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Quality Control Inspector II - NJ
Ref No.: 18-00558
Location: Raritan, New Jersey
Start Date / End Date: 02/05/2018 to 02/05/2019
Skills
Description Level Comments
Written & Verbal Communication Skills Beginner
Sense Of Urgency Beginner
Organizational Skills Beginner
Attention To Detail Beginner
Quality Control Beginner
Quality Assurance Beginner
Microsoft Office Beginner
Lift & Carry Up To 35 Lbs. Beginner
Education
Degree Type Major/Certification Required Preferred
High School Diploma/GED active
Job Description & Requirements
Job Type: Recruited Resource - General Temp Number of Positions: 1
System Location: OCD - 6118 Created Date: 1/24/2018
Job Title: Quality Control Inspector II - NJ
CWR Type: W-2 Reason: Other
Replacement/support Gel Line
Qualifications:
A High School Diploma or a related field of study and a minimum of 3 to 5 years of experience utilizing inspection techniques. Familiarity with the guidelines and regulations of FDA, OSHA, ISO and cGMP is preferred. Be able to complete repetitive motions and stand for long periods of time are required. Diligent use of PPEs (Personal Protective Equipment) to limit exposure to bloodborne pathogens is required. Oral and written communication skills are required. Proficiency with the Microsoft Office suite of products (Excel, Word, Outlook). This position is located in Raritan, NJ. This is a second shift position and you must be able to work the following hours 7:00AM-3:30PM and have flexibility to work other shifts when necessary. Weekends and overtime are required.

Responsibilities:
Ortho Clinical Diagnostics is recruiting for a QC Inspector 2, located in Raritan, NJ. Ortho Clinical Diagnoffstics serves medical laboratories and the transfusion medicine community around the world. We're a leading provider of total solutions for screening, diagnosing, monitoring and confirming diseases early, before they put lives at risk. Our single focus is to help hospitals, laboratories and blood centers worldwide deliver results that help patients experience a better quality of life. The QC Inspector 2 will be responsible for performing production line In-Process inspections in accordance with current specifications. This person will assure compliance with company standards and applicable regulatory agencies. He/She will sample, inspect and release finished goods, perform appropriate material control in accordance with current specifications. He/She will monitor various stages of processing along with the appropriate paperwork and assure compliance with current specifications. Responsible for maintaining and storing all retains for the different products and perform quarterly destructions. He/She will be responsible for stage release of all products (tagging) to the warehouse for shipment. The QC Inspector 2 will review complaints (retains/returns) and perform AQL inspections on different products as needed. This person will assist other departments with investigations. When an event is opened and requires re-inspection, the QC Inspector 2 will train the Operators on heightened inspection. This person will be responsible for training new employees on line clearance for the different departments. He/She will provide Packaging and Labeling certification and re-certification to the Operators from different manufacturing areas. The QC Inspector 2 will make independent decisions on AQL Inspections and open non-conformances when required. The successful candidate will have the ability to prioritize and handle multiple tasks and challenges at one time and have the ability to work in a team environment and provide customer focused results in an efficient manner. The QC Inspector 2 will document results clearly and accurately. The successful candidate will adhere to departmental and ORTHO SOP's and safety requirements as well as be accountable for notifying management of any out of specifications or abnormalities in a timely manner. He/She will be accountable for reporting nonconformance's to management immediately. The QC Inspector 2 will provide support during regulatory inspections. Edit documentation (i.e. Standard Operating Procedures, batch records, etc.). Understands and applies PE tools in daily work activities. The QC Inspector 2 will be familiar with ORTHO safety and environmental policies and perform work tasks and operations in compliance with all safety and environmental rules and regulations, and encourage co-workers to do so; if uncertain, consults with supervisor. Attend applicable safety and environmental education and training programs and attend departmental safety and environmental meetings. Immediately report and correct, if possible, unsafe conditions, spills and near miss incidents. Conduct self-inspections of workstations and offices for hazardous conditions.

Attached Documentation:



QC Inspector 2
Job Description:
Ortho Clinical Diagnostics is recruiting for a QC Inspector 2, located in Raritan, NJ.

Ortho Clinical Diagnoffstics serves medical laboratories and the transfusion medicine community around the world. We're a leading provider of total solutions for screening, diagnosing, monitoring and confirming diseases early, before they put lives at risk. Our single focus is to help hospitals, laboratories and blood centers worldwide deliver results that help patients experience a better quality of life.

The QC Inspector 2 will be responsible for performing production line In-Process inspections in accordance with current specifications. This person will assure compliance with company standards and applicable regulatory agencies. He/She will sample, inspect and release finished goods, perform appropriate material control in accordance with current specifications. He/She will monitor various stages of processing along with the appropriate paperwork and assure compliance with current specifications. Responsible for maintaining and storing all retains for the different products and perform quarterly destructions. He/She will be responsible for stage release of all products (tagging) to the warehouse for shipment. The QC Inspector 2 will review complaints (retains/returns) and perform AQL inspections on different products as needed. This person will assist other departments with investigations. When an event is opened and requires re-inspection, the QC Inspector 2 will train the Operators on heightened inspection. This person will be responsible for training new employees on line clearance for the different departments. He/She will provide Packaging and Labeling certification and re-certification to the Operators from different manufacturing areas. The QC Inspector 2 will make independent decisions on AQL Inspections and open non-conformances when required. The successful candidate will have the ability to prioritize and handle multiple tasks and challenges at one time and have the ability to work in a team environment and provide customer focused results in an efficient manner.
The QC Inspector 2 will document results clearly and accurately. The successful candidate will adhere to departmental and ORTHO SOP's and safety requirements as well as be accountable for notifying management of any out of specifications or abnormalities in a timely manner. He/She will be accountable for reporting nonconformance's to management immediately.
The QC Inspector 2 will provide support during regulatory inspections. Edit documentation (i.e. Standard Operating Procedures, batch records, etc.). Understands and applies PE tools in daily work activities.
The QC Inspector 2 will be familiar with ORTHO safety and environmental policies and perform work tasks and operations in compliance with all safety and environmental rules and regulations, and encourage co-workers to do so; if uncertain, consults with supervisor. Attend applicable safety and environmental education and training programs and attend departmental safety and environmental meetings. Immediately report and correct, if possible, unsafe conditions, spills and near miss incidents. Conduct self-inspections of workstations and offices for hazardous conditions.
All ORTHO employees are required to cultivate an environment of quality & compliance in their actions. This includes attending all required training, adhering to the processes & procedures of their role and the company and displaying the highest level of integrity.
Qualifications:

A High School Diploma or a related field of study and a minimum of 3 to 5 years of experience utilizing inspection techniques. Familiarity with the guidelines and regulations of FDA, OSHA, ISO and cGMP is preferred. Be able to complete repetitive motions and stand for long periods of time are required. Diligent use of PPEs (Personal Protective Equipment) to limit exposure to bloodborne pathogens is required. Oral and written communication skills are required. Proficiency with the Microsoft Office suite of products (Excel, Word, Outlook). This position is located in Raritan, NJ. This is a second shift position and you must be able to work the following hours 7:00AM-3:30PM and have flexibility to work other shifts when necessary. Weekends and overtime are required.



Work Location: 1001 US Highway 202 USRAR, Raritan, NJ 08869 United States
Start Date: 2/5/2018 Work Days:
Sun Mon Tue Wed Thu Fri Sat
End Date: 2/5/2019
Start Time: 7:00 AM Total Reg Hours: 40.00
End Time: 3:30 PM Overtime Required:
Lunch Time: 30 Minutes
Exempt: