Kedrion Biopharma have a new and exciting opportunity for a motivated and driven Team Leader to join our Quality department (Biohemistry) on-site in Elstree, Hertfordshire.
As a Team Leader, you will lead and support the effective day-to-day delivery of Quality Control activities, ensuring testing, compliance, training, safety and operational priorities are completed to the required standards and timelines. The role provides leadership to the QC team, supports audit readiness, drives continuous improvement, and ensures that quality records, controlled documents, resources and processes are managed effectively to meet business and regulatory expectations.
Each QC Team Leader will have ownership of one specific area of responsibility from the following roles. You will be expected to carry out the above general duties of the Team Leader role as well as the specific requirements of the area assigned. You will be expected to have an understanding of each role, as you may be required to be rotated or reassigned between these different areas as and when operational requirements or business needs necessitate, as well as cover for periods of leave, such as sickness and annual leave.
The initial responsibility for this Team Leader role is - Governance
Responsible for managing departmental stock levels, including reagents, consumables and reference preparations, ensuring materials are available to support testing activities and operational requirements.
Oversee the ordering process and management of critical reagents, while maintaining effective control of Internal Quality Control (IQC) materials, performance trending and stock requirements.
Lead and track Operational Excellence (OE) initiatives, supporting continuous improvement activities and monitoring project progress.
Coordinate departmental training compliance, including method training, health and safety requirements, policies, occupational health assessments and other mandatory activities, ensuring completion within required timescales.
Support health and safety management through action tracking, laboratory inspections, hazard and incident reporting, and maintaining oversight of COSHH and risk assessment reviews.
Provide support for sample approvals, prepare and present Product Quality Review (PQR) reports, and monitor laboratory housekeeping standards to ensure compliance and good laboratory practice.

At Kedrion, we believe that innovation and care must go hand in hand. Our mission is to enhance lives through our dedicated work in the field of rare and ultra-rare diseases.
As a global leader with a passionate team of 5,200 employees, we collect and fractionate plasma to produce and distribute 38 vital medicines worldwide, establishing ourselves as the fifth largest player in the plasma-derived products sector.
What truly sets us apart is our unwavering commitment to every detail, every person, and every interaction. Whether we are engaging with donors, supporting patients, or empowering our employees, we recognize that each connection we make has a meaningful impact. We refer to these as "rare connections," highlighting our belief that every relationship matters.
In partnership with the medical and scientific community, institutions, patient advocacy groups, and research organizations, we drive sustainable innovation that improves patients' lives. Together, we are creating a brighter future for individuals and communities affected by rare diseases.
Join us on this journey as we continue to enhance lives and foster connections that matter. Discover how you can contribute to our mission at Kedrion.