Laboratory Analyst (1 year contract)

GSK; Singapore; On-site; SGD 60,000 - 85,000; Full time

Job summary

GSK Singapore seeks an analytical support professional to assist the Analytical Chemist/Microbiologist in testing raw materials, intermediates, and final products to ensure cGMP and regulatory compliance. The role supports measurements, instrument maintenance, and resolution of process/method issues, with the introduction of new measurement technologies and tests.

You will lead, schedule, and test various samples and ENVOPS in accordance with procedures, while maintaining data integrity and

Qualifications

• GCE O’ or A’ Level in relevant subjects and/or Diploma in Chemical Process Technology or Applied Chemistry.
• Minimum 2 years of experience in an analytical environment, preferably pharmaceutical.
• Open to fresh graduates.
• Willing to work a 12-hour shift pattern.
• Strong GMP/GLP knowledge.
• Familiar with analytical techniques, equipment capabilities, and operations.
• Knowledge of microbiological testing.

Responsibilities

• Analyze and test raw materials, intermediates, finished products, and utilities as per quality requirements.
• Ensure instruments are functional, reagents valid, and documents meet regulatory standards.
• Operate laboratory software (ERP, LIMS, Empower) and maintain training records.
• Maintain high housekeeping standards in the laboratory.
• Maintain a safe working environment and perform 6S inspections.

Skills

Communication skills

Teamwork

Problem solving

People management (SLA)

Detail-oriented

Digital fluency

GxP Regulations

Quality Assurance (QA)

Quality Control (QC)

Risk awareness

Education

GCE O/A Level or Diploma in Chemical Process Technology or Applied Chemistry

Tools

CDS

LIMS

ERP System

Job description

Job Purpose

To assist the Analytical Chemist / Microbiologist to ensure that all utilities (water, environmental and compressed gas), process raw materials, factory samples, intermediates and final products are analysed and the results recorded in full compliance with current Good Manufacturing Practice (cGMP) and regulatory requirements that meets the defined quality standards. In addition, provide analytical support for non-order fulfilment activities required for the resolution of process and method problems / issues, and the introduction of new measurement technologies and analytical tests. To lead, schedule and test Value Stream specific raw materials, process intermediates, final product, non-routine samples and ENVOPS in accordance to written procedures and methods.

Key Responsibilities

• Ensure that all raw materials / factory samples / intermediates / final products / utilities microbiological monitoring / non-order fulfillment and NCE fulfillment activities are analyzed and tested according to the stipulated quality requirements so as to provide accurate test results for correct usage decisions.
• Ensure that all instruments are in good working order, reagents and reference standards within expiry and that documents meet regulatory standards.
• Operate the relevant computer applications that are related to the laboratory functions, such as Corporate ERP System, LIMS, Empower and other network operating systems, as required to ensure completion of Corporate ERP System transactions. Use the appropriate documentation system for the activities being carried out Ensure training records keep up to date.
• Maintain an excellent standard of housekeeping in the laboratory.
• Ensure a safe working environment in the laboratory and perform 6S inspection.

Key Requirements

• GCE ‘O’ or ‘A’ Level in relevant subjects and/or Diploma in Chemical Process Technology or Applied Chemistry
• Minimum 2 years of experience in an analytical environment, preferably in the pharmaceutical industry
• Open to fresh graduates
• Must be open to 12-hour shift work pattern
• Good knowledge of GMP and GLP
• Good knowledge of analytical techniques, equipment capabilities and operational needs
• Good knowledge of microbiological testing
• Understanding product specification and method of analysis
• Knowledge of laboratory instrumentation CDS, LIMS and Corporate ERP System knowledge
• Investigation procedure
• Good communication skills
• Good teamwork
• People management skills (SLA and SLA3)
• Problem solving skills (Troubleshooting skills)
• Internal customer management skills
• Skills Data Integrity, Detail-Oriented, Digital Fluency, GxP Regulations, Lean Management, Problem Solving, Quality Assurance (QA), Quality Control (QC), Risk Awareness, Testing Operations

Why GSK?

Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines.

We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most.

Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

We are committed to creating an inclusive workplace and providing equal opportunities for all applicants. We embrace an agile working culture across our roles, so if flexibility is important to you please discuss opportunities with our hiring team.

If you need any adjustments to the recruitment process to help you demonstrate your strengths and capabilities, contact [e-mail]. Please note this email is for adjustment requests only; for other enquiries please use our standard contact channels.

Important notice to Employment businesses/ Agencies: GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together. Find out more on our career site.