Qc Analyst

1 week ago

Melbourne, Australia Bell People Consultants Full time

Global Pharmaceutical Manufacturing Organisation
- 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.

Due to increase in project requirements within the quality team, our client is now seeking a
** 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 t**o 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 0417 994917.

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