Address
Form of workAbout Probiotec
Probiotec Limited is an ASX listed, fully Australian owned business leading the way in both contract manufacturing and packing services. As one of Australia’s largest full-service contract manufacturers, we provide best in class marketing, and distribution of diverse, high quality prescription and over-the-counter pharmaceuticals, complementary medicines, human nutrition, and specialty ingredients products.
The business is also one of Australia’s largest packing companies, offering a multitude of packing services – including primary, secondary & co-packing capabilities as an end-to-end manufacturing and packing partner. With multiple sites across Australia including Multipack LJM, South Pack Laboratories, ABS, HH Packaging, LJM and Probiotec Pharma, the group is responsible for employing over 1000 employees nationwide.
As a leader in Australian manufacturing and packing services, Probiotec provides innovative healthcare products that improve the lives and well-being of our customers.
About the Role
- To support the introduction of new production into productions, ensuring processes, documentation and in process quality checks are in place
- To assist the Quality Assurance Manager to implement and maintain Quality Systems, Quality Manual, Policies, Procedures and Specifications to ensure that all comply with company and regulatory authority requirements
- Reports to the Quality Assurance Manager
About You
- Independent and practical trouble-shooter
- Keen to co-ordinate and develop logical solutions with stakeholders
- Strong communication skills
- Excellent excel skills
Main Tasks
- To have a good understanding of TGA and HACCP regulatory requirements, and principles of quality assurance and control
- Conducting quality checks within production to ensure processes are correctly followed and product is produced as per customer requirements.
- Inspect incoming materials and products to ensure product quality.
- Inspect finished goods to ensure product quality.
- Perform internal GMP inspections and document corrective actions.
- To create product packing instructions for production department to enable the production of quality products which meet the customer specification.
- To provide training to production staff.
- Participate in customer audits/internal audits as required and assist with the implementation of corrective actions.
- Assist in preparing reports to communicate outcomes of quality activities.
- Has the authority to undertake “product for release to customer “step and has the authority to approve or reject materials and finished goods under guidance from the QA Manager.
- Has been trained to act as the Authorized Person and has been delegated the task of performing the Release for Supply manufacturing step as required.
- Ensure that any customer and/or other non-conformance issues raised are addressed within a timely manner and corrective actions are implemented and documented.
- To assist in ensuring that production quality documentation is developed in line with regulatory and customer requirements.
- To assist with the development, implementation and maintenance of the quality system and quality documentation
- To understand that personal medications are prohibited within the factory. For any special case, respective Manager must be advised.
- Adhere to EHS programs and support the EHS systems.
