Proclinical is seeking a dedicated QA Senior to join the Quality Assurance team. This role focuses on ensuring quality throughout the manufacturing and release processes. The successful candidate will be a key quality partner across various departments, ensuring compliance with guidelines and regulatory requirements.
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: Serve as the QA representative for routine GMP activities and projects.
Collaborate with Production Unit Teams, Quality Control laboratories, Warehouse, and Engineering/Maintenance departments.
Ensure the accuracy and compliance of information within systems and documentation.
Participate in GMP audits and shopfloor activities.
Promote and engage in Continuous Improvement initiatives.
Understand and apply EHS guidelines, ensuring personal safety and reporting risks or improvement opportunities.
Act as a backup for other QA Senior Experts and QA Lead as needed.
Key Skills and Requirements: Strong understanding of GMP and regulatory compliance.
Ability to collaborate effectively with cross-functional teams.
Experience in quality assurance within a manufacturing environment.
Commitment to continuous improvement and safety standards.
#J-18808-Ljbffr