Junior Validation Engineer - On-Site QC Systems (LCMS/GCMS)

PSC Biotech® Corporation; Singapore; On-site; SGD 42,000 - 54,000; Full time

Job summary

PSC Biotech Corporation is seeking a motivated engineer to join our biotech consultancy team in Singapore. The role focuses on P&ID review during commissioning, change control, validation documentation, and IQ/OQ/SAT work, with on-site support at client sites.

Fresh graduates with strong technical foundations are welcome, and the position offers an entry into top pharmaceutical client environments. On-site presence and hands-on validation activities are key aspects of the role.

Qualifications

• Bachelor’s Degree in a related engineering discipline.
• Fresh graduates with strong technical foundations are welcome to apply.
• Review of P&IDs during commissioning phase is required

Responsibilities

• Review of P&IDs during commissioning phase.
• Generation of Change control and System Impact Assessment (Kneat).
• Provide SAT support.
• Validation document generation and protocol for equipment, including, but not limited to, process equipment and utility systems, both paper or using e-validation systems (Kneat).
• Execution of IQ and review/support for OQ.
• Closure of Change Control implementation tasks.
• Work independently with the project manager, vendors, and contractors.
• Provide Quality service adhering to SOP requirements.
• Be present on-site to provide full-time support.
• Computerized systems in particular to Agilent LCMS and GCMS.
• Temperature Mapping
• Cleanroom Qualification

Skills

P&ID review

Quality assurance

Validation documentation

On-site support

Independent work

Education

Bachelor’s degree in related engineering

Tools

Kneat

Agilent LCMS

GCMS

Job description

PSC Biotech Corporation is seeking a motivated engineer to join our biotech consultancy team in Singapore. The role focuses on P&ID review during commissioning, change control, validation documentation, and IQ/OQ/SAT work, with on-site support at client sites.

Fresh graduates with strong technical foundations are welcome, and the position offers an entry into top pharmaceutical client environments. On-site presence and hands-on validation activities are key aspects of the role.