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QC Analyst III 2013

QC Analyst III 2013

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Published by Bryan Nicoll
The position will include routine testing of in-process and final container samples for the release of avian vaccines. The individual will be responsible for ensuring all methods are performed as written and filed with regulatory agencies. The individual may conduct specific studies or projects to improve the quality or efficiency of the company’s products or procedures. The QC Analyst III will provide administrative and technical support in the absence of the QC Manager.
The position will include routine testing of in-process and final container samples for the release of avian vaccines. The individual will be responsible for ensuring all methods are performed as written and filed with regulatory agencies. The individual may conduct specific studies or projects to improve the quality or efficiency of the company’s products or procedures. The QC Analyst III will provide administrative and technical support in the absence of the QC Manager.

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Categories:Types, Resumes & CVs
Published by: Bryan Nicoll on Jul 10, 2013
Copyright:Attribution Non-commercial

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07/10/2013

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Position Title: Quality Control Analyst IIIReports To: Quality Control ManagerDepartment: Quality ControlDate Revised: April 2013FLSA Status: Non-Exempt (hourly)Summary:
 The position will include routine testing of in-process and
final container samples
for the release
of avian vaccines
.
 The individual will be responsible for ensuring all methods are performed aswritten and filed with regulatory agencies. The
individual may conduct specific studies or projectsto improve the quality or efficiency of the company’s products or procedures. The QC Analyst IIIwill provide administrative and technical support in the absence of the QC Manager.
 
Responsibilities:
1.
 
 Accurately and efficiently perform all required tests for bulk antigens, final products, and rawmaterials, as well as other procedures necessary to support company and laboratoryobjectives under cGMP and GLP guidelines to meet specified timelines.2.
 
Maintain accurate and concurrent testing records, interprets results, analyzes trends, andreports findings to the Quality Control Manager and other departments as needed. Reviewspaperwork of other analysts to ensure accuracy prior to submission to QA.3.
 
Operate and proactively maintain laboratory equipment. Ensure that equipment maintenanceis properly documented in a timely manner.4.
 
Input and report 9CFR testing results into required files and to appropriate departments.5.
 
Release antigen in the data warehouse system.6.
 
 Assist with updating, writing, and maintaining Standard Operating Procedures
bench recordsand data entry
for the department. Maintain data integrity and ensure compliance withcompany SOPs and specifications, USDA and cGMP regulations.7.
 
Continually investigate new techniques and procedures to improve the quality of testing.8.
 Communicate testing issues and priorities with the QC Manager on a daily basis.
 9.
 
Occasional weekend and off-hour work may be required.10.
 
Other duties as assigned by the Quality Control Manager.
Competencies:
1.
 
Performs all duties, procedures, techniques, and completes paperwork with persistent focuson quality and safety. Supports a culture of quality by encouraging co-workers to be diligentin the performance of each task, continually striving for accuracy. Participate at the directionof the QC Manager to support research, production, and/or other departments to achievecompany quality objectives.2.
 
Provides effective training of QC Analyst I’s and II’s, as appropriate or assigned, confirmingthat they have been properly trained on the procedure at hand and all required training
Job Description

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