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Quality Systems Associate

Job in Colorado Springs, El Paso County, Colorado, 80509, USA
Listing for: Grifols, S.A
Full Time position
Listed on 2026-01-22
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
  • Healthcare
    Data Scientist
Job Description & How to Apply Below

Quality Systems Associate

Pay scale of $/hour
, depending on training, education and experience. This position is eligible to participate in up to 5% of the company bonus pool. We offer benefits including medical, PTO, up to 5% 401K match, and tuition reimbursement. We are committed to offering our employees opportunities for professional growth and career progression. Even though we are a global healthcare company with employees in 30 countries, Grifols prides itself on its family‑like culture.

Our company has more than tripled its workforce in the last 10 years —we're growing, and you can grow with us!
Final date to receive applications DATE = 01/26/26 @ 11:59PM LOCAL TIME .

Summary

Under the direct supervision of the Quality Systems Manager, perform quality assurance and Training functions to ensure compliance with internal and external regulations and protocol.

Primary Responsibilities
  • Completes weekly review of equipment QC and maintenance records.
  • Documents, investigates, and performs root‑cause analysis for deviations and customer complaints, specifically in how they relate to product quality and/or donor safety.
  • Inspects and releases incoming supplies. Investigates and reports supplies that have not met quality specifications and requirements prior to use.
  • Performs documentation review for unsuitable test results.
  • Assists the Quality Systems Manager to ensure that cGMP regulation, SOPs and regulatory requirements are followed.
  • Performs all product release activities.
  • Reviews lookback information and documentation.
  • Reviews waste shipment documentation.
  • Reviews unexpected plasmapheresis events including electronic donor chart and related documentation pertaining to exceptions occurring during the donation process.
  • Reviews electronic donor chart exceptions impacting donor eligibility/safety and/or product quality.
  • Reviews donor deferral notifications from competitor centers.
  • Reviews plasma processing documentation to ensure the proper freezing, storage and handling of product.
  • Creates, maintains, and audits training records and files to ensure compliance.
  • Performs employee training observations to ensure staff competency prior to releasing employees to work independently.
  • Conducts required training activities for Center Notifications, Corporate Directives, SOP changes, and initial SOP implementations.
  • On an occasional basis, when the Quality Systems Manager is absent, may need to perform the following duties:
    • Reviews and approves deferred donor reinstatement activities.
    • Assists with completion of the internal donor center audit.
Additional Responsibilities
  • Performs review of monthly trending report.
  • Performs review of donor adverse events reports and the applicable related documentation.
  • Conducts training to address donor center corrective and preventative measures.
Knowledge, Skills, and Abilities

Developing command of interpersonal communication, organizational and problem‑solving skills. Ability to understand FDA regulations. Strong integrity and commitment to quality and compliance. Good knowledge of mathematics. Legible handwriting. Proficiency with computers. Ability to work flexible scheduling to meet business needs. Performs basic document review and employee observations. Communicates openly with the CQM on issues noted during reviews. Ability to understand and follow SOP’s and protocols.

Ability to perform primary responsibilities of the Quality Associate role in a proficient manner. Has a basic understanding of cGMP and quality systems. Is able to spend hours sitting and reviewing documentation for accuracy. Demonstrates good organizational skills and attention to detail.

Education

High school diploma or GED. Obtains state licensures or certifications if applicable.

Experience

Typically requires no previous related experience.

Occupational Demands

Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 °F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold‑gear. Work is…

Position Requirements
10+ Years work experience
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