What are the responsibilities and job description for the Quality Assurance Specialist position at PharmEng Technology?
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