Production Support Technician

Artech Information System LLC; East Hanover (NJ); On-site; USD 45,000 - 60,000; Full time

Job summary

An IT staffing company in New Jersey is looking for a candidate to manage SAP inventories and maintain compliance in a cGMP/FDA regulated environment. Responsibilities include ensuring accurate inventory status, supporting the ISO 8 Area, and performing equipment cleaning. Ideal candidates should have 1-3 years of related experience and strong communication skills. The role may require handling hazardous chemicals and being flexible with working hours, including weekends.

Qualifications

• 1-3 years of related experience in cGMP/FDA regulated industry.
• Strong interpersonal, written and communication skills required.
• Must be well organized, flexible, and work with minimal supervision.
• Ability to lift up to 50 lbs.
• Requires handling of chemicals such as corrosives, solvents & bio-hazardous materials.

Responsibilities

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

Skills

Related experience in cGMP/FDA regulated industry

Warehouse experience

Strong interpersonal skills

Problem-solving skills

Flexibility

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

• 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.

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.