Job Description

Activ Pharmaceuticals – Smeaton Grange NSW

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Activ Pharmaceuticals, based in Smeaton Grange, manufactures liquid and cream products in cosmetic and therapeutic grades and is a part of the Activ Pharmaceuticals Group.

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We are now looking to a Quality Control Chemist to join our dynamic team.

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Essential Criteria are as follows:

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- Minimum 3 years' experience working in a GLP/GMP Quality Control environment, with a strong understanding of the Code of GMP and its application within a laboratory setting.
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- Demonstrated experience performing analysis and formal release of starting materials, bulk products, and finished products in a timely manner.
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- Experience using pharmaceutical compendia such as BP, USP, and other relevant standards.
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- Minimum 3 years' hands‐on experience with GC, HPLC, IR, UV, and potentiometric analytical techniques, including troubleshooting and method optimisation.
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- Proven experience in analytical method validation in accordance with regulatory and industry requirements.
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- Experience performing laboratory equipment calibration, qualification, and ongoing performance verification activities.
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- Experience providing training and technical guidance on the operation, care, maintenance, and troubleshooting of HPLC, GC,



and other laboratory instruments.
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- Bachelor of Science (Chemistry) or a closely related scientific discipline.
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Duties of this position will include:

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- Performing OOS, OOT and OOE investigations and root cause analysis.
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- Providing technical support to Management (e.g., summarised QC data, trend records etc).
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- Providing analytical support to the product development department and stability program.
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- Maintenance of all QC records, including notebooks and equipment logbooks in accordance with GLP/GMP requirements.
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- Reviewing Supplier/Manufacturer CoAs, supply chain records and other QC documentation.
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- Performing reference solution standardisation.
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The successful candidate should also possess the following:

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- Ability to work independently or as part of a team.
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- Have a sound understanding of data integrity requirements in the laboratory.
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In return, Activ Pharmaceuticals will offer:

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- An immediate start working a 38-hour week with a 2.30pm finish on a Friday.
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- An equitable and ethical workplace.
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- The support of a skilled team working in a safe environment.
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📌 Quality Control Chemist TGA Facility (New South Wales)
🏢 Activ Pharmaceuticals
📍 New South Wales