Production Support Technician

Artech Information System LLC; Morris Plains (NJ); On-site; USD 50,000 - 70,000; Full time

Job summary

A mid-sized IT staffing firm in Morris Plains, New Jersey, is seeking a candidate for a role focused on ensuring adequate supply and kitting in the ISO 8 area. Responsibilities include maintaining SAP inventory, supporting audit readiness, and preparing Batch records according to production schedules. Candidates should have 1-3 years of experience in a cGMP/FDA regulated industry and possess strong communication skills. This position requires lifting up to 50 lbs and may involve alternate shifts and handling chemicals.

Qualifications

• 1-3 years of related experience in a cGMP/FDA regulated industry.
• Strong interpersonal, written and communication skills.
• Ability to lift up to 50 lbs.

Responsibilities

• Ensure accurate SAP inventories are maintained for all components.
• Support the maintenance of an audit-ready state of the ISO 8 Area.
• Ensure Batch records are reviewed and corrected in a timely manner.

Skills

cGMP/FDA regulated industry experience

Warehouse experience

SAP knowledge

Job description

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

This role ensures that all components are adequately supplied and kitted to adhere to the production schedule along with handling media related activities within the ISO 8 area.

Major Accountabilities

ISO 8 Activities:

• 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.
• Logbooks 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.

Skills:

• 1-3 years of related experience in cGMP/FDA regulated industry.
• Warehouse experience preferred.
• SAP knowledge preferred.

Other 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.