Process Development Data Reviewer/ Senior Research Associate

Posted 12 Days Ago
Be an Early Applicant
Durham, NC, USA
In-Office
Senior level
Biotech
The Role
Review process development and biopharmaceutical project data for accuracy, completeness, compliance, and proper documentation. Verify calculations, transcription of raw data, laboratory records, batch records, and final reports. Identify errors, add comments and edits, communicate corrections to stakeholders, route documents for further review, and confirm corrections are completed accurately. Projects involve monoclonal antibodies, recombinant proteins, peptides, and other biologics.
Summary Generated by Built In

NAME OF EMPLOYER: KBI Biopharma, Inc. 

POSITION TITLE: Process Development Data Reviewer/ Senior Research Associate 

POSITION LOCATION: 4117 Emperor Blvd, Durham, NC 27703  

HOURS: Full Time/40 hours 

 

JOB DUTIES: Perform data review for contract services projects, including process development programs, process characterization projects and material supply campaigns for monoclonal antibodies, recombinant proteins, peptides and other biologics. This review includes the verification that calculations and documented information are correct, complete, and accurate in accordance with guidance documents and internal procedures. Make detailed observations and report documentation corrections to the relevant personnel, as needed. Perform timely and critical review of process development data to ensure all data, calculations, and documented information are present, complete, accurate, and compliant. Add comments and edits to applicable documents to identify incomplete/inaccurate data and other errors. Route documents for additional review and corrections as needed. Ensure corrections are completed accurately. 

       

REQUIREMENTS: Bachelor’s degree or equivalent in Biotechnology, or related field of study and 4 years of experience with lab execution, data verification in the biotechnology industry, or any combination thereof. Employer will accept a Master’s degree or equivalent in Biotechnology or related field of study and 2 years of lab execution, data verification in the biotechnology industry, or any combination thereof, in lieu of Bachelor’s degree or equivalent and 4 years of experience.

Applicants must have demonstrated experience with: 

1) Reviewing transcription of raw data into records and final reports, including data transformed by manual calculations.  

2) Data analysis using statistical software.  

3) GDP, GMP, and biotechnology-derived product regulations.  

4) Communicating and discussing review results in a non-technical language with document stakeholders.  

5) Electronic document management systems.  

6) Laboratory notebooks and batch records. 

CONTACT: If interested please apply online at https://www.kbibiopharma.com/careers with R00008788.

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.  

 

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 or equivalent in Biotechnology or a related field, plus 4 years of experience with lab execution, biotechnology data verification, or a combination thereof.
  • Master's degree or equivalent in Biotechnology or a related field, plus 2 years of experience with lab execution, biotechnology data verification, or a combination thereof, may substitute for the bachelor's degree and four years of experience.
  • Experience reviewing transcription of raw data into records and final reports, including manually calculated data.
  • Experience performing data analysis using statistical software.
  • Experience with GDP, GMP, and biotechnology-derived product regulations.
  • Experience communicating review results in non-technical language with document stakeholders.
  • Experience with electronic document management systems.
  • Experience with laboratory notebooks and batch records.

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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