Administration Officer - Kuwaiti National

What’s in it for you?!

• Tremendous career advancement opportunities!
• Excellent Medical, Dental and Vision Care including Life Insurance!
• Amazing and fun work culture, and great people to work with!
• Great work/life balance programs!
• Wellness Programs!
• 100% Matching 401k of the firs 2% and 50% of the next 4%!
• Robust PTO, holidays and community service days!
• Wide range of voluntary benefits and rewards!
• Performance base bonuses!
• Pet Insurance!

If that’s, you, apply right away! Multiple job openings hiring fast!
The Quality Control Laboratory Technician, II is responsible for daily start-up, in-process, and post-process product testing. A critical function of this role is to provide timely testing and inspection support including regular data collection (measurements), organizing data and recommended process improvements within a high-speed manufacturing production environment. The testing is vital for the production and engineering teams to ensure a target yield is achieved on the manufacturing printing presses every day. Responsible for the daily QC Lab functions, including testing of product, calibration of lab equipment, testing for raw materials and paperwork and process audits.

What you will be doing:
To perform this job successfully, a qualified individual must be able to perform each essential duty satisfactorily either with or without reasonable accommodation. The requirements listed in this job description document are representative of the knowledge, skill, and/or ability required.

• Plans and organizes priorities utilizing the Daily Priorities form.
• Responsible for timely achievement of assigned tasks and efficient time management.
• Performs and reports daily testing of product according to established methods and requirements related to raw materials test/inspection/approval/release, final release processes.
• Actively participates in the Quality Control Daily Targets related to safety, quality, delivery, and cost.
• Monitor and report test status of various production runs to Engineering Manager, Process Engineers, Area Leads, QC Manager/Supervisor and/or Manufacturing Manager.
• Identifies out-of-specification materials, including placing product on hold, proper identification, and segregation of nonconforming materials, initiating non-conforming material report (NCR) and participating in investigations.
• Provides support to Engineering, IT and R&D including participation in product/process development trials, carrying out new types of raw material and product characterization/performance testing and use of experimental materials.
• Maintains and performs necessary calibrations and re-qualification processes for lab instruments and equipment (ex: densitometers, thermocouples, thermometers, F200s, F100s, PRTs, probes, baths)
• Supports/leads calibration program activities to ensure overall Quality Management Process (QMP) compliance.
• Supports data collection activities into various forms, databases, spreadsheets and performs trend analysis of data and makes recommendations for improvements as needed.
• Verifies completeness of quality related documentation and applies risk-based thinking when evaluating processes performance results for improvement opportunities.
• Assigned technician will act as a contingency approver for quality control lab for training processes and procedures such as raw material testing and interim material (i.e., manufactured ink) approval and release.
• Follows established standard operating procedures and work instructions to evaluated manufactured products, raw materials, and intermediates.
• Support all necessary startup, in-process, and additional post process testing requirements for pilot engineering lots and manufactured production lots.
• Evaluates test data collected to support production and engineering.
• Analyzes test results and makes recommendations for production process adjustments as needed.
• Coordinate with Quality Control (QC) staff on proper testing requirements and maintain clear testing schedules for all production lots specifically managing testing schedule(s) to support timely deliveries of customer orders.
• Perform multiple tests across multiple testing equipment simultaneously (e.g., temperature baths) and maintain the accurate raw testing data files, proper testing records and appropriate documentation.
• Collaborate with operators, department leads, engineers, and supervisors on non-conforming report investigations, changes controls and corrective actions as required.
• Support QC and Engineering departments on additional testing and protocols as required for production lots, engineering studies and new product development efforts.
• Must be comfortable following procedures and performing repetitive tasks daily.
• Assists/performs internal and external audits.
• Drafts/executes change controls, CAPAs, CIs, validation test protocols and prepares required reports.
• Become an in-house subject matter expert on existing testing procedures and train for new hires.
• Maintains and adheres to all company safety policies and procedures.
• Maintains work area organization and documentation to satisfy ISO and GMP standards.
• Maintains good communication and working relationships with all departments and effectively functions within a team environment.
• Exhibits professional etiquette that exemplifies the values of the organization

Experience you will need:

• Must have High School Diploma or GED
• 1+ years related experience and/or training or a combination of equivalent education and experience.
• Experience in an ISO or GMP environment is highly desirable.
• Excellent organizational skills.
• Ability to work independently with little supervision.
• Good communication skills, written and oral.
• Ability to read and interpret data, including graphs, as they relate to test results.
• Ability to collect pertinent data, establishes facts, draw conclusions, and identify problems.
• Word processing, spreadsheet (Corel & Excel), and e-mail software in a Windows environment.