Position Summary:

Associate Scientist position in a growing team that supports a variety of analytical testing in support of the manufacturing of biopharmaceutical products in a contract development and manufacturing space.  

Position Responsibilities:

• Support in-process testing in support of the manufacturing of biopharmaceutical products

• Perform cGMP testing on product release and stability programs. Perform stability trending, provides support for troubleshooting and laboratory investigations.

• Regularly exercises technical discretion in the execution and interpretation of experiments that contribute to project goals. 

• Ensure accurate and complete documentation of results via electronic notebook, technical documents, power point, etc.

• Provide support for the review and approval of analytical test methods, study protocols and technical reports.

• Adheres to all safety requirements and assures that departmental employees comply with required safety procedures.

• Able to react to change productively and handle other essential tasks as assigned.

Minimum Requirements: 

• For Associate Scientist: Bachelor's degree in a related field and 5+ years’ experience or Master's degree with 3+ years' experience. 
• Experience with cGMP and biotechnology-derived product regulations a plus.
• Good written and verbal communication skills
• Good critical thinking and scientific skills, with a demonstrated ability to analyze, interpret, and clearly present complex data with conclusions.

Salary Range: $75,000 - $90,000

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, Sabbatical program, 401K matching with 100% vesting in 60 days and employee recognition programs.   

About KBI:

KBI Biopharma, Inc., a JSR Life Sciences company, is a global contract development and manufacturing organization (CDMO) providing fully integrated and accelerated drug development and biologics manufacturing services to life science companies. KBI supports its 500+ customers in advancing more than 160 drug candidates from preclinical and clinical stages to market, including the manufacture of ten commercial products. Recognized for quality manufacturing, KBI delivers robust process development and cGMP manufacturing services across its six global locations in the USA and Europe. For more information, visit www.kbibiopharma.com.

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.