QC Scientist - 40120
QC Scientist - 40120
- 1 Vacancy
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Job Description
Benefits Competitive salary package Work with a globally recognised biotechnology leader known for scientific excellence and patient impact About the Company This global biopharmaceutical organisati...
- Competitive salary package
- Work with a globally recognised biotechnology leader known for scientific excellence and patient impact
This global biopharmaceutical organisation is dedicated to developing and delivering innovative therapies that improve the quality of life for people with rare and serious diseases.
About the OpportunityThe QC Analytical Technology Scientist plays a pivotal role within the Quality Control Analytical Technology (QCAT) team, driving analytical innovation and method lifecycle management. This position is responsible for planning and delivering projects and investigations, supporting analytical method development, validation, and transfer. Working collaboratively within a high-performing technical team, this role supports the integration of new technologies and ensures compliance with cGMP standards to maintain product quality and regulatory alignment.
Duties- Develop, plan, and execute analytical studies and investigations aligned with QCAT objectives
- Prepare and review SOPs, test procedures, protocols, and study documentation
- Conduct method development, qualification, validation, and transfer between QC, R&D, and external partners
- Ensure adherence to cGMP, data integrity, and quality documentation standards
- Participate in audits, inspections, and regulatory submissions as required
- Support maintenance and calibration of QC laboratory instrumentation
- Provide technical assistance, training, and mentorship to colleagues
- Actively contribute to safety investigations, improvements, and innovation initiatives
- Bachelor's degree in Engineering, Physical, or Biological Sciences (postgraduate qualification desirable)
- Minimum 3 years' experience in cGMP Quality Control or at least 1 year in analytical method development for biological products
- Proven experience in analytical method development, validation, or transfer
- Understanding of analytical method lifecycle management and cGMP principles
- Strong problem-solving and data interpretation skills
- Excellent communication, documentation, and teamwork capabilities
- Experience with LIMS and quality management systems advantageous
You'll join a collaborative, safety-focused environment where scientific curiosity and continuous improvement are encouraged. The team values integrity, innovation, and high performance, fostering an inclusive and supportive culture that promotes personal and professional development.
How to ApplyClick apply or contact Georgia Graham - Senior Recruitment Consultant at for a confidential discussion.
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