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Senior Manufacturing Quality Inspector

ICU Medical


Job Location:

Austin, TX - USA

Monthly Salary: Not provided by the employer
Posted: 29 September 2026 (5 days ago)
Application Deadline: 27 December 2026
Vacancies: 1 Vacancy

Job Summary

Description

Position Summary

The Final Quality Assurance performs audit review on each batch record to ensure completeness and compliance before final release of audit to assure the product has been manufactured in accordance with established quality Quality Assurance is responsible to retain all batch records per retention procedure.

3rd shift: Sunday - Wednesday (6:00pm - 4:30am)

Essential Duties & Responsibilities

  • Perform audits on each batch record to ensure completion and compliance (in hard copy or electronic version)
  • Execute final product release via iFactory / Oracle system
  • Access to Oracle Installed Base to update serial device information
  • Provides Manufacturing / MQA support to detect quality risks
  • Verify that the records documented are within the corresponding procedures
  • Demonstrate leadership problem solving skills and technical knowledge with solid communication skills attitude dedication and commitment
  • Ensures departmental compliance to all Federal State Local and Company regulatory requirements. These elements include FQA EPA FDA OSHA ISO EEPC and Company policies relative to the manufacture of product lot control requirements documentation requirements housekeeping preventative maintenance calibration associate training and safety (equipment associate)
  • File and retain batch records in controlled area per retention procedure
  • Ability to troubleshoot and work in a team environment
  • Other activities related to the position

Knowledge Skills & Qualifications

  • Excellent Mathematical knowledge
  • Good knowledge in records filing
  • Good computer knowledge
  • Ability to comprehend both verbal and written instructions

Education and Experience

  • High School Diploma or GED required
  • Experience with medical devices/pharmaceutical GMPs preferred
  • Minimum of 2 years in a FDA regulated manufacturing environment

Minimum Qualifications

  • Must be at least 18 years of age

Travel Requirements

  • Typically requires travel less than 5% of the time

Physical Requirements and Work Environment

  • While performing the duties of this job the employee is regularly required to talk hear and communicate on phone and through email.
  • While performing the duties of this job the employee is regularly required to sit which is mainly on the computer with some standing during shift
  • Must be able to repetitively move and lift objects of up to 20 lbs



Required Experience:

Senior IC


About Company

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Innovation, Impact, and Purpose. Find Your Future Here. We manufacture the critical IV solutions providers count on to deliver consistent, reliable care. Each product we make helps ensure patients receive the therapies they need without disruption. When you work here, you become part ... View more

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