Woolloongabba, Queensland, au Architecture and Engineering Occupations
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Staff Australia are currently seeking an experienced Quality Control Technician - Biochemistry to join our team for a role based in Woolloongabba, QLD.
Our client is a multi-product biopharmaceutical site with development and manufacturing facilities for pharmaceutical products for clinical trials (Phase l, ll and lll).
ASAP start Monday to Friday dayshift roster Attractive salary package
About your new role
Participate in activities related to analytical development and QC test strategy to meet or support the client's requirements and/or expectations
Ensure the execution of studies is according to current guidelines
Contribute to the maintaining of TGA and other licenses
Sound knowledge of equipment used for execution of test records (SoloVPE, qPCR, Binding ELISA, Endotoxin etc)
Assessment of analysis against predefined specification
Effective execution of test records for customer requirements
Peer review of analysis for completeness and correctness
Assist QC Supervisor in review/approval of test records, where relevant
Identify and report non-conformances and OOS/UR results directly to Supervisor, Senior Manager, QC or delegate
Contribute to the effective delivery of high value analytical services to clients
Understanding of the Quality Control practices and principles across the full spectrum of site manufacturing services
Support in the practical application of various risk assessments tools (i.e. failure mode effect analysis, fishbone diagrams, hazard and operability studies) and ability to directly develop, participate and advise others on the appropriate and efficient application of these processes
Support in the practical application of the Quality System, Change Control, Deviations, CAPA, OOS and OOT, Document Management, related to the Quality Control Department
Assist with site PPI projects
Perform any other legitimate duties as directed by the Senior Manager, QC (or delegate)
Bachelor of Science (Bio-Technology, Chemistry or closely related degree)
Post Graduate qualifications, beneficial
Specific knowledge of Bio-pharmaceutical processes, Pharmaceutical guidelines and principals of, preferred
Familiarity with principles of Aseptic techniques, preferred
At least 1 - 2 years' experience in the pharmaceutical and/or pharmaceutical industry aligned to Analytical and Quality Control fields
Knowledge in cGMP practices
Background in analytical theory and technical competency with laboratory analysis, desirable
Ability to work in a highly dynamic, frequently changing environment with a wide variety of people and perspectives
Proven record of the ability to work as a team and independently as required
Ability to effectively communicate in multiple modalities (e.g. electronic, written, verbal etc.)
Ability to work on multiple projects simultaneously and demonstrate initiative to complete tasks according to company milestones/goal tree
Strong team working and collaborative skills
Good knowledge of Microsoft applications (e.g. Excel, Word, Outlook, PowerPoint)
Good knowledge of Smartsheets, desirable
You may be required to undergo pre-employment Drug and Alcohol Screening as a requirement for this role.
If you feel you are suitable for this role, please upload a current resume by click on APPLY NOW!
Please note, only suitable applicants will be contacted.