Job Summary:
Responsible for leading product characterization studies for biopharmaceutical products using protein mass spectrometry techniques to characterize primary structure, disulfide structure, and glycan content of products. Expert in mass spectrometry and routinely use that expertise to advance client programs efficiently and effectively. Additionally responsible for the leadership of multifaceted studies, including communication with clients, management of project timelines, and mentorship of lower-level staff. Approximately 75% of time planning, executing, reviewing, and documenting client work.
Required Competencies:
- Scientific Knowledge: Perform testing on biotherapeutic samples using mass spectrometry.
- 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.
- Leadership and Management: Direct internal/external project execution and ensure the procedure follows company, client, and relevant regulatory requirements.
- Leadership and Management: Manage cost and time constraints to meet committed targets and schedules.
- Leadership and Management: Responsible for training, mentoring, and/or management of lower-level associates.
- Technical Writing: Produce high-quality documentation suitable for publication and regulatory requirements.
- Communication: Possesses good written and verbal communication skills. Advise management of program status. Act as SME on programs and 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.
- Educational Background: Bachelor’s degree in science and 8+ years of related experience; Master’s degree and 6+ years of related experience; Ph. D. in a scientific discipline and 4+ years of related experience.
Preferred Competencies:
- Technological Knowledge: Previous experience with mass spectrometry methods including peptide mapping, intact mass, disulfide mapping, and glycan characterization.
- Technological Knowledge: Previous experience with any of the following techniques/instrumentation – HPLC, capillary electrophoresis, capillary isoelectric focusing, UV-Vis, biophysical techniques (SV-AUC, CD, DSC, FITR), particle techniques (DLS, MFI).
Salary: $118,000.00 - $162,800.00
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.