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 innovative QC 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 of the 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, Senior Recruitment Consultant on +61370371653 for a confidential discussion.