Posted 23 days ago
Process Development Data Reviewer/ Senior Research Associate
AI Summary
Reviews process development data for contract services projects involving monoclonal antibodies, recombinant proteins, peptides, and other biologics, verifying calculations and documentation for accuracy and compliance.
About this role
NAME OF EMPLOYER: KBI Biopharma, Inc.
POSITION TITLE: Process Development Data Reviewer/ Senior Research Associate
POSITION LOCATION: 4117 Emperor Blvd, Durham, NC 27703
HOURS: Full Time/40 hours
JOB DUTIES: Perform data review for contract services projects, including process development programs, process characterization projects and material supply campaigns for monoclonal antibodies, recombinant proteins, peptides and other biologics. This review includes the verification that calculations and documented information are correct, complete, and accurate in accordance with guidance documents and internal procedures. Make detailed observations and report documentation corrections to the relevant personnel, as needed. Perform timely and critical review of process development data to ensure all data, calculations, and documented information are present, complete, accurate, and compliant. Add comments and edits to applicable documents to identify incomplete/inaccurate data and other errors. Route documents for additional review and corrections as needed. Ensure corrections are completed accurately.
REQUIREMENTS: Bachelor’s degree or equivalent in Biotechnology, or related field of study and 4 years of experience with lab execution, data verification in the biotechnology industry, or any combination thereof. Employer will accept a Master’s degree or equivalent in Biotechnology or related field of study and 2 years of lab execution, data verification in the biotechnology industry, or any combination thereof, in lieu of Bachelor’s degree or equivalent and 4 years of experience.
Applicants must have demonstrated experience with:
1) Reviewing transcription of raw data into records and final reports, including data transformed by manual calculations.
2) Data analysis using statistical software.
3) GDP, GMP, and biotechnology-derived product regulations.
4) Communicating and discussing review results in a non-technical language with document stakeholders.
5) Electronic document management systems.
6) Laboratory notebooks and batch records.
CONTACT: If interested please apply online at https://www.kbibiopharma.com/careers with R00008788.
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.
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.
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