QC Analyst II

Reposted 10 Days Ago
Be an Early Applicant
Durham, NC, USA
In-Office
Junior
Biotech
The Role
Perform analytical in-process and release testing (HPLC, SDS-CGE, ELISA, qPCR, SoloVPE, compendial USP), prepare solutions, analyze and trend data, support method transfers/qualifications/validations, investigations, CAPA, metrics, audit readiness, trainer qualification, and provide onsite laboratory support (≥75% onsite).
Summary Generated by Built In

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.

Skills Required

  • Bachelor's degree in chemistry, biochemistry, or related field (or equivalent training)
  • 2+ years' laboratory/QC experience (or Master's degree with 0+ years)
  • Excellent verbal and written communication skills
  • Onsite full-time presence with a minimum of 75% of time in the laboratory/facility
  • Strong ELISA and other plate-based assay experience
  • Experience in QC analysis of proteins, antibodies, peptides, or vaccines
  • Experience working in a cGMP environment

KBI Biopharma Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about KBI Biopharma and has not been reviewed or approved by KBI Biopharma.

  • Healthcare Strength Health coverage includes medical, dental, and vision with HSA/FSA options, alongside life and disability insurance. Employer-verified listings indicate solid foundational coverage across sites.
  • Leave & Time Off Breadth PTO and paid holidays are provided, with flexible or “unlimited” PTO available in some salaried roles and standard accrual with limited rollover elsewhere. This breadth supports time away options across job families.
  • Parental & Family Support Parental leave is available, with indications of 12 weeks for U.S. employees in recent materials. Maternity and paternity leave are included as part of the package.

KBI Biopharma Insights

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The Company
HQ: Durham, NC
1,282 Employees
Year Founded: 1996

What We Do

KBI Biopharma is an award-winning biopharmaceutical contract services organization providing fully-integrated, accelerated drug development and biomanufacturing services to pharmaceutical and biotechnology companies globally. With each of our 500+ client partners, we have worked closely to personalize and rapidly accelerate their drug development programs. Built upon a foundation of world-class analytical capabilities, we deliver efficient process development and clinical and commercial cGMP manufacturing services for mammalian, microbial, and cell therapy programs. KBI is proud to be a JSR Life Sciences Company.

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