Analytical Chemist - Quality Control

About AstraZeneca

AstraZeneca is a leading global biopharmaceutical company concentrating on the discovery, development, and commercialization of prescription medicines mainly in four therapy areas: Oncology; Cardiovascular, Renal and Metabolism (CVRM); Respiratory & Immunology (R&I); and Rare Disease.

The Sydney manufacturing facility at North Ryde is a prominent producer of high-quality medicines for Australia and global markets, recognized for its safety, efficient operations, and strong workplace culture within AstraZeneca's international network.

Role Overview

This full-time, six-month maximum term contract role based at North Ryde involves working within the collaborative Quality Control team to conduct GMP-compliant analytical testing on packaging materials, raw materials, and finished products using modern systems like Empower. The position emphasizes data integrity and audit preparedness while supporting manufacturing operations.

Key Responsibilities

• Conduct pharmacopoeia-based testing of raw materials.
• Perform HPLC analysis using Empower software, adhering to system suitability and method validation requirements.
• Produce and review thorough, compliant laboratory records that meet data integrity standards and are audit-ready.
• Manage Out-of-Specification (OOS) results and deviations including documentation, investigation support, and corrective actions in collaboration with Quality Assurance.
• Troubleshoot primary instrument and method issues with guidance from senior team members.
• Engage in Lean methodologies to enhance operational efficiency and workflows.
• Promote and uphold a strong Safety, Health & Environment culture, reporting observations when applicable.

Candidate Requirements

• Bachelor's degree in chemistry or a related scientific field.
• 2 to 4 years laboratory experience in a regulated or GMP environment preferred.
• Practical experience with HPLC, preferably with Empower software.
• Hands-on usage of GQC LIMS for sample and data management.
• Experience handling OOS outcomes including documentation and investigative support.
• Excellent documentation skills and a keen eye for detail along with clear verbal and written communication.
• Ability to work collaboratively and effectively manage time to meet testing deadlines.

Desirable Extras

• Knowledge or experience with systems such as 1Lab, SAP, and quality management tools (e.g., EQV) for handling deviations, CAPA, and change control.
• Exposure to audit processes within laboratory or manufacturing settings.
• Understanding of sterile manufacturing and stability program requirements.
• Interest in troubleshooting HPLC and raw material testing techniques.

Why Join AstraZeneca?

AstraZeneca fosters an empowering and inclusive culture that encourages scientific innovation and professional growth. Employees benefit from flexible working hours, supportive communities, and a commitment to diversity and lifelong learning.

Benefits

• Gain expertise on current software platforms including Empower, GQC LIMS, 1Lab, and SAP within GMP frameworks.
• Enhance your professional profile with practical experience in pharmaceutical Quality Control, audit preparation, and deviation management.
• Enjoy onsite perks such as free parking, subsidised canteen facilities, flexible start times, and additional leave days at North Ryde.

Recruitment Process

• Initial 30-minute interview via Teams or phone with recruitment to discuss your experience and answer preliminary queries.
• Comprehensive role-specific assessment at the Macquarie Park site including a values-based interview (approx 1 hour) and a pre-employment medical examination (up to 1.5 hours).
• Background verification involving references, identity proof, and a police check, required before an official offer.

Additional Information

AstraZeneca values diversity and inclusion, welcoming applications from candidates of all backgrounds and compliant with employment equity laws. Applicants requiring support for accessibility during recruitment may request accommodations. The application deadline is 25-July-2026.