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Quality Assurance Specialist

PharmEng Technology.com

Office

Washington D.C., District of Columbia, United States

Full Time

Quality Assurance Specialist

Washington, Dc

Contract

Job Description:

Experience: 2-3 years in Quality Assurance (QA) or a strong background in process/manufacturing

  • Industry: Pharmaceutical, GMP environment
  • Responsibilities:
  • Manage documentation processes to ensure compliance with Good Manufacturing Practices (GMP)
  • Handle Corrective and Preventive Actions (CAPA), change control, and deviation management
  • Develop and maintain controlled environments and ensure compliance with industry standards
  • Support the client in managing and streamlining documentation to enhance efficiency and compliance
  • Work towards reducing on-site quality documentation by 80%Collaborate with cross-functional teams to ensure consistent quality standards
  • Skills and Qualifications:2-3 years of experience in Quality Assurance or a strong background in process/manufacturing within the pharmaceutical industry
  • Expertise in documentation management, CAPA, change control, deviations, and complianceStrong understanding of GMP regulations and standards
  • Excellent attention to detail and problem-solving skills
  • Ability to work effectively in a controlled environment
  • Strong communication and interpersonal skills
  • Key Objectives:
  • Reduce 80% of on-site quality documentation
  • Streamline processes to enhance efficiency and compliance
  • Support Client in documentation management

Quality Assurance Specialist

Office

Washington D.C., District of Columbia, United States

Full Time

September 28, 2025

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PharmEng Technology