6 days ago , from Thermo Fisher Scientific
Work Schedule
12 hr shift/daysEnvironmental Conditions
Able to lift 40 lbs. without assistance, 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 shiftJob 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!
Job Title: DSP Bioprocess Scientist III
Reports to: DSP Supervisor
Key Responsibilities: Fully trained and independently complete 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 DSP Senior Bioprocess Scientist. Support and implement new procedures and/or equipment in the OPS department in consultation with other owners and users. Revise and author batch records, SOPs and logbooks.Complete validation protocols for which a DSP Bioprocess Scientist skill is required. Adhere to Patheon cGMP Quality Management System and the Patheon EH&S requirements. Being the lead investigator for minor and major deviation, and propose and implement corrective and preventive actions, as well as ensure 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
Tertiary education in science or engineering based field (i.e. biopharmaceuticals manufacture, biotechnology, process technology). Very good knowledge in cGMP environment. Specific knowledge of downstream processing such as chromatography protein purification, virus inactivation, virus filtration, ultrafiltration and diafiltration, and formulation.
Skills & Attributes
Ability to work unsupervised. Good communication, flexibility, reliability and assertiveness. Responsible and proactive.
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