About the Company

Our client is one of the world’s leading global pharmaceutical manufacturers and suppliers of pharmaceutical related products for the local and export overseas market.

Due to new project requirements, our client is now seeking a QC Instrument Validation Associate to be responsible for instrumentation qualification and data analysis of laboratory computer based equipment.

About the Role

Reporting to the QC Manager, key accountabilities include the following:

- Write and execute instrument qualifications including data integrity.
- Review & prepare qualification documentation & execution of documents.
- Perform testing to ensure systems are working as intended - lab equipment such as UVV, GC. plate reader & particle counters etc.
- Update SOPs, validation protocols & technical documents in relation to qualification and lifecycle management.




- Effectively liaise with internal & external key stakeholders in relation to computerised laboratory equipment.

About you

You will be a self-starter with the following skills and experience:

- Tertiary qualifications in Science, IT or Computer Systems.
- Minimum 2 years of experience.
- Sound experience with instrument qualification of lab equipment.
- Industry experience in pharmaceutical/biotech industry.
- Experience in compliance with cGMP, GLP, GxP and Laboratory quality systems & requirements.
- Knowledge and understanding of GMP regulations.

Additional information

- Global Pharmaceutical Manufacturer
- Excellent Long Term Contract Prospect
- Melbourne Metro Area

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📌 QC Instrument Validation Associate (Melbourne)
🏢 Bell People Consultants
📍 Melbourne