Associate Scientist / Scientist I - AFS
KBI Biopharma
Summary
Associate Scientist/Scientist I 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.
Job description
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.
Requirements
- For Associate Scientist: Bachelor's degree in a related field and 5+ years' experience or Master's degree with 3+ years' experience.
- For Scientist I: Bachelor's degree in a related field and 6+ years' experience or Master's degree and 5+ years' experience or PhD and 0+ 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.
Benefits
- Annual bonus structure
- Medical, Dental & Vision
- Paid PTO
- Paid holidays
- 401(k) Matching
- Employee recognition programs
Company overview
KBI Biopharma is an award-winning global contract development and manufacturing organization (CDMO) that provides fully integrated, accelerated drug development and biologics manufacturing services to pharmaceutical and biotechnology companies worldwide. Founded in 1996 and now part of JSR Life Sciences, KBI has established itself as a next-generation CDMO specializing in complex biologics. The company serves over 500 client partners and has supported the advancement of more than 160 drug candidates from preclinical stages to market, including the manufacture of ten commercial products. KBI's comprehensive service portfolio includes cell line development, process development, analytical services, formulation development, and clinical and commercial cGMP manufacturing for both mammalian and microbial programs. With strategically located facilities across the United States and Europe, KBI leverages world-class analytical capabilities and proprietary platforms like SUREtechnology™ and PUREplatform™ to deliver personalized, accelerated solutions for biopharmaceutical development. The company is recognized for its scientific excellence, quality manufacturing, and commitment to helping clients bring innovative medicines to patients faster.