PharmEng Nordic ApS
Quality Assurance Specialist
PharmEng Nordic ApS, Washington, District of Columbia, us, 20022
About the job: Quality Assurance Specialist
Location:
Washington, D.C.
Scroll down for a complete overview of what this job will require Are you the right candidate for this opportunity Type:
Contract Job Description: We are seeking a Quality Assurance Specialist with 2-3 years of experience in QA or a strong background in process/manufacturing within the pharmaceutical industry. 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 related process/manufacturing role in the pharmaceutical industry. Expertise in documentation management, CAPA, change control, deviations, and compliance. Strong 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 the client in documentation management.
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Location:
Washington, D.C.
Scroll down for a complete overview of what this job will require Are you the right candidate for this opportunity Type:
Contract Job Description: We are seeking a Quality Assurance Specialist with 2-3 years of experience in QA or a strong background in process/manufacturing within the pharmaceutical industry. 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 related process/manufacturing role in the pharmaceutical industry. Expertise in documentation management, CAPA, change control, deviations, and compliance. Strong 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 the client in documentation management.
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