Senior Quality Specialist

Nusantara Prime Consulting Pte. Ltd.; Singapore; On-site; SGD 80,000 - 100,000; Full time

Job summary

A consulting firm in Singapore is looking for a professional to lead project execution at client sites. The role requires at least 5 years of experience in the GMP pharmaceutical industry, with a focus on cleanroom operations. Candidates will manage timelines, liaise with clients, and ensure compliance with quality standards during project execution. This position will last for 6 months and includes responsibilities for environmental monitoring and documentation. Willingness to travel to Tuas is necessary.

Qualifications

• Minimum Diploma in Engineering/Sciences or relevant discipline.
• At least 5 years of relevant working experience in GMP pharmaceutical industry with cleanroom experience.
• Familiar with aseptic techniques and behaviors.

Responsibilities

• Lead a small team to execute tasks at the client site.
• Point of contact with the client regarding project status.
• Ensure timeline adherence for various stages of the project.

Skills

GMP pharmaceutical experience

Environmental monitoring

Aseptic techniques

Education

Diploma in Engineering/Sciences

Job description

Responsibilities

• Lead a small team to execute and carry out the tasks at the client site.
• Will be the point of contact with the client, liaising in terms of the project status and etc.
• Ensure that timeline from client on the various stages of the project are met.
• Execute baseline environmental monitoring, and EMPQ for classified cleanrooms (Grade C/D), and clean air devices (Grade A/B/C/D) for manufacturing lines.
• Complete qualification documents during execution of qualification.
• Participate in variation investigation and/or deviations.
• Compliance in project documentation based on required quality level e.g. (but not limited to), completing the record during execution in real time, correction of documentation errors.

Requirements

• Minimum Diploma in Engineering/Sciences or relevant discipline.
• At least 5 years of relevant working experience in GMP pharmaceutical industry with cleanroom experience.
• Familiar with aseptic techniques/behaviors.
• Experienced in performed environmental monitoring.
• Willing to travel to Tuas.

Contract Duration: 6 months