QA Operations Specialist - GMP & Compliance (Pharma)

Creative Solutions Services, LLC

Saint Paul (MN)

On-site

USD 70,000 - 95,000

Full time

14 days+
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Job summary

Creative Solutions Services, LLC is seeking a Quality Operations – QA Specialist to support daily QA activities at our client site. You will ensure manufacturing, packaging, and testing operations comply with cGMP and internal quality standards.

Responsibilities include QA review of batch records, deviations, CAPAs, and change controls, and supporting audits, investigations, and documentation. A life sciences degree with 3–5 years in QA or quality operations is required.

Qualifications

  • Bachelor's degree in Life Sciences, Pharmacy, Chemistry, or related field.
  • 3–5 years of experience in Quality Assurance or Quality Operations.
  • Background in Pharma or Healthcare industry is required.
  • Strong understanding of GMP, FDA, and quality systems.
  • Good communication and documentation skills.

Responsibilities

  • Perform QA review of batch records, deviations, CAPAs, and change controls.
  • Provide quality support to manufacturing, packaging, and laboratory operations.
  • Ensure compliance with GMP, FDA, and company quality policies.
  • Participate in investigations and support root cause analysis for quality issues.
  • Review and approve SOPs, validation protocols, and reports.
  • Support internal and external audits and inspection readiness.
  • Maintain accurate QA documentation and records.

Skills

Quality Assurance
Documentation
Communication
Regulatory Knowledge

Education

Bachelor's degree in Life Sciences or related field

Tools

TrackWise
Veeva

Job description

Creative Solutions Services, LLC is seeking a Quality Operations – QA Specialist to support daily QA activities at our client site. You will ensure manufacturing, packaging, and testing operations comply with cGMP and internal quality standards.

Responsibilities include QA review of batch records, deviations, CAPAs, and change controls, and supporting audits, investigations, and documentation. A life sciences degree with 3–5 years in QA or quality operations is required.

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