Job Summary:
Responsible for supporting product characterization studies of biopharmaceutical products through performing protein mass spectrometry and biochemical techniques. Preference on previous mass spectrometry experience and routinely use that expertise to advance client programs efficiently and effectively. Additional need for good communication with clients and internal groups. Adaptability to adjust to program priorities to meet timelines. Approximately 75% of time planning, executing, reviewing, and documenting client work.
Required Competencies:
- Educational Background Sci-I: Bachelor’s degree in science and 7 years of related experience; Master’s degree and 5 years of related experience; Ph. D. in a scientific discipline.
- Scientific Knowledge: Perform testing on biotherapeutic samples using mass spectrometry and biochemical techniques, such as HPLC and CE.
- Scientific Knowledge: Perform peer review of data and reports associated with the development and qualification of analytical methods and the testing of in‑process and drug substance/drug product samples.
- Technical Writing: Produce high-quality documentation suitable for publication and regulatory requirements.
- Communication: Possesses good written and verbal communication skills. Advise management of work status. Interact positively and productively with clients.
- Self-Motivation: Ability to work with minimal supervision and a desire to take on additional responsibilities as they arise.
- Active Learner: Ability to learn new processes and procedures and adjust to fluctuations in workload. Seeks out opportunities to learn new information and improve processes.
- Collaboration: Ability to work with multiple teams to meet client needs in a dynamic environment.
- Organization: Ability to maintain organization of space, documentation, and materials to ensure smooth workflow and tracking.
- Detail-Oriented: Great attention to detail in a multitasking environment to ensure accuracy.
- Safety: Adhere to all safety requirements and assure that departmental employees comply with required safety procedures.
Preferred Competencies:
- Technological Knowledge: Previous experience with mass spectrometry for peptide mapping, intact mass, and glycan characterization. Previous experience with Thermo Scientific Orbitrap and Agilent TOF/Q-TOF instrumentation is a bonus.
- Technological Knowledge: Previous experience with any of the following techniques/instrumentation – HPLC, capillary electrophoresis, capillary isoelectric focusing.
- Technological Knowledge: Previous experience with technical writing.
Salary Range: $85,000 - $110,000
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, Sabbatical program, 401K matching with 100% vesting in 60 days and employee recognition programs.
KBI Biopharma is committed to providing a safe and healthy workplace. Any employee entering a KBI site located in the US must inform KBI Biopharma of their vaccination status and must submit their vaccination status. All vaccinated employees are required to provide proof of their COVID-19 vaccination, with a COVID-19 vaccination which has been granted FDA approval or Emergency Use Authorization.
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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What We Do
KBI Biopharma is an award-winning biopharmaceutical contract services organization providing fully-integrated, accelerated drug development and biomanufacturing services to pharmaceutical and biotechnology companies globally.
With each of our 500+ client partners, we have worked closely to personalize and rapidly accelerate their drug development programs. Built upon a foundation of world-class analytical capabilities, we deliver efficient process development and clinical and commercial cGMP manufacturing services for mammalian, microbial, and cell therapy programs.
KBI is proud to be a JSR Life Sciences Company.