QC Analyst II

jsrglobal· KBI Biopharma, Inc.
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Full timeKBI Biopharma, Inc.

About this role

At KBI Biopharma, we are advancing science and accelerating breakthroughs. As a global leader in biopharmaceutical development and manufacturing, we empower life science companies to bring new medicines and vaccines to the world faster. Explore your potential at KBI, where innovation meets impact. 

 

Position Summary:

This role is responsible for analytical testing and laboratory support in a contract manufacturing facility. 

 

Position Responsibilities:

  • Product Testing: In-process and release testing as assigned; techniques include (but not limited to) HPLC, SDS-CGE, ELISA, qPCR, SoloVPE, and compendial testing per USP
  • Solution preparation
  • Analysis and collation of data to draw conclusions
  • Trend analysis using control charting
  • Execution of method transfer, method qualification, and/or method validation testing under protocol
  • Supports lab investigation and deviation reports
  • Supports implementation of Corrective and Preventive Actions
  • Tracks department metrics upon request; actively engages in improvement of department metrics
  • Ensures state of safety and regulatory audit readiness at all times
  • Participates in data review activities, as needed
  • Ensures Trainer qualification status to expand team matrix
  • Laboratory support
  • It is the expectation that this position is required to be onsite full time with a minimum of 75% of time in the laboratory/facility

 

Minimum Requirements:

  • QC Analyst I requires Bachelor’s degree in chemistry, biochemistry or related area (or equivalent training) with 0+ years’ experience. QC Analyst II requires Bachelor’s degree as described and 2+ years’ experience or Master’s Degree with 0+ years’ experience. Senior QC Analyst requires Bachelor’ degree as described and 4+ years’ experience or Master’s Degree with 2+ years experience.
  • Strong ELISA and other plate-based assays experience preferred
  • Experience in QC analysis of proteins, antibodies, peptides, or vaccines a plus, but not required
  • Excellent verbal and written communication skills
  • Experience working in a cGMP environment preferred

 

About KBI: 

KBI Biopharma, Inc., a JSR Life Sciences company, is a global contract development and manufacturing organization (CDMO) providing fully integrated and accelerated drug development and biologics manufacturing services to life science companies. KBI supports its 500+ customers in advancing more than 160 drug candidates from preclinical and clinical stages to market, including the manufacture of ten commercial products. Recognized for quality manufacturing, KBI delivers robust process development and cGMP manufacturing services across its six global locations in the USA and Europe. For more information, visit www.kbibiopharma.com.


KBI is a proud EEO/AA employer dedicated to building a diverse and inclusive workforce. We believe that innovation thrives in an environment where all voices are heard and valued. That's why we actively seek individuals from all backgrounds – regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability, or veteran status – and strongly encourage all qualified candidates to apply and bring their unique perspectives to our team.

KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. 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.

I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.

I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

Frequently Asked Questions

Is the salary disclosed for the QC Analyst II position at jsrglobal?
The salary for this QC Analyst II role at jsrglobal is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the QC Analyst II position at jsrglobal located?
This QC Analyst II role at jsrglobal is based in 2 Locations, USA - NC - Durham - Hamlin Rd, USA - NC - Durham - National Way. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the QC Analyst II role at jsrglobal full-time or part-time?
This is listed as a Full time position. It is posted as a QC Analyst II role in the KBI Biopharma, Inc. department at jsrglobal.
Which team or department does the QC Analyst II at jsrglobal belong to?
This QC Analyst II position is part of the KBI Biopharma, Inc. department at jsrglobal. See the full job description for more information about the team structure and responsibilities.
How do I apply for the QC Analyst II position at jsrglobal?
Click the "Apply Now" button on this page. You will be redirected to jsrglobal's official application portal hosted on workday where you can submit your application directly.
QC Analyst II
jsrglobal
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