drjobs Deviation Management Specialist - I Assistant

Deviation Management Specialist - I Assistant

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1 Vacancy
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Job Location drjobs

West Point - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Qualifications Education Minimum Requirements: B.S. degree in Engineering or Sciences. Required Experience and Skills: Minimum one (1) year postbachelor s degree experience in a GMP (good manufacturing practices) manufacturing and/or technical support of GMP manufacturing operations (or M.S. degree with < 1 year experience). Demonstrated ability to drive results to hit assigned due dates. Strong communication collaboration skills and ability to drive accountability. Strong problemsolving skillset Preferred Experience and Skills: Vaccine manufacturing Sterile processing Experience authoring
Responsibilities The Deviation Management Contractor will be responsible for deviation management activities in support of vaccine production at the West Point site. This engineer will be a member of the Technical Operations Deviation Management team within the ROTA EndtoEnd (E2E) technical operations unit. The primary responsibility of the individual will be investigation initiation and closure associated with vaccine technology/production in support of the operations taking place in the ROTA E2E. Support will be focused on the Deviation Management process including operations support equipment troubleshooting implementation of process/equipment actions and other related duties. This position will require development of technical expertise of process and product knowledge. This is position is a sitebased assignment and requires the employee to work at the site MF. Two days of remote work per week may be available work permitting but is not guaranteed. Offshift or weekend coverage may be required based on business unit needs and specific assignments. Responsibilities include: Leads and/or works as a team member on manufacturing investigations and/or process improvement projects. Has ability to examine an issue from diverse perspectives (safety compliance automation equipment process and people) in order to identify root cause and propose effective corrective and preventative actions (CAPAs). Assures consistent application of standardized work engineering and process tools. Provides technical support to manufacturing shop floor for problems and issues. Conducts and designs experimental protocols as needed using the Technical Operations lab facilities and/or production equipment at full scale. Writes technical documents to support closure of deviations using the SAP system. Authors and updates technical and manufacturing documents necessary for investigations process design/definition engineering studies process demonstrations change control and validation.
System Location: Manufacturing (Z007) Required
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CWR Type: W2 Required

Employment Type

Full Time

Company Industry

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