Benefits
* Work with one of the world's most respected biopharma organisations
* Join a high-calibre scientific team working on impactful therapeutic products
* Gain exposure to innovativeQC Chemistry techniques
* Standard Monday to Friday hours
* Collaborative team of specialists and career-enhancing experience in GMP
About the company
Work within a large global Biotechnology company that boasts a good company culture that is always expanding.With state-of-the-art laboratories, you'll join a passionate team dedicated to maintaining the highest standards of quality, safety, and regulatory compliance.
About the Opportunity
We're seeking a dedicated Quality Control Chemist to perform crucial analytical testing activities, ensuring the ongoing safety and quality ofthe organisations life-saving products. This role provides you with the opportunity to utilize your technical expertise within a high-performing team and significantly contribute to public health.
Responsibilities:
* Conduct routine laboratory testing of products including raw materials and finished goods.
* Perform wet chemistry techniques, titration, pH, conductivity testing, HPLC, GC-MS, and other analytical methods.
* Ensure precise sampling, analysis, and accurate logging into Laboratory Information Management Systems (LIMS).
* Adhere strictly to Good Manufacturing Practice (GMP) and internal data integrity standards.
* Conduct equipment calibration, validation, and preventive maintenance activities.
* Participate in out-of-specification investigations and support resolution activities.
* Assist with laboratory documentation, protocols, and SOP updates to maintain regulatory compliance.
Requirements:
* Tertiary qualification in Chemistry, Biochemistry, Pharmaceutical Science, or related discipline.
* Demonstrated laboratory experience, ideally in pharmaceuticals or biotech sectors.
* Proven proficiency in analytical methods such as HPLC, GC-MS, titration, wet chemistry, and physical testing techniques.
* Familiarity with LIMS and other electronic quality management platforms.
* Sound knowledge and experience with GMP, GLP, and regulatory compliance standards.
* Excellent attention to detail, analytical thinking, and problem-solving abilities.
* Strong written and verbal communication skills.
* Ability to work effectively in a team and independently manage tasks to deadlines.
Culture
You'll be joining a friendly team of 8-14 within a large, mission-driven organisation where scientific excellence, integrity, and collaboration are core values. The team encourages autonomy, proactive problem-solving, and mutual support, with access to world-class systems and technology.
Why this opportunity is right for you
This is a Full-time 5-month contract opportunity based in Melbourne working onsite Monday to Friday.
How to Apply
Click apply or contact Georgia, SeniorRecruitment Consultant on+61370371653for a confidential discussion.
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