QC Analyst
- Perform microbiological testing, sample processing and result interpretation in a pharmaceutical quality control laboratory.
- Maintain accurate GMP-compliant records and use LIMS and laboratory equipment to manage samples and results.
- Support laboratory operations, investigations, equipment maintenance and continuous improvement.
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
If you have a scientific background and experience working within a regulated laboratory environment, we'd love to hear from you. Apply today with your current resume.
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