CGxPServe

Job Description: We are seeking a Quality Engineer with experience in the medical device industry to support quality assurance regulatory compliance and continuous improvement initiatives. The ideal candidate will have a strong background in FDA regulations ISO 13485 risk management (

Job Description: We are seeking a Quality Engineer with experience in the medical device industry to support quality assurance regulatory compliance and continuous improvement initiatives. The ideal candidate will have a strong background in FDA regulations ISO 13485 risk management (

Responsibilities: The Associate Regulatory Affairs Manager will support the development review and submission of regulatory documents for medical device and IVD products. This role will assist in managing regulatory projects ensuring compliance with FDA ISO 13485 and other global reg

Responsibilities: The Associate Regulatory Affairs Manager will support the development review and submission of regulatory documents for medical device and IVD products. This role will assist in managing regulatory projects ensuring compliance with FDA ISO 13485 and other global reg

Job Description: We are seeking a highly experienced Laboratory Information Management System (LIMS) Subject Matter Expert (SME) with 10 years of proven expertise in the implementation optimization and support of LIMS solutions within clinical and research laboratory environments. Th

Job Description: We are seeking a highly experienced Laboratory Information Management System (LIMS) Subject Matter Expert (SME) with 10 years of proven expertise in the implementation optimization and support of LIMS solutions within clinical and research laboratory environments. Th

Responsibilities: Lead and manage clinical data management activities for oncology clinical trials ensuring adherence to project timelines budgets and quality standards. Provide strategic oversight and direction to CRO clinical data management teams for assigned studies. Develop and

Responsibilities: Lead and manage clinical data management activities for oncology clinical trials ensuring adherence to project timelines budgets and quality standards. Provide strategic oversight and direction to CRO clinical data management teams for assigned studies. Develop and

Job Description: In this role youll ensure manufacturing processes meet quality and regulatory standards while driving improvements across production and compliance. This is a hands-on role with strong cross-functional collaboration and an emphasis on risk management validation and p

Job Description: In this role youll ensure manufacturing processes meet quality and regulatory standards while driving improvements across production and compliance. This is a hands-on role with strong cross-functional collaboration and an emphasis on risk management validation and p

Job Description: Key Focus: FDA experience is highly valued especially if youve led process revamps or redesigned processes reviewed and validated by the FDA. Join a team driving medical device quality and process development bridging compliance requirements and real-world business n

Job Description: Key Focus: FDA experience is highly valued especially if youve led process revamps or redesigned processes reviewed and validated by the FDA. Join a team driving medical device quality and process development bridging compliance requirements and real-world business n

Job Description: Were looking for purpose-driven passionate individuals to join our team. From clinical to commercial to supporting functions Use statistical programming software to develop datasets and tables figures and listings that comply with regulatory standards and support the

Job Description: Were looking for purpose-driven passionate individuals to join our team. From clinical to commercial to supporting functions Use statistical programming software to develop datasets and tables figures and listings that comply with regulatory standards and support the