QA Validation Engineer

COALESCE MANAGEMENT CONSULTING PTE. LIMITED; Singapore; On-site; SGD 70,000 - 90,000; Full time

Job summary

A management consulting firm in Singapore is seeking a QA Validation Engineer to ensure compliance with industry standards in the Life Science sector. The ideal candidate will have a degree in Science or Engineering and at least 5 years of experience, with strong interpersonal skills. This role offers exposure to major pharmaceutical companies and includes health coverage and training benefits.

Benefits

Annual leave benefits

Full health coverage

Training and development allowance

Qualifications

• At least 5 years of experience in manufacturing and biopharmaceutical industries.
• Exhibit continuous improvement mindset and innovative thinking.

Responsibilities

• Review manufacturing batch records and production logbooks.
• Ensure compliance with FDA regulations on pharmaceutical projects.
• Conduct internal audits and review technical documentation.

Skills

Good knowledge of GMP facilities

Strong interpersonal and communication skills

Ability to multitask in a fast-paced environment

Education

Degree related to Science or Engineering

Job description

Overview

We are Coalesce Management Consulting - a community of people with a strong passion for excellence. We deliver bespoke project solutions within the Life Science and Technology sectors through our community of high-calibre industry specialists.

We are currently expanding our team and are looking for a QA Validation Engineer to support projects on-site with a client.

Responsibilities

• Reviewing manufacturing batch records, lot disposition, and production logbooks
• Ensure that all pharmaceutical projects comply with relevant industry standards, including FDA regulations.
• Reviewing and approving of vendor protocols, validation protocols, configuration specifications, requirement specification, requirement traceability matrix, summary report for Qualification
• Reviewing and approving CIP and SIP qualification and requalification documents, cleaning verification and validation documents
• Oversee non-conformance handling and equipment calibration
• Conduct internal audits and review technical documentation

Requirements

• Degree related to Science or Engineering.
• Good knowledge and experience in GMP facilities.
• At least 5 years of experience in manufacturing, and biopharmaceutical industries.
• Ability to multitask and work in a fast-paced environment with competing priorities.
• Strong interpersonal and communication skills and ability to develop close working relationships and work collaboratively with internal and external contacts at all levels.
• Exhibit continuous improvement mindset and innovative thinking

What’s in it for you?

• Greatest exposure to the Big Pharmaceutical Companies in the industry.
• Annual leave benefits.
• Full Health coverage and benefits.
• Training and Development allowance.

If you are interested in applying for this position, please send an email to [e-mail].

Coalesce Management Consulting 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 with no bearing to employment skills and we confirm that we are happy to accept applications from persons of any background for this role.