PharmEng Technology
Quality Assurance Specialist
PharmEng Technology, Washington, District of Columbia, us, 20022
About the job Quality Assurance Specialist
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
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