I am working with a global pioneer dedicated to the promise of biosimilars who are on their search for a QC Documentation Manager. You will lead a dedicated team responsible for various critical tasks within the QC Department, including data management, LIMS support, sample management, material management of the laboratories, incoming goods sample management, and laboratory equipment lifecycle management

Please note this is a full-time onsite position. The location of this role is confidential until pre-screening has taken place.

You will be responsible for:

• Receiving QC samples, EM plates, and processing QC samples
• Distributing QC samples to QC labs and managing off-site sample shipments
• Develop, revise, and review procedures to ensure best practices
• Managing inventory of lab supplies and materials
• Maintaining cleanliness and organisation in the sample management area
• Reviewing logbooks, sample submission forms, and other QCSM documents
• Performing routine maintenance of lab equipment and lab areas
• Supporting assays, including incubation of EM samples and particle isolation
• Providing effective line management to a team of 18 professionals

You will bring the following:

• SME in LIMS
• Solid line management experience of larger teams within GMP environments
• Hands-on experience in managing samples and QC Documentation
• Must have 5 years working experience in Biologics / Pharmaceuticals / Biopharma