We are not offering you a job, but rather we are offering you a workplace that feels like home at Greiner Bio-One.

In-Process Quality Inspector II

Location: 

Monroe, US, 28110

Travel activity:  N/a
Employment Type:  Permanent

Your challenge

Responsibility:
The IPQ Inspector II is responsible for the daily monitoring and inspection of product during manufacturing. The IPQ Inspector II works under the guidance of senior IPQ Inspectors, IPQ Team Lead, and Supervisor and is responsible for ensuring compliance with Quality Management Systems policies and procedures, regulatory standards, and  inspection of GBO NA products. The role will be assigned to a 2-2-3 Twelve Hour Shift Schedule.
 
Responsibilities include:
•    Coordinating and performing IPQ inspection and release for injection molding pre-analytic components and pre-analytic assembly/finished product according to valid procedure(s).
•    Performing timely measurement and reporting for in-process inspections.
•    Inspections methods include sampling per statistical/interval plans, visual characterization, dimensional measurements, and functional evaluations using analytical equipment.
•    Provide on-the-job training for IPQ team members according to qualified skills and valid procedures with escalation to senior personnel for final qualification approvals.
•    Demonstrated proficiency and qualification to independently identify and handle non-conformance notifications according to valid procedure(s). 
•    Progressive training and qualification performing suitability checks and measurement device verifications.
•    Progressive training and qualification performing IPQ inspection and release for injection molding bioscience and barcode product.
•    Accurately documenting and submitting IPQ inspection records following Good Manufacturing Practice (GMP). 
•    Support maintenance and organization of testing stations, equipment, and work areas to support operational readiness and hygiene  requirements.
•    Perform periodic cycle counting and request submission to order IPQ supplies as needed. 
•    Performing other administrative duties to ensure IPQ operational readiness as required.
Authority includes:
•    Conduct in compliance with GBO NA Safety, Quality, HR, and payroll policies with management escalation to the IPQ Team Lead and Supervisor.
•    The evaluation and reporting of product inspected, control of non-conforming products, and IPQ release according to valid procedures.

Your Profile

Job Requirements:
The following criteria are considered minimums for the role:
•    High School diploma or GED; Associate’s Degree in Science, life sciences, or related field preferred
•    Experience in an ISO 9001, ISO 13485, or similar regulated manufacturing environment preferred
•    Minimum 1-3 year direct Quality Control experience
•    Entry level experience with laboratory testing equipment, instrumentation, and analysis, as well as laboratory data processing and review
•    Basic-level MS office skills 
•    Basic-level knowledge of statistics, calculations, and reporting

We provide equal opportunities for everyone and see diversity as our strength. Therefore, we welcome all applicants – regardless of identifying characteristics such as gender, age, background, social status, veteran status, sexual orientation, religion, or mental and physical abilities. We have additionally set the goal of empowering women and increasing female leader representation. We foster an inclusive work environment and encourage all individuals to apply.

Job ID:  3341

About Greiner Bio-One

Greiner Bio-One feels like home.

For visionaries with drive and ideas, for team players who share their knowledge and entertain new ways of thinking, for people who (are able to laugh at themselves and) strive for excellence. Our door is always open to achievers, doers and hidden talents who want to make a difference.

We have future in our blood.


Nearest Major Market: Charlotte