Our client, one of the largest pharmaceutical companies in the U.S., is looking for a Deviation Management Specialist - I which is located at West Point, PA. The client is seeking candidates with deviation investigation experience and technical writing experience.

　　Job Title: Deviation Management Specialist - I

　　Location: West point, PA

　　About the Role:

　　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 End-to-End (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 site-based assignment and requires the employee to work at the site M-F.

　　Requirements:

　　Education Minimum Requirements: • B.S. degree in Engineering or Sciences.

　　Minimum one (1) year post-bachelor’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.

　　Vaccine manufacturing

　　Sterile processing

　　Experience authoring

　　If this is a role that interests you and you’d like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!

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