Quality Assurance Specialist
Washington, DC
Contract
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
PharmEng Technology, now part of Efor Group, leader in Compliance Engineering, is a leading provider of technical services and solutions to the pharmaceutical, biotechnology, and healthcare industries. With over 25 years of experience, we specialize in Commissioning, Qualification, and Validation (CQV) services for facilities, utilities, equipment, and processes.
As part of Efor’s global network of 3,000 experts across 12 countries, we are better equipped than ever to deliver innovative and comprehensive solutions tailored to the unique needs of clients worldwide. This integration strengthens our ability to combine global expertise with local proximity, positioning PharmEng as a strategic partner for the industry’s most prominent players.
Our team of highly skilled professionals brings a wealth of industry expertise and knowledge to every project, ensuring that our clients receive the highest quality services and solutions. We pride ourselves on our ability to provide flexible, innovative, and cost-effective solutions that meet our clients' unique challenges.
At PharmEng Technology by Efor, we are committed to delivering excellence in everything we do. We work closely with our clients to understand their goals and objectives, developing customized solutions that deliver measurable results. Our focus on quality, safety, and compliance ensures that our clients can trust us to meet their most critical needs.
Specialties: PharmEng Technology specializes in the planning, design, construction, and validation of Health Care, Laboratory, API Pharmaceutical, and Biotechnology facilities and equipment, including computer systems. We provide professional services that meet both regulatory and business demands, following current Good Manufacturing Practices (cGMP), Good Engineering Practices (GEP), and Good Laboratory Practices (GLP).
