Mavlab is a privately owned and operated Australian company specialising
in the design, development and manufacturing of animal health products.
Established in 1970, we offer one of the most comprehensive ranges in the
industry-covering everything from everyday essentials to specialist
therapeutics.
We manufacture trusted over-the-counter and prescription medications-from joint
care and anxiety to epilepsy and heart health. Our range includes tablets,
liquids, powders, injectables, as well as grooming products such as
shampoos and conditioners.
Working with leading with leading partners-locally and internationally-we
research, formulate, and deliver results-driven products that meet the real-
world needs of pet owners and veterinary professionals alike.
Your responsibilities will include:
* Maintain Quality Assurance documentation and databases.
* Assist in raw material review and release for manufacturing
* QA sign-off on received packaging, review any supporting certification (Assist RM)
* Prepare/revise Mavlab’s packaging specification
* Check/review printed packaging specifications (prepared by LPO)
* Create/revise Contract packaging spec and send for client's approval (including printed packaging
* Create label specs
* Perform barcode verification and allocation
* Create raw and packaging material specifications, item cards, BOM, and Route
* Trending and Reporting of purified water system results to relevant stakeholders
* Assist with air Pressure Monitoring / Temperature Monitoring and generate graphs.
* Apply release green sticker for Packaging and Finished Products
* Create and review Navision production documentation to ensure document accuracy and consistency.
* Enter and review test results into the manufacturing results database and review for trends in product quality.
* Batch document review
* Release for supply of registered and non-registered finished goods.
* Perform line clearances.
* Assist in the management and facilitation of actions relating to Control of Change
* Generate NCR’s, control of change, OOS, deviations and manage the database for completion.
* Record reported batch deviations
* Manage, write and update SOP’s and other controlled documents to meet current regulatory and quality standards.
* Assist the QA Manager with updating, indexing and recording GMP contracts.
* Assist the QA department in maintaining its quality system certification and legislative requirements.
* Monitor in house hygiene practices, and staff compliance ensuring compliance to relevant GMP guidelines.
We would love to hear from you if you have experience in the above and you want to work in a business where the values are real and not just words on a wall.