RCI-SNFI-10724 Material compliance Specialist (Third Party Management Specialist)/Veeva- Framingham, MA

This role will work with some of the smaller vendors, reaching out to and working with them. · ...

This role owns key projects across commercial and medical teams, optimizing processes, enhancing platforms, improving efficiency · and compliance. · Lead Marketing Ops projects focused on workflow optimization and system upgrades. · Own content review processes across digital, p ...

This role owns key projects across commercial and medical teams, optimizing processes, enhancing platforms and improving efficiency and compliance. · ...

The Third-Party Management Specialist will oversee Third-Party Quality operations for the MA BioCampus ensuring excellence in quality standards and regulatory compliance across external partnerships. · ...

· This role oversees Third-Party Quality operations for the MA BioCampus ensuring excellence in quality standards and regulatory compliance across external partnerships. · Leading Supplier Change Notification (SCN) processes · , Managing third-party quality event investigations ...

The Third-Party Management Specialist will oversee Third Party Quality operations for the MA Bio-Campus, · ensuring excellence in quality standards and regulatory compliance across external partnerships. · This role requires leading Supplier Change Notification (SCN) processes · ...

The Compliance Specialist II will support manufacturing and quality operations by ensuring compliance with internal procedures GMP requirements and applicable regulatory standards. · Perform audits to ensure manufacturing procedures comply with in-house specifications and governm ...

The Compliance specialist will perform audits to ensure manufacturing procedures comply with in-house specifications and government regulations. · ...

The Compliance Specialist II will support manufacturing and quality operations by ensuring compliance with internal procedures, · GMP requirements, · and applicable regulatory standards.Perform audits to ensure manufacturing procedures comply with in-house specifications and gove ...

This is an onsite role that requires the candidate to perform audits necessary to ensure compliance of manufacturing procedures with in-house specifications and government regulations. · ...

Perform audits necessary to ensure the compliance of manufacturing procedures to in-house specifications and government regulation. · ...

We are looking for Senior Quality Assurance Associate for our client in Framingham, · MA. · The Third Party Management Specialist will oversee Third Party Quality operations · for the MA BioCampus. · This role requires leading Supplier Change Notification (SCN) processes, · manag ...

The Compliance Specialist performs audits to ensure manufacturing procedures comply with regulations. They establish auditing requirements, conduct internal audits, and review testing results. · ...

This is a contract opportunity for a Third Party Management Specialist/Quality Assurance Associate II with long-term potential located in Framingham MA onsite. · ...

We are looking for a talented Compliance Specialist II to join our team at Pyramid Consulting Inc.. As a key member of our quality team you will perform audits necessary to ensure compliance of manufacturing procedures with government regulations. · Key Responsibilities: Perform ...

Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and at scale. · Contribute to the development and implementation of annual training programs to ensure compliance with Good Manufacturing Practices (GMP) and company standards · Evaluate training ef ...

+ Immediate need for a talented Compliance Specialist II (Manufacturing/Quality) 1st Shift. · + This is a contract opportunity with long-term potential located in Framingham, MA. · This Compliance Specialist will perform audits necessary to ensure compliance of manufacturing proc ...

The Third Party Management Specialist will oversee Third Party Quality operations for the MA Bio Campus ensuring excellence in quality standards and regulatory compliance across external partnerships. · This role requires leading Supplier Change Notification SCN processes managin ...

The Clinical Research Associate (CRA) supports the Global Clinical Operations (GCO) Center of Excellence conducting activities consistent with GCOs mission of building a world-class shared clinical technology process innovation and clinical operations team. · IRB submissions and ...

Global Training Specialist responsable for operating and maintaining a compliant Learning Management System (LMS) collaborating with departments to develop training based on needs and role assignments with this regulated environment. · ...