Sr. Manufacturing Supervisor - SORC - (US-PA-West Point - 19486)

Minimum Education: Tech School
Job Type: Full Time
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Merck & Co. Inc. established in 1891 is a global research-driven pharmaceutical company dedicated to putting patients first.

Join us and experience our culture first-hand - one of strong ethics & integrity diversified experiences and a resounding passion for improving human health. As part of our global team youll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.

This high impact role in Merck Manufacturing assures that products manufactured comply with cGMPs operating procedures and other applicable regulations. The incumbent will supervise the direct processing of materials and the associated hourly workforce to insure compliance and realize business results. The incumbent will effectively collaborate with and manage a work team with specific responsibility for motivating others ensuring performance schedule execution task coordination equipment and area preparation and effective administration of personnel policies and procedures. Ability to manage conflict and support resolution to technical and personnel challenges is key as is openness to change and ability to effect positive change.

Because our business is dynamic and advances in science and technology require new methods of production we are looking for individuals who can do the following: Collaborate with team members in the identification and implementation of continuous improvement initiatives and action plans. Support activities in the areas of compliance cost containment efficiency productivity energy conservation waste minimization operational excellence and lean practices.

Due to the high impact nature of this role it is essential that the incumbent demonstrate integrity credibility and flexibility in their daily performance so as to motivate others to do the same.

Manufacturing Supervisor

In this role you will assure compliance with safety and environmental practices cGMPs and SOPs in the work area. Participate in external and internal audits and inspections. Initiate the investigation when a quality or safety event occurs during the shift. Work with members from Quality and Technical Operations to properly handle unplanned events. Ensure that corrective actions are implemented.

Experience/Skills:

Minimum 2 years working experience in cGMP or equivalent environment
Willingness to work off-shift or weekends
Computer literacy in MS Office Word Outlook Excel

Assets (Preferred):

Manufacturing Supervisor (M08)
Education:

B.S. with emphasis in Science or Engineering

ExperiencecGMP experience in a sterile bulk or finished pharmaceutical environment.
Supervisory experience in a heavily regulated industry (ex. FDA Military Nuclear Petro-Chemical)
Manufacturing plant experience in operational capacity
Experience working within a Union environment
Experience with working in SAP or other Enterprise software
Technical writing experience related to manufacturing investigations

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