GxP Consultant

Azzur Group is always seeking experienced professionals with a GxP background to join our Consulting Division. Our Consulting Division specializes in guiding clients through the complex landscape of Good Manufacturing Practice (GMP) compliance, ensuring the highest standards of quality and regulatory adherence.

As a GxP Consultant, you will play a pivotal role in collaborating with diverse life sciences companies, leveraging your expertise to provide strategic guidance and support in navigating the regulatory environment.

Apply now, if you have a background in the following areas and want to be a part of a dynamic and innovative life sciences consulting firm dedicated to providing high-quality, compliant solutions to the pharmaceutical, biotechnology, and medical device industries.

• Validation Services: Conduct and oversee validation activities for equipment, processes, and computer systems, ensuring compliance with industry standards and...

Zifo is hiring.. Seeking a highly experienced senior IT professional who can seamlessly hit the ground running in supporting GxP Systems and collaborate cross-functionally with teams such as Quality, Clinical Operations, Pharmacovigilance, and more.

This role entails serving as a GxP IS representative and SME for system implementation and ongoing operations, encompassing access management, access reviews, system administration, risk management, and incident investigations.

You will work alongside the existing Regulated (GxP) Systems staff and Quality as your cross functional partner while providing support and expertise in GxP operations and projects within the realm of information systems.

Requirements

• GxP Computer System administration, support escalation point, and maintenance.
• GxP Computerized System Incident Management and technical investigation.
• Creating SOPs, Guidance Documents, and...

Location: On-Site - Cambridge, MA.
Employment type: Contract

Zifo is seeking a highly experienced senior IT professional who can seamlessly hit the ground running in supporting GxP Systems and collaborate cross-functionally with teams such as Quality, Clinical Operations, Pharmacovigilance, and more.

 This role entails serving as a GxP IS representative and SME for system implementation and ongoing operations, encompassing access management, access reviews, system administration, risk management, and incident investigations.

 As a valued member of the Zifo team and liaison to our pharmaceutical client(s) you will work alongside the existing Regulated (GxP) Systems staff and Quality as your cross functional partner while providing support and expertise in GxP operations and projects within the realm of information systems.

Requirements

Responsibilities:

• GxP Computer System...