Quality Control Analyst

SCG CELL THERAPY PTE. LTD.; Singapore; On-site; SGD 40,000 - 60,000; Full time

Job summary

A clinical-stage biotechnology company in Singapore seeks a candidate to perform routine QC assays, support laboratory operations, and contribute to process improvements. The ideal candidate has a diploma or degree in life sciences, and experience in cleanroom environments is preferred. This role offers a chance to impact the QC processes and grow within a fast-growing organization.

Qualifications

• Candidates with cleanroom experience preferred.
• Experience with cleanroom environmental monitoring would be advantageous.
• Experience with regulatory audits is a plus.

Responsibilities

• Conduct scheduled in-process and product release testing.
• Evaluate test data and generate test reports.
• Conduct environmental monitoring of cleanrooms.
• Draft standard operating procedures and QC related work instructions.
• Support routine QC laboratory operations.
• Contribute to the continuous improvement of QC procedures and processes.
• Assist in the development, optimization and qualification of new test methods.
• Apply good documentation practices on all records.

Skills

Cleanroom experience

Assay development

Environmental monitoring

Experience with cell and tissue cultures

Experience with flow cytometry

Experience with qPCR

Good documentation practices

Education

Diploma or Degree in chemical or life sciences

Job description

About SCG

SCG Cell Therapy Pte Ltd is a Singapore based clinical-stage biotechnology company focusing on the development of novel immunotherapies for patients with pathogenic infections and associated cancers.

WHAT WE'LL OFFER YOU

• The opportunity is based at the global headquarters of a fast-growing pre-IPO company dedicated to making positive differences in people's health. SCG is a company that provides employees with clear motivational goals and has a strong and positive employer brand in our field.
• A chance to develop your skills and advance in your career in a rapidly evolving business environment. This position is new in our organization, and thus you will have an excellent opportunity to impact the role and its responsibilities, build up a strong team and grow together with the company. This position offers significant career growth opportunity as the business is entering into a fast growth phase and high visibility to senior level management.
• A culture that is transparent, ambitious, international and where a team of experienced professionals with diverse backgrounds share a passion for helping patients and families in need.

Job Description

The candidate will perform routine assays and assist the QC team leader in validating new assays used for in-process and final product release testing. The candidate will also be expected to support the routine maintenance and upkeep of the QC laboratory, and contribute to the continuous improvement of QC processes.

Core responsibilities

• Conduct scheduled in-process and product release testing
• Evaluate test data and generate test reports
• Conduct environmental monitoring of cleanrooms
• Draft standard operating procedures and QC related work instructions
• Support routine QC laboratory operations
• Contribute to the continuous improvement of QC procedures and processes
• Assist in the development, optimization and qualification of new test methods
• Apply good documentation practices on all records

Role requirements

• Diploma or Degree in the chemical or life sciences
• Candidates with cleanroom experience preferred
• Experience with cleanroom environmental monitoring would be advantageous
• Experience with cell and tissue cultures, flow cytometry, qPCR and plate-based fluorescence assays would be advantageous
• Assay development experience is a plus
• Experience with regulatory audits is a plus
• Candidates familiar with GDocP, cGMP, and GLP principles preferred