Quality Control Raw Material Analyst - Afternoon (New South Wales)

Quality Control Raw Material Analyst - Afternoon (New South Wales)

05 Aug
|
LIPA Pharmaceuticals
|
New South Wales

05 Aug

LIPA Pharmaceuticals

New South Wales

Quality Control Raw Material Analyst - AfternoonLipa Pharmaceuticals is Australia's leading manufacturer of complementary medicines, specialising in vitamins, pharmaceuticals, and health food supplements.
We have the capacity to produce a wide range of products including tablets, hard and soft capsules, liquids, powders, creams, gels, and probiotics.We are proud to have been recognised by Complementary Medicines Australia as the 'High-Quality Manufacturer of the Year' on nine occasions for the exceptional products we create.The OpportunityWe currently have a fantastic opportunity available for an experienced Quality Control – Raw Material Analyst to join our dedicated team on a permanent full time basis on Afternoon Shift (3pm-11pm).
The Quality Control – Raw Material Analyst plays a critical role in ensuring the quality, safety, and compliance of raw materials used in the production of our products.
This position involves conducting analytical testing, documentation and compliance checks to meet industry and regulatory standards.What we offerImmediate start with onsite car parkingWork with a results-driven and passionate teamOngoing training and supportGuidance by a supportive management team with a clear visionEmployee advantages, including a Rewards and Recognition ProgramResponsibilitiesConduct physical and chemical testing of raw materials, ensuring compliance with specifications and regulatory requirementsPerform identification, purity, and potency tests using analytical techniques such as HPLC, GC, FTIR, UV-Vis Spectroscopy,



and titrationsPrepare and standardise reagents and solutions for laboratory testingReview and compare results against approved specificationsDocument all testing procedures and results accurately in accordance with TGA requirementsMaintain laboratory equipment by performing routine calibrations, troubleshooting, and liaising with service engineers when neededTertiary qualification in Chemistry, Pharmaceutical Science, or a related disciplineExperience in a quality control laboratory within the complementary medicine or pharmaceutical industryHands-on experience with analytical instrumentation and techniquesStrong knowledge of pharmaceutical testing and regulatory requirementsHigh attention to detail with excellent problem-solving skillsAbility to work under tight deadlines while maintaining accuracy and complianceStrong communication and teamwork skillsPlease Note:Lipa Pharmaceuticals has a strong commitment to health and safety, with a pre-employment medical requiring successful completion, prior to an offer being made.
We do not accept unsolicited applications from third parties.
Applicants must be eligible to work in Australia.
Additionally, as our facility is not accessible by public transport you will need your own transportation to get to work.Lipa Pharmaceuticals is an Equal Employment Opportunity (EEO) employer.
We are committed to providing a diverse and inclusive work environment for all employees and applicants, regardless of race, colour, nationality, gender, age, disability, religion, sexual orientation, gender identity, or any other characteristic protected by law.
We encourage individuals from all backgrounds to apply'
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📌 Quality Control Raw Material Analyst - Afternoon (New South Wales)
🏢 LIPA Pharmaceuticals
📍 New South Wales

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