Engineer 1/2
KBI Biopharma
Engineer 1/2
KBI Biopharma
CDMO delivering cell line development
This role offers an exciting opportunity for an entry level engineer to impact efficiency, quality, and innovation within biologics processing at a KBI Biopharma. As an MS&T Engineer, you will be pivotal in supporting cGMP production operations through application of engineering principles to technology transfer, existing manufacturing processes, and process validation. This role offers opportunities for hands-on development of biologics manufacturing knowledge, skills, and expertise. Working closely with cross-functional teams and directly engaging with clients, you will support the introduction of manufacturing processes at production scale, identify and implement process improvements, troubleshoot technical issues, and ensure that client and regulatory standards are consistently met.
This position is ideal for an engineer with a background in chemical and biological engineering, who thrives in a collaborative environment and is committed to driving excellence in manufacturing science and technology. This role offers opportunities for professional growth, exposure to cutting-edge technologies, and a dynamic work environment where your contributions will directly influence production success and client satisfaction. This role applies engineering skills to process engineering projects in support of process development, process transfer, and clinical/commercial manufacturing.
Responsibilities:
Knowledge, Skills, Abilities
Salary Range:
Engineer I: $63,000 – $86,900
Engineer II: $74,000 – $102,300
Salary range provided per current averages and expectations. The salary and job title for this opening will be based on the selected candidate’s qualifications and experience and may be outside this range. KBI has a robust total rewards strategy which includes an annual bonus structure for all employees, medical, dental, and vision coverage, paid PTO and holidays, 401K matching with 100% vesting in 60 days and employee recognition programs.
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.
CDMO delivering cell line development
KBI Biopharma is a CDMO that accelerates the development of biological medicines by providing rapid cell line generation and process development for preclinical programs. It uses established mammalian and microbial expression systems (such as CHO K1, CHO S, CHO DG44, HEK293, and DXB11 E. coli) to create production cell lines and develop integrated manufacturing processes. Compared with competitors, it wins on speed, end-to-end capability, and flexibility across multiple platforms to move projects quickly from discovery to preclinical milestones for a diverse client base. Its goal is to reduce risk, shorten development timelines, and expand global access to life-saving biologic therapies.
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