GMP Validation Specialist — 1-Year Contract

GMP Technologies; Singapore; On-site; SGD 42,000 - 66,000; Full time

Job summary

GMP Technologies in Singapore seeks a Validation Officer (1 year contract) to support validation and QA activities ensuring GMP compliance for manufacturing processes, equipment, and systems.

The role involves drafting and reviewing validation docs, participating in audits and regulatory inspections, and assisting in CPV and NPI projects under supervision. A Bachelors in a relevant field is required, with 1–2 years of pharma validation experience.

Qualifications

• Bachelor's degree in analytical chemistry, chemical engineering, chemistry or pharmaceutical sciences or related discipline.
• 1–2 years in validation, QA, or manufacturing support in regulated environment.
• Knowledge of GMP and validation.
• Understanding of regulatory processes and audits.
• Ability to review protocols and reports.

Responsibilities

• Support validation activities for equipment, processes, cleaning, and systems.
• Assist in drafting, reviewing, maintaining validation docs, SOPs, reports.
• Support change control assessments for impact on validation and product quality.
• Review validation protocols and reports for GMP compliance.
• Participate in internal audits and regulatory inspections.
• Assist in deviation investigations and CPV documentation where applicable.
• Support validation activities for new projects and NPI under supervision.
• Assist periodic review of validated systems and CPV documentation.
• Coordinate documentation and data review for cleaning and method validation.
• Provide basic QA support for engineering deviations and GxP tracking.

Skills

Validation

Quality Assurance

Manufacturing support

GMP awareness

Audit readiness

Education

Bachelors in Chemistry/Pharma

Job description

GMP Technologies in Singapore seeks a Validation Officer (1 year contract) to support validation and QA activities ensuring GMP compliance for manufacturing processes, equipment, and systems.

The role involves drafting and reviewing validation docs, participating in audits and regulatory inspections, and assisting in CPV and NPI projects under supervision. A Bachelors in a relevant field is required, with 1–2 years of pharma validation experience.