Benefits - Be part of a supportive and stable working environment
- Working within a global team
- Must have own car and licence
About the company Work within a large global Biotechnology company that boasts a good company culture that is always expanding.
About the opportunity The Quality Assurance Associate will be responsible for all activities involving quality assurance and compliance with applicable regulatory requirements; conducting audits and reviewing/analyses data and documentation. This is a Full-time 3-month contract opportunity based near Melbourne Airport.
Duties - Undertake specific tasks for project – reviews for site project
- Create checklists, pull information from various sources to form a checklist for the stage gate reviews to move to next stage of project
- Person will need to talk to different areas of the business to get information needed
- Checking of items listed in checklist have been completed and document that they have been completed
- There is a lot of data to pull from many sources
- Will need to take charge and run with the tasks
- Review procedures and write some documents
Skills and Experience - Must have a Science Degree in a relevant discipline (Quality related Science degree)
- Minimum of 2 years’ experience in a regulated industry with a focus on QA and cGMP, e.g. pharmaceutical manufacturing or R&D
- Experience in Microsoft Word, PowerPoint, Excel and Visio
- Experience in the operation of Quality Management Systems / Pharmaceutical Quality System or equivalent
- Able to work closely with others to ensure the success of quality on the floor
- Demonstrated ability for analytical thinking with sound judgement
- Ability to work well independently and to self-motivate
Culture Although a large, global company, they are able to provide a family-like culture and pride themselves in improving the lives of others.
How to Apply Click apply or contact Jo Turner – Senior Specialist Manager on 03 9938 7120 for a confidential discussion.#J-18808-Ljbffr