KBI
KBI: US - Process Development Scientist II
USA - CO - Boulder · Mid
Sponsorship not specified$106k-$146kDetected 30 days ago
ReactCustomer SupportGMPLeadership
About the role
- Additionally, the PD Scientist II may mentor and train junior staff within the process development group including co-ownership of programs as needed.
- The PD Scientist II is responsible for maintaining training compliance, according to site expectations.
- Executes process development, process characterization, and technology transfer of microbial upstream/downstream processes to commercial cGMP facility.
Responsibilities
- Supports process development efforts in the laboratory and manufacturing areas. Executes experiments with some oversight. Conceptualizes and proposes process development and manufacturing based on process data.
- Works toward developing a broad knowledge of state-of-the-art principles and theory; provides some technical leadership within the group.
- Will lead the upstream portion of development, process characterization, and/or technology transfer programs, acting as subject matter expert, and directing the efforts of the team in meeting the project deliverables.
- Coach and develop departmental scientists. Assist in guiding the professional growth of team.
- Responsible for developing/maintaining a current understanding of cGMP and other regulatory requirements.
- The PD Scientist II provides process development ownership for a product, including all development and design decisions, with some oversight and supervision.
- They can apply advanced scientific principles to design and execute laboratory studies for unit operation development and optimization and solve problems of increasing scope and complexity.
- This workflow encompasses process development scope as well as support of technology transfer activities in preparation for cGMP production.
- Technical expertise is developing in one or more areas of the job function and may be called upon to support troubleshooting or other activities beyond an individual program scope.
Requirements
- B.S. degree and a minimum of 6+ years of related experience
- M.S. and 4+ years of related experience or Ph.D. and 1+ years related experience in a scientific
- Adheres to all safety requirements and assures that departmental employees comply with required safety procedures.
Compensation
- $106,480-$146,410
Benefits
- Provide technical support for cGMP manufacturing through floor coverage, batch document review, and support of deviations and change controls with some oversight.
- 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.
Equal opportunity
- KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force.
This listing is sourced directly from KBI's careers page and normalized into a canonical job model.