Senior Validation Engineer - Biopharma CQV Expert

Esco Aster; Singapore; On-site; SGD 60,000 - 80,000; Full time

Benefits offered by this job

Learning and Development

Competitive Compensation

Overseas Travel Opportunities

Job summary

A leading contract research organization in Singapore is looking for a qualified professional to join its MSAT team. The role involves risk-based commissioning and validation of pharmaceutical equipment while following GxP standards. Ideal candidates will have a degree in Engineering or Science, along with 3-5 years in the pharmaceutical industry. Proficiency in technical writing and strong teamwork skills are essential. This position offers the opportunity to contribute significantly to the company's mission of transforming solutions in biosciences.

Qualifications

• Minimum of 3-5 years’ experience in pharmaceutical/biopharmaceutical manufacturing.
• Familiar with working in a GxP environment.
• Good knowledge of CQV approaches including Validation Lifecycle.

Responsibilities

• Perform risk-based commissioning, qualification and validation of equipment.
• Develop validation protocols that fulfill regulatory requirements.
• Coordinate with internal teams to achieve CQV objectives.

Skills

Analytical skills

Technical writing

Communication skills

Team collaboration

Education

Degree and/or Diploma in Engineering/Science

Tools

MS Office Suite

Job description

A leading contract research organization in Singapore is looking for a qualified professional to join its MSAT team. The role involves risk-based commissioning and validation of pharmaceutical equipment while following GxP standards. Ideal candidates will have a degree in Engineering or Science, along with 3-5 years in the pharmaceutical industry. Proficiency in technical writing and strong teamwork skills are essential. This position offers the opportunity to contribute significantly to the company's mission of transforming solutions in biosciences.