Project Engineer

Anter Consulting Pte. Ltd; Singapore; On-site; SGD 75,000 - 95,000; Full time

Job summary

Anter Consulting Pte. Ltd in Singapore is looking for a skilled professional to lead commissioning, qualification, and validation (CQV) activities for various projects. The ideal candidate will manage project timelines, coordinate with cross-functional teams, and ensure compliance with GMP standards.

Applicants should have a Bachelor's degree in Engineering and 5-7 years of relevant experience in the pharmaceutical or biotech sector. This is a great opportunity to drive impactful projects within a dynamic team.

Qualifications

• Bachelor's degree in Engineering or a related field.
• 5-7 years of experience in CQV, validation, and commissioning, preferably in pharmaceutical or biotech.
• Strong understanding of GMP standards and regulatory compliance.
• Proven ability to manage multiple projects and priorities effectively.
• Excellent problem-solving and communication skills.

Responsibilities

• Lead and support commissioning, qualification, and validation activities for assigned projects.
• Manage project timelines, ensuring deliverables are met within scope, budget, and regulatory compliance.
• Develop and execute validation protocols for equipment and systems.
• Coordinate with cross-functional teams for seamless project execution.
• Identify and resolve technical issues during commissioning and qualification phases.
• Support continuous improvement initiatives to optimize processes.

Skills

CQV processes

GMP standards

Project management

Problem-solving

Communication skills

Education

Bachelor's degree in Engineering or related field

Job description

Roles & Responsibilities

• Lead and support commissioning, qualification, and validation (CQV) activities for assigned projects.
• Manage project timelines, ensuring deliverables are met within scope, budget, and regulatory compliance.
• Develop and execute validation protocols (FAT/SAT, IQ, OQ, PQ) for equipment and systems.
• Coordinate with cross-functional teams, including manufacturing, quality, and engineering, to ensure seamless project execution.
• Identify and resolve technical issues during commissioning and qualification phases.
• Support continuous improvement initiatives to optimize processes and enhance project outcomes.

Qualifications and Experience

• Bachelor's degree in Engineering or a related field.
• 5-7 years of experience in CQV, validation, and commissioning, preferably within the pharmaceutical or biotech industry.
• Strong understanding of GMP standards and regulatory compliance.
• Proven ability to manage multiple projects and priorities effectively.
• Excellent problem-solving and communication skills.