Senior / QC Associate - Projects (2-Years Contract)

You will join our Quality Control team in Singapore as a Senior / QC Associate (Projects). You will perform analytical testing, manage samples, and support project work that keeps our manufacturing and laboratory activities compliant and on schedule. You will work closely with laboratory colleagues, production and quality partners. We value accuracy, clear communication and a collaborative mindset. This role offers hands-on technical growth, project exposure, and the chance to contribute to GSK’s mission of uniting science, technology and talent to get ahead of disease together.

Responsibilities

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

• Perform testing for project related activities for intermediates/ products to meet quality and regulatory standards.

• Manage sample receipt, triage, storage, chain of custody and disposition to ensure traceability and sample integrity.

• Support method development, verification, validation and transfer activities and take part in laboratory investigations when needed.

• Operate, calibrate and perform basic troubleshooting for laboratory equipment; arrange maintenance with vendors as required.

• Lead or support project tasks such as process improvements, documentation updates and continuous improvement initiatives.

• Maintain accurate, timely records and follow good documentation and laboratory practices to ensure inspection readiness.

Why You? Basic Qualification

We are seeking professionals with the following required skills and qualifications to help us achieve our goals

• Diploma or degree in Chemistry, Biology, Biochemistry, Biotechnology or a related life science field.

• Minimum of 2 years of laboratory experience in an analytical or QC environment.

• Practical knowledge of good laboratory practices and good documentation practices.

• Able to work on-site in Singapore (this role is on-site).

• Clear written and spoken English with accurate documentation skills.

• Able to work independently and as part of a team and to follow shift patterns when required.

Preferred Qualification If you have the following characteristics, it would be a plus

• Experience with chemistry testing techniques, biochemical assays or analytical instrumentation.

• Knowledge of good manufacturing practice (GMP), good laboratory practice (GLP) and laboratory safety.

• Familiarity with laboratory information systems (LIMS) or electronic data management.

• Experience leading investigations, corrective actions (CAPA) and continuous improvement activities.

• Ability to train colleagues and contribute to team development.

• Proficiency with Excel and basic data analysis for trending and reporting.

To learn more about Singapore GSK and our people, please click on this link:  https://www.linkedin.com/company/glaxosmithkline/life/gsksingapore #Li-GSK