Scientist

NUSANTARA PRIME CONSULTING PTE. LTD.; Singapore; On-site; SGD 50,000 - 70,000; Full time

Job summary

A leading consulting firm in Singapore is seeking a Quality Control Specialist to manage test samples, ensure compliance with cGMP, and oversee QC instruments and electronic systems like LIMS and EMPOWER. The ideal candidate holds a Bachelor’s degree in a scientific field and has a strong quality mindset. Strong interpersonal and communication skills are essential as you will collaborate closely with other teams to meet quality standards and regulatory requirements.

Qualifications

• Bachelor degree in a relevant scientific field (e.g., Chemistry, Biology, Biomedical Engineering).
• Knowledge of cGMP and GDP in a pharma or biotech facility.
• Good understanding of drug development process.

Responsibilities

• Management of test samples including in-process and release samples.
• Stability sample management.
• Regulatory retain sample management.
• Reference sample management.
• Responsible for QC instrument and equipment management.
• Ensure compliance with cGMP, data integrity, and EHS requirements.

Skills

Knowledge of current Good Manufacturing Practices (cGMP)

Good interpersonal skills

Good communication skills

Good presentation skills

Strong Quality mindset

Education

Bachelor's degree in a relevant scientific field

Tools

HPLC

GC

IC

LC-MS

pH meter

balance

color meter

LIMS

EMPOWER

LES

Job description

Responsibilities:

• Management of test samples: In-process and release samples, environmental testing samples and drug substance and excipient samples.
• Stability sample management.
• Regulatory retain sample management.
• Reference sample management.
• Responsible for QC instrument and equipment management, like C type instruments including HPLC, GC, IC and LC-MS and B type instruments pH, balance and color meter.
• Responsible for electronic system application, including but not limit to LIMS, EMPOWER and LES.
• Ensure all the activities in QC team performed with compliance of cGMP, data integrity and EHS requirement.

Qualifications:

• Bachelor degree in a relevant scientific field(e.g., Chemistry, Biology, Biomedical Engineering, or related discipline).
• Knowledge of current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP) in a pharma or biotech facility.
• Good interpersonal, communication and presentation skills.
• Good understanding of overview view of drug development process.
• Strong Quality mindset.