Senior Quality Specialist

NUSANTARA PRIME CONSULTING PTE. LTD.; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A consulting firm in Singapore is seeking a professional to lead a small team in executing tasks at client sites in the GMP pharmaceutical industry. The ideal candidate will have at least 5 years of experience, a diploma in engineering or sciences, and familiarity with aseptic techniques. Responsibilities include client liaison, ensuring project timelines, and executing environmental monitoring for cleanrooms. This position has a contract duration of 6 months with travel required to Tuas.

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/behaviors.
• Experienced in performed environmental monitoring.

Responsibilities

• Lead a small team to execute tasks at the client site.
• Act as the point of contact with the client regarding project status.
• Ensure client timelines for various project stages are met.
• Execute baseline environmental monitoring for classified cleanrooms.
• Complete qualification documents during execution.
• Participate in variation investigations and deviations.
• Ensure compliance in project documentation and real-time recording.

Skills

Team leadership

Client liaison

Environmental monitoring

Aseptic techniques

Education

Diploma in Engineering/Sciences or relevant discipline

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 term 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