Qc Analyst
1 week ago
- Excellent Long Term Contract Opportunity
- Melbourne Metropolitan Area
About the Company:
Operating as a major global Multinational pharmaceutical manufacturer with global sites worldwide, our client is well known for its growth and innovation and is an Australian iconic brand in the marketplace, offering a range of healthcare products to local & global markets.
QC Analyst with experience in writing laboratory procedures & method development and validation within a cGMP environment.
About the Opportunity:
Key responsibilities include the following:
- Review & write laboratory procedures in accordance with regulations & guidelines.
- Be responsible for method validation & writing of protocols & reports.
- Use laboratory instruments such as Chromatograpahy for testing & data analysis work.
- Ensure equipment & facilities are maintained & calibrated in accordance with approved procedures.
- Ensure all documents are recorded in the Quality Management Systems.
- Effectively liaise with internal stakeholders at all levels.
About You:
- Tertiary qualifications in Science.
- Minimum 2 years of experience in method development/method validation within cGMP environment.
- Sound understanding of aspects of analytical method lifecycle management.
- Experience in chromatography & cGMP testing.
- Experience with quality document management systems & LIMS.
- Sound written & verbal communication skills.
Culture & Benefits
This is an excellent contract opportunity for a
talented and self motivated QC Analyst with Method Validation & Development to join a leading global pharmaceutical manufacturing organisation & be involved in writing of lab procedures & protocols.
How to Apply
CV in MS Word.
For confidential discussion, you can contact Sue Campbell on
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