QA Validation Engineer - Pharma/GMP

PROCESS ENGINEERING SPECIALISTS PTE. LTD.; Singapore; On-site; SGD 80,000 - 100,000; Full time

Job summary

An international services company in Singapore is seeking a QA Validation Engineer to join their Quality Systems team. The role involves overseeing validation activities related to Data Integrity, collaborating with Subject Matter Experts, and engaging in discrepancy investigations. Ideal candidates should have experience in validation documentation and a strong understanding of quality processes. This permanent role presents an opportunity to contribute directly to critical projects in the Life Sciences industry.

Qualifications

• Experience in overseeing validation activities.
• Ability to conduct gap analyses and risk assessments.
• Familiarity with validation documents and protocols.

Responsibilities

• Oversee validation activities related to Data Integrity issues.
• Collaborate with Subject Matter Experts for validations.
• Engage in investigations of validation discrepancies.

Skills

Data Integrity

Validation activities

Risk assessments

SOP review

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 US, our core focus is on consistently delivering high-quality outcomes for our multinational clients.

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

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

Key Attributes/Responsibilities

• Contribute to the Quality Systems team by overseeing validation activities, particularly related to Data Integrity issues.
• Collaborate with the Subject Matter Expert to assist the validation team in conducting gap analyses and risk assessments before qualification activities, and suggest mitigation plans for identified gaps.
• Engage in investigations of validation discrepancies, help review and approve discrepancy reports, and support the closure of related CAPA actions.
• Review and approve validation documents, including protocols and reports.
• Provide assistance with any validation-related queries and issues.
• Review and approve standard operating procedures (SOPs), complete CQV lifecycle documentation

We are currently looking for candidates in Singapore.

If you'd like to find out about this opportunity or any other opportunity, please forward your CV to Sruthi Srikanth ([e-mail]).

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