In Process Research Associate

KBI Biopharma, Inc.; Durham (NC); On-site; USD 26,491 - 36,423; Full time

Benefits offered by this job

Annual bonus structure

Medical, dental, and vision coverage

Paid PTO and holidays

401(k) matching

Employee recognition programs

Job summary

KBI Biopharma, Inc. in Durham, NC is seeking an In-Process Support Associate to provide cGMP analytical support. The role involves performing testing using bio-analytical techniques like HPLC and analyzing data for drug substances manufactured internally.

The ideal candidate should possess a B.S. in a scientific discipline and excellent communication skills. Benefits include annual bonuses, medical coverage, and 401(k) matching.

Qualifications

• B.S. in a scientific discipline or equivalent experience.
• Experience in QC analysis of proteins, antibodies, peptides, or vaccines preferred.
• Excellent verbal and written communication skills.
• Experience working in a cGMP environment is preferred.

Responsibilities

• Perform testing on in-process or drug substances/products using bio-analytical techniques.
• Exercise technical discretion in design and execution of experiments.
• Make detailed observations and carry out elementary data analysis.
• Conduct troubleshooting analysis and maintain knowledge of instrumentation.
• Document work accurately and maintain familiarity with scientific literature.
• Ensure proper handling of chemicals and manage hazardous waste.

Skills

Protein chemistry background

Communication skills

Experience in QC analysis

cGMP environment experience

Education

B.S. in a scientific discipline or equivalent experience

Tools

HPLC

UV-Vis spectrophotometer

Job description

Position Summary

We are seeking an In-Process Support Associate with a strong protein chemistry background to provide cGMP in-process analytical support for drug substances manufactured internally. The Associate will be trained to execute analytical test methods and techniques, perform data analysis and integrity review of STAT samples, and occasionally conduct QC testing for release and in‑process samples.

Responsibilities

• Perform testing on in-process or drug substance/drug product using bio-analytical techniques such as HPLC, UV-Vis, and simple compendial testing.
• Exercise technical discretion in the design, execution, and interpretation of experiments to support project goals.
• Make detailed observations and carry out elementary data analysis.
• Conduct troubleshooting analysis and maintain knowledge of instrumentation.
• Document work in notebooks and worksheets accurately.
• Maintain familiarity with current scientific literature and professional expertise.
• Ensure proper labeling, handling, and storage of chemicals; manage hazardous waste disposition.
• Adhere to all safety requirements and attend required safety and health training.
• React to change productively and perform other essential tasks as assigned.

Requirements

• B.S. in a scientific discipline or equivalent experience.
• Experience in QC analysis of proteins, antibodies, peptides, or vaccines (preferred but not required).
• Excellent verbal and written communication skills.
• Experience working in a cGMP environment is preferred.

Pay Range

$19.23/hour – $26.44/hour

Benefits

Annual bonus structure; medical, dental, and vision coverage; paid PTO and holidays; 401(k) matching; employee recognition programs.

EEO and Diversity Statement

KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its workforce, welcoming candidates from all backgrounds.

About KBI

KBI Biopharma, Inc., a JSR Life Sciences company, is a global contract development and manufacturing organization (CDMO) that provides integrated drug development and biologics manufacturing services to life science companies.