QC Analyst

Manpower Australia; Melbourne; On-site; AUD 58,000 - 69,000; Full time

Benefits offered by this job

Long-term contract

Pharma manufacturer

Supportive team

Weekday hours

Immediate start

Graduate friendly

Job summary

Manpower Australia is partnering with a leading pharmaceutical manufacturer to appoint a QC Analyst (Microbiology) in Broadmeadows, VIC. The role is a contract through to June 2027, based on a Monday–Friday 36.75-hour week schedule, with an immediate start.

You will support the QC microbiology team in a GMP-regulated environment. Reporting to the QC Team Leader, you will perform testing, documentation and data entry, and help maintain laboratory systems and equipment.

Qualifications

• Tertiary qualification in Microbiology, Biotechnology, Biomedical Science, Chemistry or a related discipline.
• Experience in a Pharmaceutical Quality Control Laboratory.
• Strong understanding of GMP and GLP requirements.
• Experience operating laboratory instrumentation and equipment.
• Proficiency with Windows-based software and laboratory information systems.
• Excellent attention to detail and documentation skills.
• Strong communication and time management abilities.
• Ability to work effectively within a team and follow detailed procedures.

Responsibilities

• Perform microbiological testing, sample processing and result interpretation.
• Read and enumerate environmental monitoring and microbiological samples.
• Process and maintain sample records using LIMS and other laboratory systems.
• Conduct accurate data entry and documentation in accordance with GMP requirements.
• Operate, maintain and troubleshoot laboratory equipment.
• Coordinate the receipt, distribution and tracking of laboratory samples.
• Assist with stock control, ordering of consumables and laboratory housekeeping.
• Support investigations into atypical, invalid or out-of-specification results.
• Participate in equipment maintenance, calibration and continuous improvement activities.
• Ensure all work is completed in accordance with approved procedures and quality standards.

Skills

GMP/GLP experience

Lab testing

Data entry

Team collaboration

Attention to detail

Windows software

Education

Science degree in Microbiology / Biotechnology / Biomedical Science

Tools

LIMS

Laboratory instrumentation

Job description

QC Analyst (Microbiology) | Pharmaceutical Manufacturing

Location: Broadmeadows, VIC
Start Date: Immediate Start
Duration: Contract through to June 2027
Hours: Monday to Friday | 36.75 hours per week

Our client, a leading pharmaceutical manufacturing organisation, is seeking a QC Analyst to join their Quality Control Microbiology team. This is an excellent opportunity for a science graduate or experienced laboratory professional looking to build their career within a GMP-regulated environment.

About the Role

Reporting to the QC Team Leader, you will be responsible for performing microbiological testing, sample processing, laboratory documentation and supporting the day-to-day operations of a busy quality control laboratory.

Key Responsibilities

• Perform microbiological testing, sample processing and result interpretation
• Read and enumerate environmental monitoring and microbiological samples
• Process and maintain sample records using LIMS and other laboratory systems
• Conduct accurate data entry and documentation in accordance with GMP requirements
• Operate, maintain and troubleshoot laboratory equipment
• Coordinate the receipt, distribution and tracking of laboratory samples
• Assist with stock control, ordering of consumables and laboratory housekeeping
• Support investigations into atypical, invalid or out-of-specification results
• Participate in equipment maintenance, calibration and continuous improvement activities
• Ensure all work is completed in accordance with approved procedures and quality standards

Skills & Experience

• Tertiary qualification in Microbiology, Biotechnology, Biomedical Science, Chemistry or a related scientific discipline
• Previous experience within a Pharmaceutical Quality Control Laboratory
• Strong understanding of GMP and/or GLP requirements
• Experience operating laboratory instrumentation and equipment
• Proficiency with Windows-based software and laboratory information systems
• Excellent attention to detail and documentation skills
• Strong communication and time management abilities
• Ability to work effectively within a team and follow detailed procedures

What's on Offer

• Long-term contract through to June 2027
• Opportunity to gain experience with a leading pharmaceutical manufacturer
• Supportive team environment
• Monday to Friday roster with consistent hours
• Immediate start available
• Excellent opportunity for graduates with relevant laboratory experience