Senior CQV & Validation Engineer

ESCO ASTER PTE. LTD.; Singapore; On-site; SGD 55,000 - 75,000; Full time

Job summary

A prominent life sciences organization in Singapore is seeking to hire a team member for the MSAT group. The role focuses on ensuring commissioning, qualification, and validation activities align with GxP standards, contributing to continuous improvement in a collaborative team environment. Candidates should possess a relevant degree and 1-3 years’ experience in the biopharmaceutical sector, with strong communication and technical writing skills. The position offers opportunities for growth and international project involvement.

Qualifications

• Minimum of 1-3 years’ experience in pharmaceutical/biopharmaceutical manufacturing.
• Familiar with GxP environment and current regulations.
• Able to work independently and self-motivated.

Responsibilities

• Perform risk-based commissioning, qualification and validation of equipment and processes.
• Develop validation protocols and reports.
• Coordinate with internal teams to achieve CQV objectives.

Skills

Technical writing

Communication skills

Teamwork

GxP knowledge

Proficiency in MS Office Suite

Education

Degree or Diploma in Engineering/Science

Job description

A prominent life sciences organization in Singapore is seeking to hire a team member for the MSAT group. The role focuses on ensuring commissioning, qualification, and validation activities align with GxP standards, contributing to continuous improvement in a collaborative team environment. Candidates should possess a relevant degree and 1-3 years’ experience in the biopharmaceutical sector, with strong communication and technical writing skills. The position offers opportunities for growth and international project involvement.