We use cookies. Find out more about it here. By continuing to browse this site you are agreeing to our use of cookies.
#alert
Back to search results
New

Associate Quality Assurance

Spectraforce Technologies
United States, North Carolina, Holly Springs
Jul 15, 2026
Job Title: Associate Quality Assurance

Duration: 6 Months( PE)

Location: Holly Springs, NC

Note:

  • Fully Onsite
  • Dayshift, 8:00 AM or earlier start time


Ideal Candidate:

  • Local Candidates - Not open to relocation candidates
  • 4-5 years of industry experience
  • QA and GMP experience
  • Raman Technology experience
  • Onsite 5 days a week.


Job Details

We are seeking a Quality Assurance Senior Associate to support the client North Carolina (ANC) Quality Assurance team. This role provides dual-function support across Incoming Quality Assurance (IQA) and Warehouse QA floor operations, ensuring raw materials and warehouse activities comply with cGMP, internal procedures, and quality standards.

The position includes real-time QA oversight on the warehouse floor, execution of inspection, sampling, and Raman spectroscopy testing for IQA, and serving as a primary QA contact for event triage and deviation management.

Basic Qualifications

  • High School/GED + 2 years of work experience, OR
  • Associate's degree and 6 months of work experience, OR
  • Bachelor's degree


Top 3 Must-Have Skill Sets

  • QA experience
  • Knowledge of and hands-on experience handling deviations
  • GMP warehouse knowledge



Nice to Have

  • Warehouse experience



Day-to-Day Responsibilities

Incoming Quality Assurance (IQA) - Inspection, Sampling, and Testing

  • Perform inspections of raw materials (e.g., biobags, tubing, filters, components) to verify compliance with specifications and master inspection characteristics.
  • Execute sampling of media, chemicals, and raw materials in accordance with approved procedures.
  • Perform Raman spectroscopy testing using TruScan equipment to verify material identity.
  • Ensure all inspection, sampling, and testing results are complete, accurate, and documented in compliance with cGMP and GDP (ALCOA) requirements.
  • Evaluate material attributes (e.g., color, appearance, integrity) against defined acceptance criteria.
  • Accurately document results in applicable systems and ensure traceability and data integrity.
  • Assess and escalate characteristics that may impact product quality in accordance with procedures.


Warehouse QA Floor Support (Real-Time Oversight)

  • Provide on-the-floor QA presence to support warehouse operations (receiving, sampling, dispensing, shipping).
  • Perform real-time triage of quality events, discrepancies, and process deviations.
  • Determine immediate containment actions and provide compliant, risk-based guidance to operations.
  • Ensure adherence to GMP requirements, SOPs, and GDP/ALCOA documentation standards.
  • Act as the primary QA point of contact for operational questions and quality-related decision-making.


Deviation, CAPA, and Quality Systems Support

  • Serve as QA contact for deviations, including initiation, classification, and documentation.
  • Ensure timely escalation of critical quality issues to QA leadership.


Inspection Readiness and Continuous Improvement

  • Participate in inspections, walkthroughs, and audit readiness activities.
  • Ensure facilities, equipment, materials, and processes comply with cGMP and safety requirements.



Possible Extension

  • Yes


Red Flags

  • No experience working in a GMP environment.
  • Non-local candidates.
  • Unable to work with chemicals.
  • Unable to stand for the majority of the shift.
  • Unable to occasionally lift up to 50 lbs.


Interview Process

  • Video interview with hiring managers.

Applied = 0

(web-77cf7d65c7-rcc7h)