Quality Control Validation Engineer

Coalesce Management Consulting; Singapore; On-site; SGD 67,000 - 100,000; Full time

Job summary

Coalesce Management Consulting is recruiting a Validation Engineer to support the Quality Control team in Singapore. The role focuses on driving QC equipment qualification and compliance activities across the QC labs, ensuring devices and processes meet health, safety and quality requirements.

You will prepare URS, IOQ, PQ, QR, investigate deviations, coordinate with stakeholders, and contribute to risk assessments while adhering to HSE guidelines.

Qualifications

• Minimum 4 years of lab experience in the pharmaceutical industry.

Responsibilities

• Drive and support equipment qualification as per pre-defined timeline
• Guide and resolve standard issues relating to current processes and systems and qualification and validation approach within and across various functions to ensure all health, safety, quality or training procedures meet requirements
• Review and collaborate with stakeholders on to identify possible solutions on deviations and/ or project discrepancies
• Drive QC equipment qualification with deep knowledge on this project which includes URS, ERES, HLRA, Vendor IOQ, In-House IOQ, PQ, QR etc drafting and execution
• Drive qualification investigations as and when required
• Project progressing according to plan and quality expectations
• Other duties or projects assigned by the manager
• Comply with all HSE guidelines
• Detect and report potential accident, risks and propose solutions
• Participate in HSE risk assessments

Skills

Lab experience

Quality control

Job description

We are looking for a Validation Engineer to support the Quality Control team. The candidate is expected to support and drive QC equipment qualification and compliance related activities of QC labs in areas of equipment.

Key Responsibilities:

• Drive and support equipment qualification as per pre-defined timeline
• Guide and resolve standard issues relating to current processes and systems and qualification and validation approach within and across various functions to ensure all health, safety, quality or training procedures meet requirements
• Review and collaborate with stakeholders on to identify possible solutions on deviations and/ or project discrepancies
• Drive QC equipment qualification with deep knowledge on this project which includes URS, ERES, HLRA, Vendor IOQ, In-House IOQ, PQ, QR etc drafting and execution
• Drive qualification investigations as and when required
• Project progressing according to plan and quality expectations
• Other duties or projects assigned by the manager
• Comply with all HSE guidelines
• Detect and report potential accident, risks and propose solutions
• Participate in HSE risk assessments

Requirements:

• Min. 4 years of experience within the lab environment in the pharmaceutical industry