Job summary
Job post source
This job is directly from KBI Biopharma
Job overview
The QC In-Process Support Associate at KBI Biopharma performs cGMP in-process analytical support with a focus on protein chemistry, contributing to drug substance testing and manufacturing operations.
Responsibilities and impact
The role involves executing analytical test methods like HPLC and UV-Vis, analyzing data, reviewing STAT samples, performing QC testing for release and in-process samples, maintaining documentation, troubleshooting, and adhering to safety protocols.
Compensation and benefits
The pay range is $19.23 to $26.44 per hour, with an annual bonus, medical, dental, vision coverage, paid PTO and holidays, 401K matching with immediate vesting, and employee recognition programs.
Experience and skills
Candidates need a BS in a scientific discipline or equivalent, with 0+ years of QC analysis experience in proteins, antibodies, peptides, or vaccines; cGMP experience is preferred along with strong communication skills.
Work environment and culture
KBI Biopharma values diversity and inclusion, promotes a safe and healthy workplace, and encourages innovation through diverse perspectives.
Company information
KBI Biopharma is a global CDMO under JSR Life Sciences, supporting over 500 customers with drug development and biologics manufacturing across six global locations, known for quality manufacturing and advancing over 160 drug candidates.
Unique job features
The position offers hands-on experience with bio-analytical techniques and contributes directly to manufacturing and quality control in a regulated cGMP environment.
Company overview
KBI Biopharma is a contract development and manufacturing organization (CDMO) that specializes in providing comprehensive biopharmaceutical services to biotechnology and pharmaceutical companies. They generate revenue by offering a range of services, including process development, clinical and commercial manufacturing, and analytical testing for biologics. Founded in 1996, KBI Biopharma has grown significantly, establishing multiple facilities in the United States and Europe. The company is known for its expertise in accelerating drug development timelines and ensuring high-quality production standards.
How to land this job
Position your resume to highlight your experience with cGMP in-process analytical support and your knowledge of protein chemistry, emphasizing techniques like HPLC, UV-Vis, and compendial testing.
Focus on showcasing your ability to perform detailed data analysis, troubleshooting, and documentation skills, including notebook and worksheet upkeep, which are crucial for this QC In-Process Support Associate role.
Apply through multiple platforms including KBI Biopharma's official corporate careers page and LinkedIn to maximize your application visibility and reach.
Connect with current employees in KBI Biopharma’s QC or analytical departments on LinkedIn; use ice breakers like commenting on recent company developments or asking about their experience with cGMP testing workflows to start conversations.
Optimize your resume for ATS by incorporating keywords from the job description such as 'cGMP', 'protein chemistry', 'HPLC', 'UV-Vis', 'data integrity review', and 'analytical test methods' to ensure your resume passes screening filters.
Utilize Jennie Johnson's Power Apply feature to automate tailored applications, identify multiple application channels, and find relevant LinkedIn contacts, allowing you to focus your time on preparing for interviews and networking effectively.
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