Biopharmaceutical Scientist II
4 weeks ago
About the Role
We are seeking a highly motivated and driven individual to join our team as an MBP Scientist II in Brisbane, Australia. This role is targeted towards an early career graduate with a biotech or a science degree, and complete unit operations in media and buffer preparation suites as advised by the MBP Supervisor.
Key Responsibilities
- Provide meaningful accountability to the overall departmental responsibility for the production of biopharmaceutical solutions and process intermediates, including maintaining optimized operational areas. Dispense raw materials, prepare media and buffer solutions (multiple 1000 L batches per day), manifold preparation and autoclaving, filter integrity testing.
- Work proactively to supply lead lean (OE) initiatives and continuous improvements. Revise, assist in review, and write documentation such as SOPs and ACFs.
- Perform equipment testing, troubleshooting, and complete validation protocols with developed skills of Bioprocess Scientist II. Support the implementation of new procedures and/or equipment in the OPS department in consultation with other owners and users, including support to changes (CRF).
- Propose and implement Corrective and Preventive Actions and support the timely closure of Deviation Reports and Change Controls as well as writing Minor Deviation Reports.
- A pro-active demeanor and personal initiative are encouraged to identify and overcome practical problems, propose possible solutions, and communicate to the responsible person.
- Communicate with suppliers about issues of technical nature.
- All activities should be performed independently within the department, coherent with cGMP Quality System and the Patheon EH&S requirements.
- Any reasonable additional tasks that might be required for day-to-day operational activities.
Requirements and Qualifications
- Tertiary education in science or engineering-based field (i.e. biopharmaceutical manufacture, biotechnology, process technology) or relevant proven experience.
- Very good knowledge and working in cGMP environment.
- Specific knowledge of relevant process unit operations and quality systems.
- Strong organizational, scheduling, and planning skills.
- Ability to work unsupervised.
- Good communication, flexibility, reliability, and assertiveness.
- Responsible and proactive.
- Enforce OHS policies and procedures and ensure a safe and balanced workplace environment.
- Enforce the Chain of Responsibility obligations under the Australian Heavy Vehicle National Law.
- Your position may require you to participate in on-call work. If you are on call, you are required to be available for immediate return to work outside of your normal and regular work pattern. Should this be a requirement of your position, you will be remunerated per the Company's policy.
About Us
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $44 billion. Our Mission is to enable our customers to make the world Healthier, cleaner, and Safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies, or increasing efficiency in their laboratories, we are here to support them. Our team of more than 125,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience, and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD. For more information, please visit www.thermofisher.com.
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