AddressAbout the company:
Complementary Medicines Group (CMG) is a service provider to the complementary medicine, food and over-the-counter pharmaceuticals industries. We are TGA, FDA and BRC licensed.
We are based in the heart of Australia's “Vitamin Valley” Warriewood, NSW.
Our clients are well-known leaders in the natural health industry across Australia and ship to the US, UK, Europe, and more.
We are an Australian-owned company established in 2011 and are growing quickly, developing formulas crafted to our client's requirements, drawing on our team's knowledge and experience to create new and exciting products.
The Role:
Reporting to the head of Regulatory Affairs, you will be responsible for ensuring introduction of new products to the factory flows smoothly for a fast-growing company in the complementary medicines industry and its customers, adhering to company standards and the requirements of regulatory bodies e.g. the TGA.
Your experience working as part of a team within a fast paced and deadline-driven environment will see you excel in this role.
Your key responsibilities will include:
- Liaise with clients and suppliers regarding product development projects
- Formulate products in accordance with company quality and efficacy expectations
- Produce bench samples in the laboratory according to GLP
- Conduct general product and stress testing to ensure formulation robustness and efficacy claims compliance
- Report writing for justifications and supporting evidence for new product development projects
- Research based project management to ensure projects meet their required timelines
- Communicate the status of new product development to Business Managers and Project Managers
- Develop and maintain Master Formulas for all products that are manufactured within the
- company
- Collate the documentation data set from raw material suppliers for all new materials to be qualified into the approved list.
- Provide technical information to project managers, business managers, quality assurance and other staff in the planning and purchasing departments if required.
- Write and conduct process validation protocols and reports when required.
- Conduct risk assessment analysis for formulation impacted changes
- Initiate change controls and deviations when required
- Coordinate with QC regarding stability studies and assist in internal and external audits
