Senior CSV Engineer (Pharma/Biotech)

NUSANTARA PRIME CONSULTING PTE. LTD.; Singapore; On-site; SGD 60,000 - 90,000; Part time

Job summary

A leading consulting firm in Singapore is seeking a senior-level professional to lead CSV activities for Computer Systems including DeltaV, PLCs, and MES. The ideal candidate will have substantial experience in biotech validation, strong analytical skills, and the ability to manage the Computer System Validation Lifecycle from design to execution. This role requires autonomy, excellent communication, and teamwork abilities. Duration is 9 months with the option to extend based on performance review.

Qualifications

• Bachelor of Science/Engineering or higher in a scientific or engineering discipline.
• Proven senior-level experience in biotech validation work.
• Track record of independently planning, executing, and closing CSV activities.

Responsibilities

• Lead CSV activities for Computer Systems e.g. DeltaV, BAS, PLCs, MES.
• Manage Computer System Validation Lifecycle from design to execution phases.
• Responsible for preparation of CSV documents and protocols.

Skills

Biotech validation

Test case execution

Process documentation

Cross-functional collaboration

Analytical skills

Education

Bachelor of Science/Engineering

Tools

ValGenesis software

Job description

Responsibilities

• Lead CSV activities for Computer Systems e.g. DeltaV, BAS, PLCs, MES and related mini-projects.
• Manage Computer System Validation Lifecycle from design to execution phases, including relevant CSV documentations such as Configuration specification, design review, commissioning documents, and protocols.
• Responsible for preparation of CSV documents and protocols, perform execution for automated equipment and/or control systems, and closure of executed protocols.
• Work largely requires use of valgenesis software to create validation documents and electronic test case execution.
• Work with SME to generate test cases and CSV documents.
• Provide guidance on test case execution and exception handling.
• Support SME on documentation matters and ensure documents are completed in time.
• Any other task as assigned by Supervisor/Manager.

About You

• Bachelor of Science/Engineering or higher in a scientific or engineering discipline
• Proven senior‑level experience in biotech validation work
• A track record of independently planning, executing, and closing CSV activities
• Able to work independently with not much supervision
• Strong autonomy in generating lifecycle documentations, test plan/cases, managing exceptions, and completing deliverables.
• Demonstrated proficiency of written and verbal communication skills with ability to communicate and collaborate effectively with cross‑functional teams
• Must be team player, curious with strong analytical and organizational skills
• Strong ownership

Duration: 9 months. Option to extend/convert subject to performance review.