Senior QC Chemist
Aegros Therapeutics Pty Ltd, Australia
Job Description
Aegros is Latin for ‘Patient’. We chose this name because it speaks to our focus on the patient. Every day we strive to place the patient first by providing therapeutic plasma products they would not otherwise be able to access.
At Aegros we believe access to life saving therapeutic plasma drugs is a human right and not a privilege. In a nutshell our mission is to put the patients first through innovation.
Over 30 years we have developed our HaemaFrac process which enables countries to turn human plasma they collected into life saving hyperimmune products.
It's no secret that Aegros is expanding rapidly! An exciting opportunity has arisen for a Senior QC Chemist to join our Quality Compliance team. Working with the QC team you will be primarily focussing on planning and executing method validation, verification, and improvements to method functionality.
What you will be involved in
- Undertaking method development and validation on analytical equipment
- Validating and assessing biochemistry testing including ELISA, electrophoresis, flow cytometry, nephelometry, auto-coagulation, haemagglutination, etc
- Ensuring all GMP, Safety, Corporate, Regulatory and legislative compliance requirements are met
- Generating validation protocols and reports ensuring practices
- Performing tests for validation activities associated with changes to existing and new processes
- Writing technical reports, developing validation plans, SOPs, programs and policies
- Ensuring equipment and facilities are maintained and calibrated following approved procedures and perform troubleshooting in the case of equipment malfunction
- Managing audit preparations and provide support in areas of validation
- Performing any other duties assigned by manager or delegates
- Flexible to work is shifts across the day on a rotating roster.
Requirements
What we would expect from you:
- A Bachelor of Science degree preferably in Chemistry, Pharmaceutical science or related fields
- 4-8 years’ experience in microbiological testing and analysis in QC laboratory as an analyst in pharmaceutical or related industries
- Demonstrated experience within chromatographic method development and validation to ICH standards
- Proficient with MS Excel amp; Word
- Prior experience working within the pharmaceutical industry is highly desirable
- Proven experience within method development and validation
- Excellent written and verbal communication skills
- Able to work autonomously while also being a part of a team.
- Performing any other duties assigned by manager or delegates.
- Flexible to work is shifts across the day on a rotating roster.
Benefits
Here’s what we can offer you
- An environment which allows the individual to grow alongside the company
- A role that provides the bandwidth to explore innovative solutions while keeping patients at the centre of everything we do
- The chance to work with global industry experts in an organisation where success will be defined not just on successful delivery of goals but on how they were achieved
- A multicultural environment where every voice is heard
- Competitive remuneration package which includes an annual Bonus + Employee Share Options
- Close to public transport
Interested? Apply today...!