Analytical Project Leader - Rutherford, Australia - Zoetis

Zoetis

Verified Company

Rutherford, Australia

3 weeks ago

Posted by:

Olivia Brown

beBee Recruiter

Description

Position summary

The role is primarily responsible for the development and implementation of robust analytical methods and analytical projects in support of small molecule veterinary pharmaceutical products for domestic and international markets.

To provide practical analytical expertise to project teams, taking account of current regulations and trends. Employing good documentation and data practices for knowledge management, retention, and transfer of new or improved methods or processes.

Provide support to the development and maintenance of technical capability and competency of colleagues, aligned to the quality standards and regulations.

Position responsibilities

Carry out agreed projects to manage and conduct analytical development to produce effective methodologies and analytical capability.
Practical Analytical development, data review and documentation management in accordance with appropriate quality and regulatory requirements such as ICH, VICH, FDA, APVMA, NATA.
Operation of analytical instruments to generate data and knowledge of robust analytical methods documented to support product dossier development and technology transfer.
Actively support team to develop and grow their analytical competencies, to plan for and ensure that individual and group analytical skills, knowledge and capability are to a high standard and capable of meeting our global ambition.
Evaluation of new techniques and technologies in consideration of improvement of quality attributes and efficiency of process flows. Ability to contribute to the VMRD global analytical development efforts as appropriate.
Use and adoption of practices or procedures to ensure adequate quality standards can be and are continuously met.
Observe and follow relevant GxP, regulatory and safety guidelines.

Education and experience

Tertiary degree in Science or Engineering. Chemistry preferred.
Minimum of 8 years' experience in pharmaceutical research or analytical development.

Technical skills requirements

Practical analytical skills in Chromatographic techniques, HPLC in particular, for method development, robustness, validation and technical transfer of commercially viable analytical methods.
Organisational and Project Management competencies.
Working knowledge of current technologies and trends in pharmaceutical Analysis, Regulator and Quality expectation and frameworks (ICH, VICH, FDA, APVMA, NATA)