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Show me jobs like this one| Job Ref: | 6176 |
| State: | Maryland (MD) |
| City: | Frederick |
| Post Code: | Dec 08, 2011 |
| Job Description: |
The Upstream Manufacturing group of MedImmune in Frederick, MD, is seeking an experienced Production Supervisor to join their team. This will be a night-shift position. This person will be supervising individuals from their immediate team. Scope (Tasks/Activities): * Responsible for overseeing the accurate and timely completion of clinical and commercial manufaturing campaigns and the associated cGMP documentation * In conjunction with management personnel, participates in the technical transfer, planning, implementation and maintenance of manufacturing processes and procedures * Serves as the lead investigator or primary point of contact for non-conformances * Reviews Manufacturing Production Records (MPRs), Standard Operating Procedures (SOPs), and Solution Production Records (SPRs) * Prepairs daily operational schedule * Ensures the effective use of material, equipment and personnel in the manufacture of clinical and commercial product * Approves MPRs, SOPs, and SPRs, as requested * Ensures training records for subordinates are accurate and current * Ocersees the performance management process for subordinates * Supports organizational excellence initiatives * Initiates and leads presentations/discussion of technical information concerning specific projects, schedules, ets. * Oversee the implementation and compliance with MedImmune's safety standards Knowledge Requirements: * Demonstrates knowledge of MedI's human resources policies, practices, and systems such as: o Recruit Point, o Insight, o SuccessFactors. * Demonstrates general knowledge of organizational excellence principals Problem Solving: * Regularly works on non-routine assignments in functional area where the ability to assess/analyze identifiable factors, situations and/or data is required Freedom To Act: * Works under minimal supervision from area management * Resolves daily operational issues within own functional area and escalates more complex issues to area management * Adheres to Good Manufacturing Practices and standard operating procedures * Interacts regularly with subordinates, other production sub-groups, functional area peers, and area management Impact: * Erroneous decisions could negatively impact personnel, schedule, budget and/or materials * Effects of decisions are long-lasting and influence the future course of the organization. Required Education/Experience: Bachelor's degree in the sciences or engineering is strongly preferred. The appropriate candidate should have 7+ years' experience in a large-scale biotechnology manufacturing environment. Requirements
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| Post Date: | 12/09/2011 |
