Monday, January 7, 2013

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Robert Ciociola posted a job:

"Document Specialist/Coordinator 482 in Fort Washington, PA Document Specialist/Coordinator-Fort Washington, Pa 482 Contract 12-24 Months Send resumes to: bciociola@covexllc.com This position is responsible for improving and implementing key document and procedures to address consent decree work plan commitments for related to Warehouse & Distribution operations within Company PPC. This Document Specialist / Coordinator will ensure and assist work teams in creating and delivering the required documentation and procedures within a cGMP environment. This candidate will also be responsible for prioritization, coordination and collaboration of key procedure and documents between the Lancaster, Las Peidras and Fort Washington sites. • Enable and empower work teams with suggestions, solutions and a sustainable process for materials and components within company • Carry out duties in compliance with all state and federal regulations and guidelines including FDA, TUV, EPA and OSHA. • Support the ongoing consent decree work plan by: o Attending and participating in meetings related to work team activities. o Providing guidance to work teams to ensure proper solutions and gaps are addressed in conjunction with consent decree work plan due dates. o Update QSE Core Team with documentation and procedure timelines on a periodic basis. o Mitigate and remove roadblocks for Sub teams. o Escalate challenges and successes to QSE Core Team. o Promote and work within a team environment o Coordinate documentation activities with QSE 8 training coordinator for all activities related to procedures and documentation o Maintain a working knowledge of basic cGMP requirements to ensure adherence to compliance policies and regulations. • This is not an exhaustive or comprehensive listing of job functions. May perform other duties as assigned. Education: University/Bachelors Degree or Equivalent Experience/ Technical Competencies: MS Office Skills… Word, Excel and Visio Ability to drive action Technical knowledge of supply chain procedures and documentation Technical writing ability Ability to gather information, analyze and develop tactical plan Demonstrated collaboration skills Must have ability to comprehend and develop complex material specifications, component specification, materials status control, and SAP processes Must have good verbal and written skills, and proven analytical ability Job Knowledge/Skillsets: 3 + years within an operations or packaging engineering environment either within a Pharmaceutical / Medical Device or Consumer Industry. Experience within a third party or consent decree environment preferred Experience with Quality Systems, Quality Standards and Regulatory Documents Bi-lingual preferred (Spanish & English) Travel: <10% travel anticipated for this role. Contract Length: 12-24 Months http://bull.hn/l/Y22R/1"

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