Artech Information System LLC
Production Support Technician
Artech Information System LLC, East Hanover, New Jersey, us, 07936
Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.
Job Description
Ensure accurate SAP inventories are maintained for all components. Proper status segregation and storage of media lots. Support the maintenance of an “audit ready” state of the ISO 8 Area. Timely response to all module requests. Batch Records are properly kitted and staged based on production schedule. All gowning materials in the ISO 8 area are maintained to adequate levels. ISO 8 area has ample supply of non-inventory items. Logbook entries are clear and complete. Kanban system is utilized to ensure FIFO. Equipment cleaning is performed as required. Ensure Batch records are reviewed and corrected in a timely manner. Qualifications
Skills: 1-3 years of related experience in cGMP/FDA regulated industry. Warehouse experience preferred. Qualifications: Strong interpersonal, written and communication skills along with problem solving and follow-up skills are required. Must be well organized, flexible and work with minimal supervision. Ability to lift up to 50 lbs. Alternate shifts, weekends and overtime will be required. Requires handling of chemicals such as corrosives, solvents & bio-hazardous materials.
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Ensure accurate SAP inventories are maintained for all components. Proper status segregation and storage of media lots. Support the maintenance of an “audit ready” state of the ISO 8 Area. Timely response to all module requests. Batch Records are properly kitted and staged based on production schedule. All gowning materials in the ISO 8 area are maintained to adequate levels. ISO 8 area has ample supply of non-inventory items. Logbook entries are clear and complete. Kanban system is utilized to ensure FIFO. Equipment cleaning is performed as required. Ensure Batch records are reviewed and corrected in a timely manner. Qualifications
Skills: 1-3 years of related experience in cGMP/FDA regulated industry. Warehouse experience preferred. Qualifications: Strong interpersonal, written and communication skills along with problem solving and follow-up skills are required. Must be well organized, flexible and work with minimal supervision. Ability to lift up to 50 lbs. Alternate shifts, weekends and overtime will be required. Requires handling of chemicals such as corrosives, solvents & bio-hazardous materials.
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