QA Analyst (Pharma MNC, 8m contract, office hours) #HAC

RECRUIT EXPRESS PTE LTD; Singapore; On-site; SGD 42,000 - 66,000; Full time

Job summary

RECRUIT EXPRESS PTE LTD in Singapore seeks a QC Analyst to perform routine QC testing of raw materials, in-process and finished products in accordance with SOPs and cGMP. You will conduct analytical testing using HPLC, CE-SDS and icIEF, use Empower CDS for data acquisition, processing and documentation, and support method transfer, validation, equipment qualification and troubleshooting.

Strong documentation skills and commitment to data integrity are essential, with hands-on GMP QC laboratory

Qualifications

• Diploma/Degree in Chemistry, Biochemistry, Biotechnology, Pharmaceutical Science or related discipline.

Responsibilities

• Perform routine QC testing of raw materials, in-process and finished/bulk products in accordance with SOPs and cGMP requirements.
• Conduct analytical testing using HPLC, CE-SDS and/or icIEF and other relevant analytical/biochemistry techniques.
• Use Empower CDS for chromatographic data acquisition, processing, review and documentation.
• Support method transfer, method validation, equipment qualification and analytical troubleshooting.
• Ensure accurate and timely documentation of test results in compliance with GMP and data integrity requirements.
• Support laboratory activities including equipment maintenance, inventory management and general lab operations.

Skills

QC testing

Analytical thinking

Documentation

Education

Diploma/Degree in Chemistry, Biochemistry, Biotechnology, Pharmaceutical Science or related discipline

Tools

HPLC

Empower CDS

CE-SDS

icIEF

Job description

Key Responsibilities

• Perform routine QC testing of raw materials, in-process and finished/bulk products in accordance with SOPs and cGMP requirements.
• Conduct analytical testing using HPLC, CE-SDS and/or icIEF and other relevant analytical/biochemistry techniques.
• Use Empower CDS for chromatographic data acquisition, processing, review and documentation.
• Support method transfer, method validation, equipment qualification and analytical troubleshooting.
• Ensure accurate and timely documentation of test results in compliance with GMP and data integrity requirements.
• Support laboratory activities including equipment maintenance, inventory management and general lab operations.

Requirements

• Diploma/Degree in Chemistry, Biochemistry, Biotechnology, Pharmaceutical Science or related discipline.
• Hands-on experience with HPLC and Empower is highly preferred.
• Experience with CE-SDS and/or icIEF will be advantageous.
• Prior GMP QC laboratory experience within pharmaceutical/biologics manufacturing is preferred.
• Good understanding of analytical testing, documentation and laboratory practices.