Laboratory Analyst (1 year contract)

GlaxoSmithKline plc

Sydney

On-site

AUD 55,000 - 85,000

Full time

6 days ago
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Job summary

GSK is seeking an Analytical Chemist / Microbiologist to ensure accurate testing of raw materials, samples and final products in a cGMP environment. You will support non-order fulfilment, resolution of process issues and introduction of new analytical tests.

You will maintain instruments, reagents, and documentation, operate ERP/LIMS/Empower systems, and uphold a safe, well-organized lab with high data integrity and teamwork.

Qualifications

  • GCE O/A Level or Diploma in Chemical Process Technology/Applied Chemistry.
  • Minimum 2 years in analytical environment; pharma preferred.
  • Open to fresh graduates; willing to work 12-hour shifts.
  • Good knowledge of GMP and GLP; knowledge of analytical techniques and lab instrumentation.

Responsibilities

  • Analyze and test raw materials, factory samples, intermediates, final products and utilities per quality requirements.
  • Ensure instruments, reagents and standards are in proper working order and within expiry; regulatory compliant documentation.
  • Operate lab computer applications (ERP, LIMS, Empower) to complete system transactions.
  • Maintain housekeeping in the laboratory and ensure a safe working environment; perform 6S inspections.
  • Communicate findings and contribute to investigations and problem-solving as part of lab operations.

Skills

Data Integrity
Detail-Oriented
Digital Fluency
GxP Regulations
Lean Management
Problem Solving
Quality Assurance
Quality Control
Risk Awareness
Testing Operations

Education

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

Tools

LIMS
CDS
Corporate ERP System
Empower

Job description

  • 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

1. 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.

2. Ensure that all instruments are in good working order, reagents and reference standards within expiry and that documents meet regulatory standards.

3. 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.

4. Maintain an excellent standard of housekeeping in the laboratory.

5. Ensure a safe working environment in the laboratory and perform 6S inspection.

Key Requirement
  • 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
  • Good teamwork
  • People management skills (SLA and SLA3)
Skills
Data Integrity, Detail-Oriented, Digital Fluency, GxP Regulations, Lean Management, Problem Solving, Quality Assurance (QA), Quality Control (QC), Risk Awareness, Testing Operations
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

1. 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.

2. Ensure that all instruments are in good working order, reagents and reference standards within expiry and that documents meet regulatory standards.

3. 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.

4. Maintain an excellent standard of housekeeping in the laboratory.

5. Ensure a safe working environment in the laboratory and perform 6S inspection.

Key Requirement
  • 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 ***************@gsk.com. 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.

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