Senior QC Sterility Associate | Lab Instrumentation

Grifols

North Carolina

On-site

USD 65,000 - 90,000

Full time

14 days+
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Job summary

Grifols is seeking a Quality Associate II-III/Sr. Quality Associate I, QC (Sterility) to support routine QC Sterility testing, data analysis, and shift coordination. The role includes training, SOP adherence, and cross-functional collaboration within the Sterility laboratory environment.

The ideal candidate has a STEM degree with lab experience, SAP proficiency, and strong organizational skills to manage complex testing workflows and maintain compliance with cGMP standards.

Qualifications

  • BA/BS in STEM with 2+ years of relevant experience.
  • Experience testing/gowning/operating in a classified environment.
  • Proficiency using SAP strongly preferred.
  • Detail oriented with strong organizational and communication skills.
  • Ability to prioritize, multitask and lead; related experience considered.

Responsibilities

  • Collects, reviews, and analyzes data.
  • Coordinates work activities and scheduling.
  • Coordinates employee training.
  • Communicates effectively across the organization.
  • Oversee instrumentation within the QC Sterility lab.
  • Troubleshoot issues and support testing analysts.
  • Manage qualification/installation of new instruments.
  • Prepare analytical reports and method validations.
  • Collaborate cross-functionally on projects.

Skills

Detail oriented
Leadership
Communication
Gowning procedures

Education

BA/BS in STEM
Equivalent education/experience

Tools

SAP
Microsoft Excel
Microsoft Word

Job description

Grifols is seeking a Quality Associate II-III/Sr. Quality Associate I, QC (Sterility) to support routine QC Sterility testing, data analysis, and shift coordination. The role includes training, SOP adherence, and cross-functional collaboration within the Sterility laboratory environment.

The ideal candidate has a STEM degree with lab experience, SAP proficiency, and strong organizational skills to manage complex testing workflows and maintain compliance with cGMP standards.

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