Senior QC Scientist - Pharma MNC #HTJ

Recruit Express Pte Ltd; Singapore; On-site; SGD 60,000 - 90,000; Full time

Job summary

Recruit Express Pte Ltd is recruiting a QC Scientist for API pharmaceutical manufacturing based in Tuas Biomedical Park. This full-time role focuses on leading analytical troubleshooting and supporting method development, validation and transfer for active pharmaceutical ingredients.

You will operate HPLC, GC, LC-MS and other instruments, review data, prepare GMP-compliant reports and guide the laboratory team on critical projects.

Qualifications

• API pharmaceutical manufacturing experience is mandatory.
• Requires 5–12 years of QC/analytical experience.
• Degree or higher in Chemistry, Pharmacy, or Analytical Chemistry.
• Familiar with ICH, USP, EP and regulatory requirements.

Responsibilities

• Lead analytical troubleshooting and laboratory investigations.
• Support API analytical method development, validation and transfer.
• Operate and troubleshoot HPLC, GC, LC-MS and other analytical instruments.
• Review analytical data, prepare reports and ensure GMP compliance.
• Lead laboratory projects and provide technical guidance to team members.

Skills

Analytical troubleshooting

Instruments operation

Team guidance

Education

Chemistry/Analytical Chemistry degree

Tools

HPLC

GC

LC-MS

Job description

QC Scientist (API Pharmaceutical Manufacturing)

Employment Type: Full-Time
Location: Tuas Biomedical Park
Transport: Islandwide Company Transport

Job Scope:

• Lead analytical troubleshooting and laboratory investigations
• Support API analytical method development, validation and transfer
• Operate and troubleshoot HPLC, GC, LC-MS and other analytical instruments
• Review analytical data, prepare reports and ensure GMP compliance
• Lead laboratory projects and provide technical guidance to team members

Requirements:

• Degree / Master's / PhD in Chemistry, Pharmacy, Analytical Chemistry or related field
• API pharmaceutical manufacturing experience is mandatory
• Preferably 5-12 years of relevant QC / analytical experience
• Strong experience with analytical instruments and method troubleshooting
• Familiar with ICH, USP, EP and pharmaceutical regulatory requirement