Contract: West Point, Pennsylvania, US
Salary: $41.00 Per Hour
Job Code: 346937
End Date: 2024-04-14
Job Status: Expired
Qualifications:•B.S./M.S. degree in appropriate engineering/scientific field•Minimum of 0-3+ years post-Bachelors degree experience in a cGMP environment (e.g. Production, Development, Process Engineering, Technical Services or related field) in pharmaceutical/ biotech industry•Previous experience in writing investigations for atypical events in a manufacturing environment•Experience in Bulk/Drug substance Manufacturing). In addition to Deviation Management, will be authoring updates to Batch Records and Standard Operating Procedures.Responsibilities:•Primary responsibilities include day-to-day technical support to manufacturing operations, including resolution and reduction of process deviations, development and implementation of corrective/preventative actions, and leading manufacturing investigations•This Individual will also develop working relationships with counterparts in other areas supporting aseptic manufacturing, testing, planning, and release and is required to utilize sound scientific and engineering principles to investigate process deviations•Troubleshooting and root cause analysis of laboratory test failures and manufacturing atypical events, development of corrective/preventative actions is required•Analysis of complex problems through critical analytical thinking
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