GSK

Biopharma

Senior/QCAssociate-Projects(2-YearsContract)

S$78–115k ~AI est. Singapore, Singapore FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“Senior / QC Associate - Projects (2-Years Contract) at GSK. Skills: Analytical testing, Sample management, Method development, Method validation. Perform testing for project related activities. Manage sample receipt”

Industry & Context.

Biopharma
Problems you'll solve

Basic troubleshooting; Laboratory investigations; Corrective actions

Eligibility Requirements

On-site work required

What They're Looking For.

Must Have

Diploma or degree in Chemistry, Biology, Biochemistry, Biotechnology or related life science field, Minimum of 2 years laboratory experience in analytical or QC environment, Practical knowledge of good laboratory practices, Practical knowledge of good documentation practices, Able to work on-site in Singapore, Clear written and spoken English, Accurate documentation skills, Able to work independently, Able to work as part of a team, Able to follow shift patterns

Nice to Have

Experience with chemistry testing techniques, Experience with biochemical assays, Experience with analytical instrumentation, Knowledge of good manufacturing practice (GMP), Knowledge of good laboratory practice (GLP), Knowledge of laboratory safety, Familiarity with laboratory information systems (LIMS), Familiarity with electronic data management, Experience leading investigations, Experience leading corrective actions (CAPA), Experience leading continuous improvement activities, Ability to train colleagues, Ability to contribute to team development, Proficiency with Excel, Basic data analysis for trending and reporting

What You'll Do.

Perform testing for project related activities

Manage sample receipt

Manage sample storage

Manage sample chain of custody

Manage sample disposition

Support method development

Support method verification

Support method validation

Support method transfer

Take part in laboratory investigations

Operate laboratory equipment

Calibrate laboratory equipment

Perform basic troubleshooting for laboratory equipment

Arrange maintenance with vendors

Support project tasks

Initiate continuous improvement initiatives

Maintain accurate records

Maintain timely records

Follow good documentation practices

Follow good laboratory practices

How You'll Work.

Team & Collaboration

Work closely with laboratory colleagues; Work closely with production partners; Work closely with quality partners

Communication Scope

Written English; Spoken English; Documentation skills

Process & Methodology

Process improvements, Documentation updates, Continuous improvement initiatives

Full Job Description

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 spok

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