DeltaV Validation Engineer: GMP CSV Expert, Flexible Hours

No deviation Pte Ltd; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A pharmaceutical solutions company in Singapore is seeking an experienced Validation Engineer to support the validation lifecycle of automation systems in a regulated environment. The role includes creating documentation, executing protocols, and ensuring compliance with industry standards like cGMP. Candidates should have a degree in Engineering or Science, with at least 3 years of relevant experience, particularly in DeltaV coding and configuration. Join us to make a meaningful impact in the pharmaceutical industry!

Benefits

Generous Leave Policy

Comprehensive Health & Wellness Coverage

Professional Development Opportunities

Inclusive Culture

Qualifications

• Minimum 3 years of relevant CSV experience in a regulated environment.
• Hands-on commissioning experience with DeltaV and other automation systems.
• Proficient in Microsoft Office applications.

Responsibilities

• Develop and update validation documentation including protocols and reports.
• Generate and review CSV protocols for DeltaV processes.
• Support protocol execution and troubleshooting.

Skills

DeltaV coding

Configuration

Communication skills

Risk assessments

Regulatory compliance

Project management

Education

Degree in Engineering or Science disciplines

Tools

DeltaV

WinCC

Siemens

Rockwell

Job description

A pharmaceutical solutions company in Singapore is seeking an experienced Validation Engineer to support the validation lifecycle of automation systems in a regulated environment. The role includes creating documentation, executing protocols, and ensuring compliance with industry standards like cGMP. Candidates should have a degree in Engineering or Science, with at least 3 years of relevant experience, particularly in DeltaV coding and configuration. Join us to make a meaningful impact in the pharmaceutical industry!