Validation Officer (1 year contract) | Pharma MNC | West

GMP Technologies; Singapore; Vor Ort; SGD 42.000 - 66.000; Vollzeit

Zusammenfassung

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.

Qualifikationen

• 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.

Aufgaben

• 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.

Kenntnisse

Validation

Quality Assurance

Manufacturing support

GMP awareness

Audit readiness

Ausbildung

Bachelors in Chemistry/Pharma

Jobbeschreibung

Validation Officer (1 year contract) | Pharma MNC | West

Job Openings Validation Officer (1 year contract) | Pharma MNC | West

About the job Validation Officer (1 year contract) | Pharma MNC | West

Purpose: Support validation and quality activities to ensure manufacturing processes, equipment, and systems comply with GMP and regulatory requirements, under guidance from senior validation or QA staff.

Jobscope:

• Support validation activities for equipment, processes, cleaning, and systems in accordance with approved protocols and procedures.
• Assist in drafting, reviewing, and maintaining validation documentation, SOPs, and reports.
• Support change control assessments to identify potential impact on validation and product quality.
• Review validation protocols and reports for completeness and GMP compliance.
• Participate in internal audits and regulatory inspections as a supporting team member.
• Assist in deviation investigations, including documentation review and impact assessment on validation status.
• Support validation activities for new projects and New Product Introduction (NPI) under supervision.
• Assist in periodic review of validated systems and support Continued Process Verification (CPV) documentation.
• Support cleaning and method validation activities by coordinating documentation and data review.
• Provide basic QA support for engineering activities such as preventive maintenance deviations and GxP documentation tracking.

Requirements:

• Min. Bachelors Degree in Analytical chemistry, chemical engineering, chemistry, pharmaceutical sciences or related discipline
• Min. 1-2 years of experience in validation, QA, or manufacturing support within a pharmaceutical, biotech, or regulated manufacturing environment
• Good knowledge of GMP and validation
• Good knowledge of quality and manufacturing process knowledge
• Basic knowledge of corporate management systems
• Good knowledge of re gulatory processes and audit

We regret that only shortlisted candidates will be notified.