Senior QC Scientist | API Analytical Testing & Method Development | Pharma Manufacturing | Tuas | Salary Negotiable #HYT

Recruit Express Pte Ltd; Singapore; Presencial; SGD 70.000 - 120.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Islandwide Company Transport

Descripción de la vacante

Recruit Express Pte Ltd is seeking a QC Scientist specialized in API pharmaceutical manufacturing, located at Tuas Biomedical Park. The role focuses on leading analytical troubleshooting, supporting method development, validation and transfer, and ensuring GMP compliance.

The candidate will operate HPLC, GC, LC-MS and other instruments, review data, prepare reports and guide laboratory projects. A degree or higher in related fields is required with 5–12 years of QC/analytical experience

Formación

• Degree or higher in Chemistry, Pharmacy, Analytical Chemistry or related field.
• API pharmaceutical manufacturing experience is mandatory.
• Strong experience with analytical instruments and method troubleshooting.

Responsabilidades

• 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.

Conocimientos

Analytical troubleshooting

Laboratory data analysis

HPLC/GC/LC-MS proficiency

GMP/compliance knowledge

Team guidance

Educación

Degree / Master’s / PhD in Chemistry or related field

Herramientas

HPLC

GC

LC-MS

Descripción del empleo

QC Scientist (API Pharmaceutical Manufacturing) | Tuas

Employment Type: Full-Time
Salary: Open, based on experience
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