Process Development Associate I/II

Process Development Associate I/II Durham, NC Job Details Full-time $55,000 - $86,900 a year 1 day ago Qualifications Safe work practices Microsoft Word Biotechnology Statistics Computer operation Laboratory safety Report writing Microsoft Excel Microsoft Outlook Presentation software Laboratory equipment maintenance Customer service Technical documentation Project planning Labeling Bachelor of Science Laboratory experiments Maintenance work Process improvement Equipment troubleshooting Biotechnology GMP Mid-level Technical report writing Improving operational efficiency Master of Science Hazardous material storage Data entry Microsoft Teams Autoclave JMP Mammalian cell culture Bachelor's degree in biotechnology Research & development 2 years Hazardous waste disposal Communication skills Technical Proficiency Process engineering Statistical analysis tools

Full Job Description Job Summary:

The Upstream Process Development Associate participates in cell culture and harvest projects for mammalian cell lines in support of process development, scale-up, and technology transfer to cGMP manufacturing.

Primary Job Responsibilities:

Conducts laboratory experiments in support of upstream processes including the set-up, operation, and associated analysis of cell culture and bioreactor processes. This involves bioreactor preparation, autoclaving, inoculation, sampling, feeding, data entry, and data analysis for shake flask and various scale bioreactors (TubeSpins, Ambr15, Ambr250, 3 L & 15 L glass bioreactors, Wave, 50 L and 200 L Xcellerex single-use bioreactors). Performs calculations for growth data, specific productivity, bioreactor agitation and gassing scale up/scale down. Assist in data analysis using statistical software like Design Expert (DOE), JMP etc. Identifies and troubleshoots unexpected results with input and/or review from peers or management. Perform data entry and plotting, generate presentations, and support writing of technical reports. Maintain detailed electronic lab notebooks entries with shake flask and bioreactor test results following good documentation practices (GDP). Maintains a cell culture-specific project plan, including raw materials and equipment availability, in preparation of laboratory and pilot- scale runs. Support process transfer from process development to manufacturing. May contribute to the evaluation, development and implementation of new upstream technologies leading to process improvements and efficiency of operation in support of upstream process development and manufacturing activities. Contributes to general lab maintenance, equipment troubleshooting, and operational excellence initiatives in accordance with internal guidance. Assures proper labeling, handling, and storage of all chemicals used in the area; assures proper labeling and disposition of hazardous waste in satellite areas; adheres to all safety requirements and follows safe procedures, and attends all required safety and health training, including handling hazardous waste.

Minimum Requirements:

Process Development Associate I requires a B.S. degree in biotechnology. Process Development Associate II requires a B.S. degree and 2+ years experience or a M.S. degree. Excellent written and verbal communication skills, focus on customer service, and ability to meet strict client deadlines. Flexibility of hours to support upstream processes. Knowledge of GMPs and biotechnology-derived product regulations preferred. Experience in cell culture development, medium development or pilot-scale bioreactor operations is preferred. Experience using electronic lab notebooks and/or PI historian is a plus. Physical Demands Ability to lift up to 40-50 lbs, occasionally. Computer Skills MS Teams, Outlook, Word, Proficiency in Excel, and PowerPoint. Equipment Use Computer, telephone, lab equipment.

Salary:

Process Development Associate I:

$55,000-$75,900

Process Development Associate II:

$63,000-$86,900 KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply. I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary. I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.