Research associate Jobs in Grenchen

Join a dynamic team at a leading Contract Manufacturing Organisation (CMO) and contribute to groundbreaking projects and cutting-edge solutions.

Proclinical is seeking a dedicated QA Associate to join our client's team in Solothurn, Switzerland. In this role, you will provide quality oversight for the review and approval of various validation and engineering lifecycle documents. Your focus will be on ensuring compliance with GMP and regulatory policies during the startup, commissioning, and qualification of a new large-scale manufacturing facility. This position requires collaboration across multiple functions and levels within the organization.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities :

• Oversee the design, build, and qualification of equipment, utilities, and facilities in line with GMP and regulatory standards.
• Review and approve qualification, validation, and engineering documents during project and operational phases.
• Participate in the validation and change control processes for Biogen Execution Systems (BES) at the site.
• Ensure GMP documentation and data comply with applicable procedures and regulatory guidelines.
• Manage QA activities related to protocol deviations, test protocols, change control, and QRMs for equipment and automation systems.

Key Skills and Requirements :