms.
  • Support new facility design and validation for AIS systems.
  • Lead activities such as drafting design and commissioning documents.

Skills

Collaboration
Coordination
Interpersonal skills
Hands-on experience with biologics drug manufacturing
Proficiency with PLCs
Knowledge of GMP regulations

Education

Degree in Chemical Engineering
Degree in General Engineering
Degree in Biochemistry
Degree in Automation
Degree in Electrical & Instrumentation

Tools

DeltaV DCS
Job description
Responsibilities
  • Act as key interface between Global Automation & Integrated Services (GAIS) technical team and design firms on design actions and technical standards
  • Support new facility design and validation for AIS systems (DCS, PLC Systems).
  • Lead activities such as URS review to ensure all design consideration and technical requirement for integration are incorporated into the design.
  • Lead activities such as drafting and/or review design and commissioning documents (FS、FAT/SAT、IQ/OQ protocols etc) to ensure requirements are in place and validated.
  • Involve & in key system FATs and ensure the integration design and successfully tested.
  • Lead & coordinate the AIS discipline activities on site installation, commissioning and qualifications as per project plan and timeline. This includes management of System Integrators (SIs) and other system suppliers.
  • Lead/explore initiatives on new technology applications to projects to boost productivity and compliance.
  • Act Acts as project lead leading a team post project to support routine manufacturing activities for both clinical and commercial Drug Substance (DS) & Drug Product (DP) processes with focus on performance improvement for AIS systems.
  • Act as SME to support external and internal audits and follow up audit actions related to AIS discipline.
  • Initiate continuous improvement activities and implementing change control process to continuously improve the process and meet the customer and regulatory requirements.
  • Leading/Supporting other overseas AIS projects as needed for WuXi Biologics.
Requirements
  • Degree in Chemical Engineering, General Engineering, Biochemistry, Automation, or Electrical & Instrumentation.
  • Min 10 years of relevant experiences in the pharmaceutical or biologics industry.
  • Hands‑on experience with biologics drug manufacturing processes and familiarity with key VPE equipment in drug substance or drug product facilities.
  • Proficiency with at least one major PLC brand and strong understanding of integration strategies, including deployment experience aligned with GAMP5 validation principles.
  • Solid knowledge of DCS systems and concepts, with practical experience in at least one major DCS platform (e.g., DeltaV).
  • Strong collaboration, coordination, and interpersonal skills to work effectively across departments and with multi-disciplinary teams.
  • Ability to support overseas projects and adapt to different cultures and working practices.
  • Good understanding of GMP regulations and compliance requirements.
  • Effective communication skills to collaborate across regions and time zones.
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