Senior Quality Assurance Specialist – Pharma

Intellectt INC
  • New York City, NY
  • $50 Per Hour
  • Quick Apply
3 days ago

Job Description

Job Title: Senior Quality Assurance Specialist

Location: New York

Work Type: W2 Contract

Duration: 6+ Months

Experience: 8 10+ Years

Rate: $50 $60/hr W2

Industry: Pharmaceutical / Biotechnology

We are seeking an experienced Senior Pharma QA Specialist to support Quality Assurance and Compliance activities within a highly regulated GMP environment.

Key Responsibilities:

  • Provide senior-level QA oversight for GMP manufacturing and quality operations.
  • Review and support deviations, investigations, CAPAs, change controls, and risk assessments.
  • Ensure compliance with FDA, EU GMP, and applicable regulatory requirements.
  • Support quality systems, validation, documentation, and data integrity activities.
  • Support internal and regulatory audits and inspection readiness.
  • Partner with Manufacturing, QC, Validation, Engineering, and other cross-functional teams.
  • Serve as a QA SME and provide guidance on quality and compliance requirements.

Required Qualifications:

  • 8 10+ years of hands-on QA experience in pharmaceutical, biotechnology, or similarly regulated industries.
  • Strong GMP/cGMP and pharmaceutical quality systems knowledge.
  • Experience with deviations/investigations, CAPA, change control, risk management, and audits.
  • Strong understanding of data integrity and regulatory compliance.
  • Bachelor's degree in Life Sciences, Chemistry, Engineering, Pharmacy, or a related scientific discipline preferred.
  • Strong communication, documentation, problem-solving, and collaboration skills.

Travel Requirement:

  • Must be available to travel to Limerick, Ireland as required.
  • Each visit may require approximately 2 weeks onsite.

Numbers & Facts

LocationNew York City, NY

Skills

  • Auditingunmatched
  • Biologyunmatched
  • Biotech and Pharmaceuticalunmatched
  • Change Controlunmatched
  • Chemistryunmatched
  • Communication Skillsunmatched
  • Corrective and Preventative Action (CAPA) Systemsunmatched
  • Cross-Functionalunmatched
  • Current Good Manufacturing Practice (cGMP)unmatched
  • Data Qualityunmatched
  • Documentationunmatched
  • FDA (Food and Drug Administration)unmatched
  • GMP (Good Manufacturing Practices)unmatched
  • Internal Auditunmatched
  • Maintain Complianceunmatched
  • Manufacturingunmatched
  • Manufacturing Operationsunmatched
  • People Managementunmatched
  • Pharmacyunmatched
  • Problem Solving Skillsunmatched
  • Quality Assuranceunmatched
  • Quality Controlunmatched
  • Regulationsunmatched
  • Regulatory Complianceunmatched
  • Regulatory Requirementsunmatched
  • Risk Analysisunmatched
  • Risk Managementunmatched
  • System Validationunmatched
  • Team Playerunmatched
  • Validation Documentationunmatched
  • Willing to Travelunmatched

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