QA Specialist II

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:

• BS and 11 years experience or MS and 8 years experience in a CGMP regulated
  environment within biopharmaceuticals or equivalent.
• Experience in QA review of analytical data (release in-process and stability) experience in reviewing method qualifications/validations and the review and approval of laboratory investigations and
  deviations. Knowledge of USP EU and JP cGMP guidelines.
• Ability to read analyze and interpret general business periodicals professional journals
  technical procedures or governmental regulations.
• Ability to write reports business correspondence and procedure manuals. Ability to effectively present information and respond to questions from groups of managers clients customers and the general public.
• Ability to solve practical problems and deal with a variety of concrete variables in
  situations where only limited standardization exists.
• Ability to interpret a variety of instructions furnished in written oral diagram or schedule form.
• Basic math skills are required.
• Ability to apply concepts of basic algebra and statistics.
• Be able to sit for long periods of time.
• Ability to lift 20 pounds.
• Ability to use word processing database spreadsheets power point internet e-mail calendar computer telephone

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.