QA Oversight Validation Engineer- BioPharma

PROCESS ENGINEERING SPECIALISTS PTE. LTD.; Singapore; On-site; USD 50,000 - 80,000; Full time

Job summary

An established industry player is seeking a dedicated QA Validation Engineer to join their team. In this pivotal role, you will provide oversight of commissioning and validation activities, ensuring that facilities and systems meet compliance standards. Your expertise will be crucial in reviewing documentation, executing validation deliverables, and supporting operational readiness. This position offers a unique opportunity to work on diverse projects within the Life Sciences industry, contributing to high-quality outcomes for multinational clients. If you are passionate about quality assurance and thrive in a collaborative environment, this role is perfect for you.

Qualifications

• Experience in commissioning and validation activities in the Life Sciences sector.
• Strong understanding of compliance standards and GMP operations.

Responsibilities

• Oversee commissioning and validation activities to ensure compliance.
• Review and approve documentation to meet project requirements.

Skills

Commissioning Oversight

Validation Activities

Documentation Review

Risk Assessments

GMP Operations

Education

Bachelor's Degree in Engineering or related field

Certification in Quality Assurance

Job description

PES

is an international services company providing Project Management, Construction Management, Commissioning & Qualification, and Automation services to our clients in the pharmaceutical, nutritional, and related sectors.

With offices across Europe, Asia, and the US, our core focus is on consistently delivering high-quality outcomes for our multinational clients.

This focus, along with our people's experience in delivering consistent quality results over the past 20 years, has been key to our success.

We are currently looking for a QA Validation Engineer to join us on a permanent basis to help deliver various projects in the Life Sciences Industry.

Key Attributes/Responsibilities

• Provide overall oversight of commissioning and validation activities to ensure facilities, equipment, technology, and systems achieve validated status as per project requirements.
• Ensure timely execution of commissioning and validation deliverables in alignment with the approved Commissioning and Validation Plan and project schedule.
• Review and approve facility, equipment, and system commissioning and qualification documentation to meet compliance standards.
• Review and endorse data mapping exercises and risk assessments to support validation and operational readiness.
• Evaluate and approve engineering deliverables, including maintenance strategies, critical instrument assessments, and master data records.
• Review and approve operational procedures to ensure seamless and compliant facility startup and integration into GMP operations.

If you'd like to find out about this opportunity, please forward your CV to Nelson Anthony at [e-mail].

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PES International operates as an equal opportunity employer. No terminology in this advert is intended to discriminate on the grounds of age, race, religion, sexual orientation, or any other factors unrelated to employment skills. We welcome applications from persons of all backgrounds for this role.