Qa analyst Jobs in Durham, NC
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Qa analyst • durham nc
QA Specialist II
KBI BiopharmaDurham, NC, United StatesQA Specialist
Accentuate StaffingDurham, NC, US- Promoted
Project Analyst
JLM Strategic Talent PartnersDurham, NC, USSr QA Analyst / Software
LCA Lab. Corp. of AmericaDurham NCQA Automation Engineer
Motion RecruitmentDurham, North Carolina, United StatesSenior QA Engineer
TaniumDurham, North Carolina, United StatesFinancial Analyst
JaggaerDurham, North Carolina, USA- Promoted
Financial Analyst
University of North CarolinaChapel Hill, NC, United States- Promoted
Finance Analyst
CiscoDurham, NC, United States- Promoted
Analyst, ALM
AmherstDurham, NC, US- Promoted
Manager II, QA
ThumbtackDurham, NC, USQuality Assurance (QA) Auditor
CSS, IncDurham, NC, USASupervisor – QA Incoming
Eli Lilly and CompanyDurham, North Carolina, United StatesQA Lead
Quanta part of QCS StaffingNorth Carolina- Promoted
Associate Director, QA Engineering - Combo Products
Iviva MedicalDurham, NC, USNCGrowth Analyst
UNC-Chapel HillChapel Hill, North Carolina, USAQA Clerk 815670
Alliance Industrial SolutionsDurham, NC, US- Promoted
Financial Analyst
Data SolutionsDurham, NC, US- Promoted
Accounting Analyst
FreudenbergDurham, NC, USQA Specialist II
KBI BiopharmaDurham, NC, United States- Full-time
JOB SUMMARY
This position is responsible for the compliance review of Biopharmaceutical
Development GMP data. This includes the review and approval of release, in-
process, and stability test data. This position is also responsible for the review and
approval of method qualifications and validations. Another responsibility is the
review and approval of laboratory investigations and deviations associated with the
biopharmaceutical development department.
JOB RESPONSIBILITIES :
- Performs compliance review on the following records : release, in-process, and stability data.
- Responsible for the review and approval of method qualifications and validations
- Responsible for the review and approval of deviations and laboratory investigations.
MINIMUM REQUIREMENTS :
environment within biopharmaceuticals or equivalent.
deviations. Knowledge of USP, EU and JP cGMP guidelines.
technical procedures, or governmental regulations.
situations where only limited standardization exists.
KBI Biopharma is committed to providing a safe and healthy workplace. Any employee entering a KBI site located in the US must inform KBI Biopharma of their vaccination status and must submit their vaccination status. All vaccinated employees are required to provide proof of their COVID-19 vaccination, with a COVID-19 vaccination which has been granted FDA approval or Emergency Use Authorization.
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.