Inspector, Final QA

Aquí es donde salvas y sostienes vidas

En Baxter, estamos profundamente conectados por nuestra misión. No importa tu rol en Baxter, tu trabajo tiene un impacto positivo en la gente alrededor del mundo. Sentirá un propósito en toda la organización, ya que sabemos que nuestro trabajo mejora los resultados para millones de pacientes.

Los productos y terapias de Baxter se encuentran en casi cada hospital del mundo, el clínicas y en los hogares. Por más de 85 años hemos sido pioneros en innovaciones médicas significativas que transforman el cuidado en salud.

Juntos creamos un lugar donde somos felices, exitosos y nos inspiramos mutuamente. Aquí es donde puedes hacer tu mejor trabajo.

Únete a nosotros en la intersección de salvar y sostener vidas-donde tu propósito acelera nuestra misión.

Your role at Baxter
This document outlines the employment prerequisites and job responsibilities for the Inspector, Final QA position

What you'll be doing
 Perform the inspection of Device History Record (DHR) documentation for infusion pumps and wireless battery modules either on paper or in the electronic Manufacturing Execution System Camstar to ensure test procedures have been completed and release specifications are within specifications for final acceptance and release.
 Perform inspection of the pump or wireless battery module to ensure all visual aspects, including approved labels, are met prior to release of the pump or wireless battery module.
 Approves the release of the pump and wireless battery modules in the appropriate ERP system, as applicable (JDE B4ONE, JDE GME)
 Ensures there are no open nonconformances associated with the pump or wireless battery modules in the approved nonconformance tracking system.
 Reviews the device history log within a pump to ensure final testing has been completed in accordance to the applicable procedure.
 Accurately record all failing observations using the rework form in Camstar or the nonconformance system as applicable.
 Dispositions the rework activities of nonconformances and completes the electronic approval and closure process for any non-conformances with the device in the approved electronic system.
 Ensure process control and maintenance procedures are being followed.
 Recognize out of compliance/out of tolerance situations and take appropriate action.
 Inspect Service Parts and approve release of the parts.
 Assist with identification and containment of nonconforming product on the floor for internal investigations and holds.
 Perform other duties as assigned.

What you'll bring

 High School diploma or GED.
 Preferred experience in a pharmaceutical or Biotech industry helpful.
 Must be familiar with cGMP and FDA requirements.
 Knowledge and working application of the following:
 Measurement equipment.
 cGMP documentation and FDA
 Basic ESD requirements
 Computer based programs
 Data entry and spreadsheet applications.
 Perform repetitive motions with hands/fingers.
 Demonstrated attention to details and accuracy, required.
 Must have good communication skills.
 May be required to work flexible hours and overtime on short notice.
 Ability to visually inspect and identify particulate/foreign matter and distinguish between colors as required by FDA Current Good Manufacturing Practices.

We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all our employees, and we strive to be more transparent with our pay practices. To that end, this position has a salary pay rate of $26.75. The pay rate is based on several factors including, but not limited to, relevant skills/experience, time in the role, business line, and geographic/office location

PHYSICAL DEMANDS
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee:
 Must be able to sit for most of the workday.
 Ability to stand or walk for long periods as well.
 Must have good hand to eye coordination and dexterity.
 Physical Requirements: Dynamic Lifting capability: Must have the ability to lift and carry 25 pounds. Must also have the capability to push and pull a maximum force of 5 pounds 4 feet.

VI. WORK ENVIRONMENT
Work environment characteristics described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made