Work Schedule
12 hr shift/days
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift
Job Description
At Thermo Fisher Scientific, each one of our 125,000 outstanding minds has a unique story to tell. Join us and contribute to our singular mission-enabling our customers to make the world healthier, cleaner and safer!
Becoming part of the team at Thermo Fisher Scientific, you'll do important work. Surrounded by collaborative colleagues, you'll have the support and opportunities that only a global leader can give. Our respected, growing organization has an outstanding strategy for the near term and beyond. Join our strong team, and help us make significant contributions to the world!
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Position Summary:
Manufacturing of biopharmaceutical products in compliance with international quality requirements as defined by TGA, FDA, EMEA, ICH, etc.
Key Responsibilities:
- Trained on and support execution of DSP unit operations (chromatography, virus inactivation, virus filtration, ultrafiltration-diafiltration and drug substance final fill) with the applicable production protocols and planning schedules, in a clean room environment under cGMP conditions.
- A pro-active attitude and personal initiative is encouraged to identify practical problems and communicates to the responsible person.
- Contribute in their DSP functions, such as maintaining production suite, supplies, equipment, logbooks, and data, as well as closing out batch record and material reconciliation in accordance with site SOPs and policies.
- Perform equipment maintenance and testing related to technical skills of Bioprocess Scientist DSP. Support and implement new procedures and/or equipment in the OPS department in consultation with other owners and users.
- Revise and author SOPs and logbooks.
- Adhere to Patheon cGMP Quality Management System and the Patheon EH&S requirements.
- Complete corrective and preventive actions, contribute in deviation investigations and support the timely closure of deviation reports and change controls.
- Implement lean (OE) initiatives and continuous improvements.
- Contribute to the transfer and understanding of specific new technologies to DSP.
- Connect with supplier about issued of technical nature.
Minimum Requirements/Qualifications:
Qualifications & Experience
Either experience in pharmaceutical industry OR tertiary education in science or engineering-based field (i.e. biopharmaceuticals manufacture, biotechnology, process technology).
Good understanding of cGMP practices.
Skills & Attributes
Ability to work unsupervised. Good communication, flexibility, reliability and assertiveness. Responsible and proactive.
Other Job Requirements:
Your position may require you to be on shift or on call. Should this be a requirement, there will be remuneration as per the Company's policy.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.