Analyst, Quality Control

Randstad – Lonza; Singapore; On-site; SGD 60,000 - 90,000; Full time

Benefits offered by this job

Medical insurance

Transport from MRT to Tuas site

Career growth opportunities

Job summary

Randstad – Lonza in Singapore is seeking a QC Analyst to support Biochemistry in the QC Lab for Lot Release activities. You will prioritize and perform analytical testing to meet deadlines, and ensure methods are executed per SOPs.

The role requires a degree with 5 years QC/Quality experience in biopharmaceuticals; familiarity with FDA/EMEA/ICH and GMP; strong documentation, communication, and teamwork. Willing to do 12-hour shift at the Tuas site.

Qualifications

• Degree or higher with 5 years of QC/Quality experience in biopharmaceuticals.
• Familiarity with FDA, EMEA, ICH guidelines and GMP quality systems.
• Strong planning, prioritization, and documentation skills.
• Lab experience in biotech or medically related fields preferred.

Responsibilities

• Prioritize and perform analytical testing to meet timelines
• Test final product, in-process, and stability samples per SOPs and methods
• Document and review results in compliance with cGMP and data integrity requirements
• Execute methods such as ELISA, PCR, CE, SDS-PAGE, IEF/icIEF, potency, and other physicochemical assays
• Support general lab operations: housekeeping, equipment upkeep, inventory, autoclaving, and glassware management
• Prepare and maintain standards/reagents based on GMP requirements
• Troubleshoot analytical methods and equipment issues
• Participate in equipment qualification and maintenance
• Support or lead OOS and deviation investigations; draft reports
• Train others on test methods
• Contribute to method transfer and validation activities
• Author change controls, test methods, and SOPs

Skills

Analytical testing

Documentation

Communication skills

Quality mindset

Team player

Education

Bachelor’s degree in Biochemistry/related field

Tools

ELISA

PCR

CE

SDS-PAGE

IEF/icIEF

Potency assays

Job description

The QC Analyst will be responsible for Biochemistry Area in the QC Lab to support Lot Release activities

What you’ll get

An agile career and dynamic working culture in a global life sciences leader.

An inclusive and ethical workplace that values diversity and integrity.

Competitive compensation programs that recognize high performance.

Professional growth opportunities through cross-functional projects and global exposure.

Comprehensive medical insurance, with the option to enroll family members at partially subsidized premiums.

Company transport provided from designated MRT locations to and from the Tuas site.

Access to Lonza’s full suite of employee benefits: www.lonza.com/careers/benefits

Willing to do 12hours Shift role

What you’ll do:

Prioritize and perform analytical testing to meet business timelines

Test final product, in-process, and stability samples per SOPs and methods

Document and review results in compliance with cGMP and data integrity requirements

Execute methods such as ELISA, PCR, CE, SDS-PAGE, IEF/icIEF, potency, and other physicochemical assays

Support general lab operations: housekeeping, equipment upkeep, inventory, autoclaving, and glassware management

Prepare and maintain standards/reagents based on GMP requirements

Troubleshoot analytical methods and equipment issues

Participate in equipment qualification and maintenance

Support or lead OOS and deviation investigations; draft reports

Train others on test methods

Contribute to method transfer and validation activities

Author change controls, test methods, and SOPs

What we’re looking for:

Degree or higher with 5 years of QC/Quality experience in biopharmaceuticals

Preferably lab experience in biotech or medically related fields

Familiarity with FDA, EMEA, ICH guidelines and GMP quality systems

Strong planning, prioritization, and documentation skills

Good communication and interpersonal abilities

Analytical, meticulous, and quality-focused mindset

Team player who can work independently with strong safety and timeline discipline

Openness to new challenges and continuous improvement