Engineer I/II
KBI Biopharma
Summary
This role offers an exciting opportunity for an entry level engineer to impact efficiency, quality, and innovation within biologics processing at KBI Biopharma. As an MS&T Engineer, you will be pivotal in supporting cGMP production operations through application of engineering principles to technology transfer, existing manufacturing processes, and process validation. This role offers opportunities for hands-on development of biologics manufacturing knowledge, skills, and expertise. Working closely with cross-functional teams and directly engaging with clients, you will support the introduction of manufacturing processes at production scale, identify and implement process improvements, troubleshoot technical issues, and ensure that client and regulatory standards are consistently met.
Job description
This position is ideal for an engineer with a background in chemical and biological engineering, who thrives in a collaborative environment and is committed to driving excellence in manufacturing science and technology. This role offers opportunities for professional growth, exposure to cutting-edge technologies, and a dynamic work environment where your contributions will directly influence production success and client satisfaction. This role applies engineering skills to process engineering projects in support of process development, process transfer, and clinical/commercial manufacturing.
Responsibilities
- Provides engineering support during process development and tech transfer by evaluating and influencing process implementation strategies. Monitors process performance in manufacturing and lead process troubleshooting efforts. Authors technical documents including product impact assessments, product campaign summaries and/or CPV reports.
- Established expertise in biotech unit operations. Ability to apply engineering skills to solve problems of moderate scope and the ability to determine when additional technical resources are required. Strong technical writing and communication skills.
- Works based on general guidance from a supervisor to resolve technical problems of moderate scope and complexity. Plans and conducts own work. Receives technical guidance for unusual or complex problems, supervisor approves proposed project plans.
- Sets priorities and leads initiatives and/or projects within function. Represents PD in providing technical solutions for specific projects.
Knowledge, Skills, Abilities
- ENG I: B.S. in Engineering or related field (ENG I)
- ENG II: M.S. in Engineering or related field, or B.S. and 3+ years relevant experience
Requirements
- B.S. in Engineering or related field (Engineer I)
- M.S. in Engineering or related field, or B.S. and 3+ years relevant experience (Engineer II)
- Established expertise in biotech unit operations
- Strong technical writing and communication skills
- Ability to apply engineering skills to solve problems of moderate scope
- Ability to determine when additional technical resources are required
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.