Quality Assurance Specialist Role
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GMP Pharmaceuticals Group, a leading contract manufacturing company in Australia and New Zealand, is seeking an experienced Quality Assurance Specialist. The successful candidate will be responsible for maintaining compliance with relevant legislative standards and requirements.
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The role requires excellent critical thinking and problem-solving skills, as well as the ability to work independently and exercise effective time management.
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* Maintain and reinforce compliance with TGA, GMP, HACCP, NSW Food Authority, AQIS, and other legislative standards.
* Participate in the maintenance and renewal of appropriate licenses and perform general QA responsibilities.
* Regularly maintain and generate required documentations, reports, data, and records analyses for internal and external audits.
* Ensure compliance with SOPs, batch card, product's labelling and packaging material.
* Assist in conducting internal/external GMP audits to facilities and local suppliers.
* Investigate and identify quality issues, customer complaints. Raise corrective/preventative actions and closely monitor to ensure they are implemented effectively.
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Requirements
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* 1 year experience in similar roles, preferably in the Pharmaceutical industry.
* Science background, ideally in chemistry; however, biochemistry or chemical engineering will also be considered.
* In-depth knowledge of TGA, NSW Food Safety, HACCP, AQIS, GMP, and other relevant legislative requirements and best practices.
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Benefits
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* Able to think on their feet and demonstrate excellent critical thinking and problem-solving ability.
* Well-organized with great time management and attention to detail.
* Takes ownership of their own responsibilities.
* Can work independently and exercise effective time management to deliver results within agreed deadlines.
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About the Role
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* Valid driver's license and own transport.