Kelly

Kelly

Quality Assurance Specialist

Lancaster, SC, United States

Sponsorship not specified$60k-$70kDetected 18 hours ago
ExcelSAPGMPCommunicationCollaborationCritical ThinkingMicrosoft Office

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odds of building a lasting career here

39Risky
Cap-exempt (no lottery)0
Sponsors this role90
Entry-level history0
PERM / green-card track0
Lottery odds (Level I)39
Fits your clock70

Thin sponsorship signal and lottery-bound (~15% per draw). A low-probability bet with your clock running. Prioritize cap-exempt roles and proven entry-level sponsors first.

Lottery odds assume a STEM candidate.

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H-1B wage level

the lottery is wage-weighted — each level is one more entry

Level I · 1×
Level I$63,7731 entry
Level II$79,4772 entries
Level III$95,2023 entries
Level IV$110,9064 entries

The bottom of this range ($60,000) is below the Level I prevailing wage of $63,773. An H-1B cannot be filed below the prevailing wage, so an offer at the floor of this band could not be sponsored as posted.

DOL prevailing wage, 2026-27 wage year · Software Quality Assurance Analysts and Testers (15-1253) · Charlotte-Concord-Gastonia, NC-SC. Wage level is derived by USCIS from the offered wage, occupation and worksite; the occupation shown is inferred from the job title.

Employer immigration record

from this employer's Department of Labor filings

Third-party placement is common here

44% of this employer's visa filings place the worker at a client company rather than at the employer itself, across 17 clients. Your visa, salary band and layoff exposure would follow the employer of record, not the client.Most common: National Institutes of Health · Stryker · Syensqo

Files H-1B transfers

8 transfer filings in the last year, covering 8 workers. Median labor-condition decision: 677 days. An employer that already files transfers is one that can take over an existing H-1B.

Sourced from Department of Labor LCA, PERM and prevailing-wage disclosure data. Employer matching is by name, so figures may be split across an employer's legal entities. Absence of a filing means none appears in our copy of the data, not that none exists.

Community outcomes

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About the role

  • This direct-hire opportunity is ideal for a quality professional with experience in GMP-regulated pharmaceutical or dietary supplement manufacturing who is passionate about compliance, continuous improvement, and product quality.

Responsibilities

  • Support QA activities and quality processes involving Contract Manufacturing Organizations (CMOs).
  • Support Qualityze functions and utilize SAP quality functions as needed.
  • Create and revise SOPs, batch records, process changes, and other GMP documentation.
  • Conduct non-conformance investigations and support root cause analysis.
  • Collaborate effectively with cross-functional teams to support quality and business objectives.
  • Maintain reliable attendance and perform additional duties as assigned.

Nice to have

  • Monday-Friday | 8:30 AM-5:00
  • Provide in-process quality reviews and training to production operators.
  • Assist with quality metrics, trending, and continuous improvement initiatives.
  • Monitor non-conformance reports (NCRs) and Corrective and Preventive Actions (CAPAs) to ensure timely completion and prevent recurrence.
  • Review and release CMO batch records and assist with internal batch releases.
  • Identify and help correct documentation deficiencies in accordance with cGMP, company SOPs, CMO procedures, and applicable global regulations.
  • High school diploma or GED required.
  • Four years of experience in pharmaceutical or dietary supplement manufacturing preferred.

Compensation

  • Competitive salary of $60,000-$70,000 plus bonus potential.

Benefits

  • Comprehensive benefits package.
  • Consistent Monday-Friday schedule year-end leave from December 24 through January 2.

This listing is sourced directly from Kelly's careers page and normalized into a canonical job model.