KBI
KBI: US - Downstream Process Development Scientist II
USA - CO - Boulder · Mid
Sponsorship not specified$106k-$146kDetected 30 days ago
Customer SupportGMPCommunication
About the role
- The PD Scientist II is responsible for maintaining training compliance, according to site expectations.
Responsibilities
- Works toward developing a broad knowledge of state-of-the-art principles and theory.
- Supports downstream process development efforts in the laboratory and manufacturing areas.
- Will lead the downstream portion of development, process characterization, and/or technology transfer programs, acting as subject matter expert (SME), and directing the efforts of the team in meeting the project deliverables.
- Responsible for developing/maintaining a current understanding of cGMP and other regulatory requirements.
- Conceptualizes, proposes and executes the evaluation, development and implementation of new downstream technologies leading to process improvements and efficiency of operation in support of downstream process development and manufacturing activities.
- Documents procedures, observations, and results in laboratory notebooks and responsible for maintaining training compliance, according to site expectation. Reviews documentation and records as assigned.
- The Downstream Process Development (PD) Scientist II provides process development ownership for a product, including all development and design decisions, with some oversight and supervision from senior process development staff.
- 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.
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 discipline.
- Adheres to all safety requirements and assures that departmental employees comply with required safety procedures.
Nice to have
- Experience with downstream process development and chromatography equipment required.
- Excellent written and verbal communication skills, focus on customer service, and ability to meet strict client deadlines.
- Highly collaborative.
- Knowledge of GMPs and biotechnology-derived product regulations preferred.
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.