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Baxter Sr Inspector, QA - Label Control in Bloomington, Indiana

Sr Inspector, QA - Label Control

Req #:

JR - 031840

Location

Bloomington, Indiana, United States

Job Category:

Quality Control

Date Posted:

02/02/2021

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Overview

This is where you make a difference in our patients’ safety. As a member of the Baxter Quality team, you will play an essential part in our mission of saving and sustaining lives. Quality is important throughout the entire product lifecycle and works collaboratively with all areas of the organization. Because Quality touches everything Baxter does, a role in Quality provides many opportunities for growth, learning and a successful career that has a daily impact on people’s lives.

  • Support for Parents

  • Continuing Education/Professional Development

  • Employee Health &Well-Being Benefits

  • Paid Time Off

  • 2 Days a Year to Volunteer

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Success Profile

What makes a successful Quality team member at Baxter? Take a look at some of the top traits we’re looking for and see if you’re a fit.

  • Detail Oriented

  • Continuous Learner

  • Courageous

  • Collaborative

  • Critical Thinker

  • Influential

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Sr Inspector, QA - Label Control

This is where you save and sustain lives

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You’ll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxter’s products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining lives— where your purpose accelerates our mission.

Summary:

The Sr. Quality Inspector (Label Control) is a member of the Finishing Quality Assurance Team reporting directly to the Quality Finishing Line Operations Supervisor. The Sr. QA Inspector (Label Control) is responsible for printing, counting, inspecting, and issuing all client specific printed materials for pharmaceutical products. He or she is expected to meet client demand with first pass quality using controlled documentation (batch records, Finishing Specification Sheets, Master labels, standard operating procedures) and current Good Manufacturing Practices (cGMP) guidelines. In addition, the Sr. Quality Inspector will ensure the accuracy of inventory counts and provide training for new Label Control employees. The Sr. QA Inspector (Label Control) is expected to contribute to an environment where teamwork, productivity, safety, identity, strength, purity and quality (SISPQ) are reflected in the finished product.

Essential Duties and Responsibilities (these are primary responsibilities of the role and the incumbent will perform other duties as assigned):

  • Calculate quantity of each Printed Material required for each batch

  • Set up print jobs and ensure accuracy of all in-house Printed Material

  • Assemble all required Printed Materials and imprint devices for each batch as directed by the Finishing Specification Sheet

  • Document, issue, and release all Printed Materials

  • Return Printed Materials to inventory as appropriate

  • Perform resupplies of materials

  • Clearance of print stations

  • Ensure organization and maintenance of the Label Control Cage

  • Participate in process improvement teams for Label Control activities

  • Act as the first point of contact for any printed materials/Label Control issues that occur

  • Perform inventory cycle counts in the enterprise resource planning system.

  • Cross train on the basic job skills for both QA Finishing Line Operations and the QA Warehouse Technician (including line clearance, AQL inspection, and Reserve Sample Inspection)

  • Perform QA Checklist Assessments to ensure compliance of all areas in the Finishing department. Job Requirements (Education, Experience and Qualifications):

  • High School diploma or GED required

  • Minimum 2 years experience in a pharmaceutical or biotech industry required.

  • General Knowledge of quarantine and warehouse operation Preferred.

  • Must be able to become forklift certified

  • Computer proficiency in Microsoft Word, Excel, and Outlook and the ability to use enterprise software (examples include: JDE, BPLM, Pilgrim, Trackwise, etc.) Physical / Safety Requirements

  • Must be able to lift 30 lbs.

  • Must be able to qualify to 20/25 corrected vision and pass color blindness testing.

  • Must be able to perform pallet wrapping and clearance tasks, including bending, twisting, kneeling and stooping.

  • Must be able to sit and stand for extended periods of time.

  • Must wear appropriate personal protective equipment as applicable.

  • Duties may require overtime work, including nights and weekends.

  • Use of hands and fingers to manipulate office equipment is required.

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Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

EEO is the Law

EEO is the law - Poster Supplement

Pay Transparency Policy

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please send an e-mail to

[email protected]

and let us know the nature of your request along with your contact information.

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