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