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Quality Assurance Coordinator

Posted: January 27, 2025
Salary:Up to US$25 per hour
Location:Alsip
Job type: Contract
Discipline:Medical Device
Reference:238748_1738013708
Work Location:On-site

Job description

Are you ready to give your career a boost by bringing your talents and expertise to some of the nation's top companies? Let Medix partner with you to give you the edge you need! We currently have excellent assignments within Life Science, Engineering, and Healthcare, all in fast-paced environments. See details below and apply now if interested as we are hiring immediately!

QA Coordinator

Details

QA Coordinator

Alsip, IL 60803

Pay: $25/HR

Shift: M-F, 8AM to 4:30PM

**Contract to hire!***

QUALIFICATIONS:

  • Bachelor of Science in related field is preferred
  • 2-3 Years experience in document control, quality assurance, ect
  • Medical Device industry experience preferred
  • Strong computer skills (Microsoft Office suite)

RESPONSIBILITIES:

  • Review production records, including batch records, bar code labels, and inspection sheets.
  • Visually inspect samples of finished goods to ensure compliance with established procedures and quality standards.
  • Investigate and resolve discrepancies, ensuring adherence to quality requirements.
  • Track non-standard batch numbers (e.g., multiple batch pairings or kit component updates) to ensure conformance with pairing and component procedures.
  • Support the document control process across all stages of its cycle.
  • Execute daily management of QMS processes by investigating trouble reports and implementing necessary improvements.
  • Assign and verify trouble reports to responsible team members, ensuring timely resolution.
  • Assist with process trouble reports and Corrective and Preventive Action (CAPA) investigations.
  • Support activities related to nonconformities and complaints, as needed.
  • Prepare and submit standard reports, Key Performance Indicator (KPI) data, and related evidence to peers or superiors as per schedule.
  • Compile and provide data for QMS Management Reviews.
  • Participate in external audits (e.g., ISO, FDA) as a subject matter expert for QMS processes.
  • Manage responses to audit non-conformities related to QMS processes.
  • Provide QMS training to operations and other departments as needed.
  • Participate in Global Quality Management (GQM) improvement activities, including high-priority Key Initiative (KI) projects.
  • Successfully perform all essential duties and responsibilities listed above.
  • Reasonable accommodations will be provided to enable individuals with disabilities to fulfill the essential functions of this role.

Benefits

Supplemental medical, Dental, Vision coverage

Term life Insurance plan

PTO accrual

401K

QC Coordinator

Apply Now!

#MedixScience

For California Applicants:

We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance (FCIHO), Los Angeles Fair Chance Ordinance for Employers (ULAC), The San Francisco Fair Chance Ordinance (FCO) , and the California Fair Chance Act (CFCA).

This position is subject to a background check based on its job duties, which may include patient care, working with vulnerable populations, access to financial and confidential information, driving, working with heavy machinery, or working in a warehouse or laboratory environment. Due to these job duties, this position has a significant impact on the business operations and reputation, as well as the safety and well-being of individuals who may be cared for as part of the job position or who may interact with staff or clients.