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The Quality Control Editor reviews and edits clinical documents, regulatory submissions, and publications for accuracy, grammar, and compliance with guidelines. They interpret clinical data as needed and ensure document formatting adheres to templates and style guides. This role requires strong attention to detail and collaboration with the writing team.

The position involves managing Clinical Quality Assurance (CQA) projects, providing consulting, conducting audits, drafting SOPs, and ensuring compliance with GCP, GLP, and GCLP regulations. The role also includes promoting quality programs and addressing regulatory issues for clients.

The CGT/ATMP Senior Consultant will provide expert consultation in quality assurance and regulatory compliance within the cell and gene therapy sector. Responsibilities include auditing, developing Quality Management Systems, providing client training, and ensuring project execution and profitability. The role involves staying updated on regulatory changes and promoting quality services within the industry.

The GVP Auditor will lead clinical consulting and auditing projects, executing audits based on regulatory requirements and GCP/GVP guidelines, while promoting customer satisfaction and compliance. Responsibilities include managing the GVP audit program, supporting clients in compliance issues, generating project proposals, and ensuring alignment with quality principles.