Sample Coordinator II-Analytical Development
Job Location:
Durham, NC - USA
Monthly Salary:
Posted on:
Vacancies:
Job Summary
Position Summary:
Perform the day-to-day management and distribution of samples. This person is responsible for:
Receipt and login of submitted samples.
Receipt and login of in-process samples and final product.
Storage inventory and maintenance of retention samples.
Ensures time sensitive samples are received and communicated to the testing teams by Sample Coordination prior to expiration (work assigned overtime and off-shift hours if necessary)
Storage inventory maintenance and issuance of reference standards used in testing.
Interacts with LIMS system as applicable.
Ships samples to contract facilities.
Maintains and monitors sample storage equipment (controlled temperature units CTUs) such as refrigerators freezers etc.
Issues controlled data forms (or equivalent electronic notebook)
Additional Responsibilities:
Logs in all samples and materials submitted and maintains inventory (including communication to testing teams)
Shipping samples as needed
Issuance of controlled data forms
Maintain and monitor of sample storage equipment
Assists with writing and submitting weekly Rees (or equivalent monitoring system) reports and acts as contact for monitoring system during business hours.
Acts as Qualified Trainer (if applicable) for Sample Coordination procedures; is SME on sample management processes.
Assists in investigation and resolution of excursions or other deviations.
Consistently resolves sample submission errors independently.
Stages stability studies according to the client approved protocols.
Performs stability pulls for time point testing
Helps maintain the workspace by entering any work requests as needed
Minimum Requirements:
HS and 6 years AS/AA and 3 years or Bachelors and 1 years of industry or lab experience or equivalent. Previous experience in sample management or work in cGMP environment preferred.
Salary Range: $26.95/hr.- $32.36/hr.
Salary range provided per current averages and expectations. The salary and job title for this opening will be based on the selected candidates qualifications and experience and may be outside this range. KBI has a robust total rewards strategy which includes an annual bonus structure for all employees medical dental and vision coverage paid PTO and holidays 401K matching with 100% vesting in 60 days and employee recognition programs.
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.
Required Experience:
IC
About Company
KBI Biopharma Inc. is a global contract development and manufacturing organization (CDMO / CMO) offering Cell Line Development, Process Analytical & Formulation Development, Clinical & Commercial Manufacturing, and more.
