Senior CSV Lead — Pharma Validation & Compliance

APBA TG Human Resource Pte Ltd; Singapore; On-site; SGD 80,000 - 110,000; Full time

Job summary

A recruitment agency in Singapore is seeking an experienced professional for CSV management in pharmaceutical environments. The role involves leading validation activities, ensuring compliance with GxP regulations, and managing cross-functional stakeholder engagement. Ideal candidates will possess a Bachelor’s degree and over 10 years of relevant experience in CSV and GxP validation. Strong communication and leadership skills are essential for success in this position, which offers a dynamic working environment.

Qualifications

• 10+ years of experience in CSV, C&Q, and GxP system validation within pharmaceutical or biopharma manufacturing.
• Proven experience validating automation platforms.
• Strong understanding of GxP regulations, GAMP 5, SDLC, and data integrity.

Responsibilities

• Lead end-to-end CSV and C&Q lifecycle activities.
• Define CSV strategies and validation plans.
• Ensure compliance with FDA and global regulatory requirements.
• Act as the CSV SME during audits and inspections.

Skills

CSV management

Risk-based validation

Stakeholder management

Compliance with GxP regulations

Communication skills

Education

Bachelor’s degree in Engineering, Computer Science, Life Sciences, or related discipline

Tools

Kneat Gx

DeltaV

PLC

SCADA

BAS/HMI systems

Job description

A recruitment agency in Singapore is seeking an experienced professional for CSV management in pharmaceutical environments. The role involves leading validation activities, ensuring compliance with GxP regulations, and managing cross-functional stakeholder engagement. Ideal candidates will possess a Bachelor’s degree and over 10 years of relevant experience in CSV and GxP validation. Strong communication and leadership skills are essential for success in this position, which offers a dynamic working environment.